Skip to main content
PMC home page
BMC Plant Biology logoLink to BMC Plant Biology
. 2010 Apr 21;10:73. doi: 10.1186/1471-2229-10-73

Epigenetic chromatin modifiers in barley: IV. The study of barley Polycomb group (PcG) genes during seed development and in response to external ABA

Aliki Kapazoglou 1, Alessandro Tondelli 2, Dimitra Papaefthimiou 1, Helen Ampatzidou 1, Enrico Francia 3, Michele A Stanca 2, Konstantinos Bladenopoulos 4, Athanasios S Tsaftaris 1,5,✉
PMCID: PMC3095347  PMID: 20409301

Abstract

Background

Epigenetic phenomena have been associated with the regulation of active and silent chromatin states achieved by modifications of chromatin structure through DNA methylation, and histone post-translational modifications. The latter is accomplished, in part, through the action of PcG (Polycomb group) protein complexes which methylate nucleosomal histone tails at specific sites, ultimately leading to chromatin compaction and gene silencing. Different PcG complex variants operating during different developmental stages have been described in plants. In particular, the so-called FIE/MEA/FIS2 complex governs the expression of genes important in embryo and endosperm development in Arabidopsis. In our effort to understand the epigenetic mechanisms regulating seed development in barley (Hordeum vulgare), an agronomically important monocot plant cultivated for its endosperm, we set out to characterize the genes encoding barley PcG proteins.

Results

Four barley PcG gene homologues, named HvFIE, HvE(Z), HvSu(z)12a, and HvSu(z)12b were identified and structurally and phylogenetically characterized. The corresponding genes HvFIE, HvE(Z), HvSu(z)12a, and HvSu(z)12b were mapped onto barley chromosomes 7H, 4H, 2H and 5H, respectively. Expression analysis of the PcG genes revealed significant differences in gene expression among tissues and seed developmental stages and between barley cultivars with varying seed size. Furthermore, HvFIE and HvE(Z) gene expression was responsive to the abiotic stress-related hormone abscisic acid (ABA) known to be involved in seed maturation, dormancy and germination.

Conclusion

This study reports the first characterization of the PcG homologues, HvFIE, HvE(Z), HvSu(z)12a and HvSu(z)12b in barley. All genes co-localized with known chromosomal regions responsible for malting quality related traits, suggesting that they might be used for developing molecular markers to be applied in marker assisted selection. The PcG differential expression pattern in different tissues and seed developmental stages as well as in two barley cultivars with different seed size is suggestive of a role for these genes in barley seed development. HvFIE and HvE(Z) were also found to be induced by the plant hormone ABA implying an association with ABA-mediated processes during seed development, germination and stress response.

Background

Epigenetic regulation of gene expression plays a central role in eukaryotic development and takes place through modulation of chromatin structure. Highly organized chromatin consisting of DNA wrapped around histone proteins in nucleosomal structures can switch between relaxed and condensed states associated with transcriptional activity and transcriptional repression, respectively [1]. This is accomplished though cytosine methylation of DNA and post-translational modifications of nucleosomal histone tails. Histone modifications include changes in methylation, acetylation, and phosphorylation on specific lysines and arginines residues. Generally methylation of histone 3 on lysine 9 and 27 (H3K9, H3K27) leads to a repressive chromatin state correlating with gene silencing whereas methylation of histone 3 on lysine 4 (H3K4) leads to a permissive chromatin state correlating with gene activation [2]. Histone acetylation and deacetylation result in active and silent chromatin forms, respectively [3]. This kind of epigenetic regulation operates on various aspects of plant growth and development, including seed formation and stress responses (reviewed in [4,5]).

In flowering plants, the seed is formed through the process of double fertilization. Fertilization of the egg cell by a sperm cell from the male gametophyte generates the diploid embryo from which the organs, tissues and shoot meristems of the plant will be generated. Fertilization of the adjacent central cell by a second sperm cell forms a triploid endosperm, in angiosperms, which supports embryo growth and development by producing storage proteins, lipids, and starch [6].

Bypass of double fertilization is observed in natural apomicts or after mutagenesis of specific gene loci. In Arabidopsis mutations of the FIS (Fertilization Independent Seed) class of genes: FERTILIZATION INDEPENDENT SEED (FIE), MEDEA (MEA), FERTILIZATION INDEPENDENT SEED2 (FIS2), MULTICOPY SUPRESSOR OF IRA1 (MSI1) and BORGIA (BGA), result in the formation of seed-like structures in the absence of double fertilization that eventually collapse [7-9]. The phenotype of fie, mea, fis2 and msi1 mutants is accompanied by another impressive characteristic, that is, endosperm overproliferation [9,10]. Endosperm overproduction and seed size increases are also observed in crosses where extra paternal genomes or hypomethylated maternal genomes are used [11]. Another feature of the fis phenotype is that when the female gametophyte carrying a mutation in a fis locus is fertilized by a wild type plant, the seed finally collapses indicative of a lethal maternal effect of the fis mutation and a gametophytic maternal control over seed development by FIS genes [7,8]. This is partially attributed to parental imprinting of FIE, MEA and FIS2 where only the maternal allele is expressed during the early stages of seed development [12-14].

The common phenotypic effects of the fis mutants are explained by the shared function of the FIS proteins in a PcG complex. The participation of these proteins in a PcG complex was first proposed by [10] and it is now well established that FIE, MEA, FIS2 and MSI1 form the so called FIE/MEA complex, one of the three PRC2 (Polycomb Repression Complex 2) homologues in Arabidopsis, regulating seed formation [15].

The PRC2 complex also known as EXTRA SEX COMBS-ENHANCER OF ZESTE (ESC-E(Z)) complex is one of three PcG complexes in Drosophila. PRC2 has been shown to play a role in the epigenetic silencing of target genes involved in cell growth and proliferation and in early development both in Drosophila and mammals. Its function involves H3K27 methyltransferase activity [16]. Methylation of lysines 9 and 27 of histone 3 serve as epigenetic marks of transcriptional silent loci. The PcG/PRC2 complex in Drosophila contains four essential subunits: two WD40 proteins, named EXTRA SEX COMBS (ESC), and P55 containing the WD40 domain involved in protein-protein interactions, a zinc finger protein, SUPRESSOR OF ZESTE 12 [Su(z)12], and a SET-domain protein responsible for methyltransferase activity, ENHANCER OF ZESTE E(Z) [E(Z)] [17,18].

Different variants of the PRC2 complex have been identified in plants depending on developmental stage, the best studied one being the FIE/MEA complex which regulates the initiation of seed development [18]. It consists of FIE, MEA, FIS2 and MSI1, which are homologous to the Drosophila ESC, E(Z), Su(z)12, and P55, respectively [19,20,13,10]. In Arabidopsis all PcG complexes are predicted to contain the FIE and MSI1 subunits. Depending on cell type and function the different PcG complexes contain one of the three homologues of the Drosophila EZ protein, MEA, CURLY LEAF (CLF) or SWINGER (SWN), and one of the three homologues of the Drosophila Su(z)12 protein, EMBRYONIC FLOWER 2 (EMF2), FERTILIZATION INDEPENDENT SEED 2 (FIS2), and VERNALIZATION2 (VRN2), respectively. The EMF2-CLF/SWN-FIE-MSI1 complex has been suggested to play a role in suppressing the transition from vegetative development to flowering and flower organ formation [15,21] and the VRN2-CLF/SWN-FIE-MSI1 has been implicated in the regulation of the process of vernalization [15,22,23]. EMF2, FIS2 and VRN2, the three Su(z)12-like proteins in Arabidopsis, contain a classical C2H2 zinc finger similar to the fingers found in sequence-specific DNA-binding proteins and another stretch of amino acids, located C-terminal to the zinc finger, that is conserved between DsSu(z)12, HsSu(z)12, EMF2, VRN2 and FIS2 and has been termed VEFS box (VRN2-EMF2-FIS2-Su(z)12 box) [24].

Homologues of the PcG proteins of the FIE-E(Z) complex have been identified in other plant species including monocots, indicating their involvement in a conserved regulatory mechanism among all higher plants [17].

Three target genes for the Arabidopsis FIS2-FIE-MEA-MSI1 complex operating in seed development have been identified so far. The first one is PHERES1(PHE1), a type I MADS box gene [25] which is parentally imprinted in the developing seed, with the maternal allele being silenced and the paternal allele expressed in specialized endosperm cells during the first two days after fertilization [26,27]. The second target is the MEA gene itself, demonstrating an autoregulating mechanism for the imprinting of a PcG epigenetic silencer [28,29]. The third one is FUS3, a transcription factor belonging to the plant-exclusive B3 domain TF family, specifically expressed in seeds during the seed filling phase [30].

Seed development, dormancy and germination are under the control of plant hormones, in particular ABA and gibberellic acid (GA). ABA inhibits germination and is required for the acquisition of dessication tolerance and entry into seed dormancy acting antagonistically to GA during these processes [31,32]. It is also involved in various aspects of plant growth and development including abiotic stress tolerance. Histone modifications have been suggested to play a major role in ABA-mediated processes such as seed development, germination and abiotic stress adaptation [4]. For example, in leaves of Phaseolus vulgaris, externally supplied ABA has been shown to induce methylation of H3K4 and acetylation of H3K14 and H4K5 (indicative of gene activation) of a chromatin region around the phaseolin promoter, and ectopic expression of the otherwise silent in leaves phaseolin gene (encoding a major seed storage protein) [33]. Likewise, ABA-treated seeds of an Arabidopsis mutantof PICKLE (a chromatin remodelling factor mediating suppression of embryonic identity upon germination) showed high expression levels of the ABA-induced transcription factors, ABI3 and ABI5, involved in seed filling. This correlated with reduced H3K9 and H3K27 methylation at ABI3 and ABI5 promoters, in the ABA treated mutant seeds than in wild type seeds [34]. In another study, ABA treatment caused severe reduction in expression of the Arabidopsis histone deacetylase gene, AtHD2C, whereas overexpression of AtHD2C resulted in enhanced abiotic stress tolerance and both repression or induction of several ABA-responsive genes [35]. Recently, ABA was suggested to be a positive regulator of SWI3B, a subunit of the chromatin remodelling complex SWI/SNF, as in Arabidopsis swi3b mutant seedlings exposed to external ABA there was reduced expression of ABA-responsive genes [36]. Furthermore, ABA or an ABA signal was suggested to affect epigenetic states, the DNA replication machinery and chromatin mediated gene expression in Arabidopsis seedlings [37].

Despite the extensive studies on epigenetic regulation of seed development in Arabidopsis, knowledge on epigenetic regulation through DNA and chromatin modulation in cereal seed development is only now starting to emerge. The expression of a large number of genes encoding structural proteins, metabolic enzymes, transcription factors and DNA and chromatin modulators during seed development and germination has been investigated in barley, through large-scale transcriptome analysis [38]. Very recently, as part of our efforts to study epigenetic control mechanisms during seed development in barley, we isolated members of the two families of histone deacetylases, the plant specific HD2 family and the RPD3/HDA1 family as well as members of the histone acetyltransferase families, GCN5, MYST, ELP3, respectively, and investigated their expression at different seed developmental stages, in different grain-size cultivars and in response to external hormonal stimuli [39-41].

Considering the economic importance of cereal crops such as barley, rice, wheat and maize, we report here the characterization of the barley PcG gene homologues. More specifically, a FIE homologue, termed HvFIE, an E(Z) homologue, termed HvE(Z), and two Su(z)12-like homologues, termed HvSu(z)12a and HvSu(z)12b, respectively, were characterized. The mapping position of HvFIE, HvE(Z), HvSu(z)12a, and HvSu(z)12b on different barley chromosomes was assigned, and their expression was examined in different tissues and seed developmental stages and in barley cultivars which differ in seed size and weight. Furthermore, the expression of HvFIE, HvE(Z) and HvSu(z)12b was investigated after treatment with the plant hormone ABA, a modulator of gene expression during developmental and environmental changes, operating often through epigenetic modifications of target genes.

Methods

Plant material

Commercial barley cultivars, Caresse, Carina and Ippolytos, differing in seed size and weight were planted in the field and were the source of RNA for expression analysis. For Caresse, the weight of 1000 grains is 50-55 gr, and 98% of seeds have diameter longer than 2.5 mm, for Carina the weight of 1000 grains is 36-40 gr and 60-65% of seeds have diameter longer than 2.5 mm whereas for Ippolytos, seeds weigh 25-31 gr per 1000 grains and only 35-45% of seeds have diameter longer than 2.5 mm http://www.cerealinstitute.gr. The Oregon Wolfe Barley Dominant (OWB-D), Oregon Wolfe Barley Recessive (OWB-R), L94 and Vada parental barley lines were used for polymorphism detection and mapping.

Hormonal treatment

Seven-day-old seedlings (Caresse) grown in a growth chamber (16 hours (h) light, 8 h darkness, at 22°C) were sprayed with 100 μM ABA, (abscisic acid +/- cis, trans-ABA, SIGMA). Aerial parts of plants were collected at 6 h and 24 h after treatment and immediately stored in liquid nitrogen. Aerial parts from five plants were pooled together for RNA extraction for each time point. Control plants were sprayed with water plus 0.2% Tween.

Identification of barley PcG gene homologues and protein analysis

The barley FIE and E(Z) homologues were identified by searching the barley EST database at the TIGR Web site http://www.tigr.org. Blast searches were performed using the complete cDNA sequence of Arabidopsis FIE, MEA, FIS2. Two tentative consensus sequences of barley ESTs in the TIGR web site, TC134355 and TC140937, were identified, coding for genes which are homologous to the Arabidopsis FIE and MEA, respectively. A blastn search on the NCBI Web site http://blast.ncbi.nlm.nih.gov/Blast.cgi using TC140937 identified a full length E(Z) mRNA sequence (AK251149) from the BARLEY DB http://www.shigen.nig.ac.jp/barley/. Three complete mRNA sequences encoding Su(z)12-like homologues were identified in GenBank with accession numbers AB085817, AB085818, AB085819, respectively. Homology searches were performed with a BLAST algorithm [42] against the DDBJ/EMBL/GenBank database. Sequence alignments were generated with the Clustal W Method [43] of MegAlign (LaserGene software) and processed with the Bioedit software. The sequences and accession numbers used for protein sequence analysis are shown in Table 1. The phylogenetic tree was calculated using MEGA 3.1 software [44] by the Neighbor-Joining Method with p-distance correction [45]. For E(Z), the Bayesian inference of phylogeny was applied with the use of MrBayes 3.1.2 [46]. Four Metropolis-coupled Markov chain Monte Carlo chains were run on one million generations, with sampling every 100 generations. After discarding the first 5,000 unstable trees as burn-in, a majority-rule consensus tree was visualized and edited with TreeView 1.6.6 [47].

Table 1.

Protein sequences used for alignments and phylogenetic tree construction.

Organism name Gene name Accession number
Arabidopsis thaliana AtFIE AF129516
Catalpa speciosa EgrFIE AY150282
Eucalyptus grandis CspFIE AY150283
Hordeum vulgare HvFIE TC134355
Oryza sativa nipponbare OsnFIE2 BAD03073
Oryza sativa japonicum OsjFIE BAD03075
Sorghum bicolor SbiFIE1 AAS82595
Sorghum bicolor SbiFIE2 AAS82596
Zea mays ZmFIE1 AY061964
Zea mays ZmFIE2 AY061965
Arabidopsis thaliana AtSWN NP_567221
Arabidopsis thaliana AtCLF1 AAC23781
Arabidopsis thaliana AtMEA AAC39446
Hordeum vulgare HvEZ AK251149
Oryza sativa indica OsiEZ1 BAD69169
Oryza sativa japonicum OsjEZ CAD18871
Petunia hybrida PhCLF1 BAC84950
Petunia hybrida PhCLF2 BAC84951
Petunia hybrida PhCLF3 BAC84952
Triticum monococcum TmEZ ABI94364
Zea mays MEZ1 AF443596
Zea mays MEZ2 AF443597
Zea mays MEZ3 AF443598
Arabidopsis thaliana AtEMF2 BAB58956
Arabidopsis thaliana AtIEMF2-isoform Q8L6Y4-2
Arabidopsis thaliana AtFIS2, ABB84250
Arabidopsis thaliana AtFIS2b AAD09104
Arabidopsis thaliana AtVRN2 AAL32135
Dendrocalamus latiflorus DendrEMF2 ABB77210
Hordeum vulgare HvSu(z)12a (HvEMF2a) BAD99130
Hordeum vulgare HvSu(z)12b (HvEMF2b BAD99131
Hordeum vulgare HvSu(z)12c (HvEMF2c) BAD99132
Oryza sativa OsEMF AAQ84239
Oryza sativa japonica OsVEF AP005912
Oryza sativa OsEMF-like Q7XSN0
Triticum aestivum TmEMF AY887064
Yucca filamentosa YfEMF2 ABD85300
Zea mays ZmEMF2-like (VEF101) AAO84022
Zea mays ZmEMF-like ABC69154
Drosophila melanogaster DmSu_z_12 AAF73149
Mus musculus MmSu(z)12 BAC65495
Homo sapiens HsSu(z)12 BAA09931
Open in a new tab

Mapping of barley PcG genes

Genomic DNAs extracted from 94 'OWB-Dominant' x 'OWB-Recessive' [48] doubled haploid lines and from 103 'L94' x 'Vada' [49] recombinant inbred lines were used for linkage analyses. Specific PCR primer pairs were designed based on the nucleotide sequences of the PcG genes by using the software Primer3 [50] (Table 2). PCR amplifications were performed in a 20 μl final volume containing: 40 ng of genomic DNA as template, 1× Promega PCR buffer, 1.5 mM of MgCl2, 5% DMSO, 0.25 mM of each dNTP, 0.4 μM of each primer, and 1 U of Taq DNA Polymerase (Promega, Madison USA). Reactions were incubated for 2 min at 94°C, followed by 40 cycles of 94°C for 30 s, 55°C for 30 s, 72°C for 1 min, and a final extension of 72°C for 7 min. PCR products were purified using the Wizard SV Gel and PCR Clean-Up System (Promega, Madison USA), and sequenced on both strands to confirm their identities, then sequences were aligned using the Staden package http://staden.sourceforge.net to identify Single Nucleotide Polymorphisms (SNPs). Inspection of the restriction enzyme cleavage sites with the software WebCutter http://www.firstmarket.com/cutter) revealed HindIII and DdeI restriction enzyme cleavage polymorphisms in the sequenced HvE(Z) and HvSu(z)12a PCR products, respectively. For HvSu(z)12b and HvFIE sequence polymorphisms identified between the mapping parents were not within restriction sites, so PCR markers were made by introducing a restriction site (RsaI and DdeI, respectively) into the PCR product using the dCAPS strategy [51]. According to manufacturer's instructions, 5 μl of PCR product were incubated for 1.5 h with 1 U of the corresponding restriction enzyme, 1× reaction buffer and 0.1 mg/ml of bovine serum albumin, and then separated on a standard 2% agarose gel. The positions of the genes in the barley genome have been determined with high resolution by integrating the new PcG data with data that are publicly available. Linkage analysis was performed with the software JoinMap 4.0 [52] by adding the HvFIE and HvEZ markers to the 'OWB-D' x 'OWB-R' map [53], http://wheat.pw.usda.gov/ggpages/maps/OWB), and the HvSu(z)12a and HvSu(z)12b markers to the 'L94' x 'Vada' map [49], http://wheat.pw.usda.gov/report?class=mapdata&name=Barley,+L94+x+Vada,+2006).

Table 2.

Primers used for expression analysis and mapping.

Gene Primer Sequence (5'-3') Tm (°C) Fragment (bp)
Expression
HvFIE HvFIE F1 GTGCCCGATTGTGACATTTGGTTT 70 264
HvFIE R1 CACGGCGGTTTTTGCTTCCTTC 68
HvE(Z) HvE(Z) F1 AAGCATCTGGTTCTCATCGTC 62 293
HvE(Z) R1 TGGTCCACCTCAACAAGTAGA 62
HvSu(z)12a HvSu(z)12a F1 TCGTGACTCGGTAGGAAACATTG 68 261
HvSu(z)12a R1 CCAATGTTAATAGGTGTTTCAAG 62
HvSu(z)12b HvSu(z)12b F1 GTATATGAGTTGAGCATAGTGC 62 278
HvSu(z)12b R1 TTCAGATGGATTTCATTACAGC 60
HvSu(z)12c HvSu(z)12c F ATGTGCCGTCAACCGTCCACG 68 463
HvSu(z)12c R CTCCAGCTTGCCCTTGTGAAG 66
HvActin Barley Actin F ATGGCTGACGGTGAGGACATCCAGCC 72 1111
Barley Actin R TCAGAAGCACTTCCTGTGGACGATCGC 71
HvActin F GCCGTGCTTTCCCTCTATG 60 235
HvActin R GCTTCTCCTTGATGTCCCTTA 62
HVA22 HVA22 F TGGCGCTCCCGCAGTTCAAG 64 123
HVA22R CCTTGAGTATGTGCACCTTGTG 62
Mapping
HvFIE HvFIE F2 GTGGGAGCCAAAAACAAAAG 60 262
HvFIE R2 GGCGTCACAGGCTAAGTAAGG 61
HvE(Z) HvE(Z) F2 AAATCAGATGTTGCAGGATGG 60 550
HvE(Z) R2 GCTCCCTTGCATAGATACCAAC 61
HvSu(z)12a HvSu(z)12a F2 ACTCGTGCAGAACCCAAGAC 60 576
HvSu(z)12a R2 ACCCATCCCAGCTACAACAG 60
HvSu(z)12b HvSu(z)12b F2 ATATTCCTTGGGCCTGTGAG 59 308
HvSu(z)12b R2 TGGAACAGAACACGACGAAG 54
Open in a new tab

RNA isolation and first strand cDNA synthesis

Total RNA was isolated from roots, shoots, apical meristems, first leaves of seedlings, pistils, stamens, whole flowers before fertilization (immature flower, IMF), seeds 1-3, 3-5, 5-10, 10-15 days after flowering (DAF), and aerial parts after hormonal treatment, respectively, using TRI REAGENT (SIGMA) according to the instructions of the manufacturer. First strand cDNA synthesis was performed using 1.0 μg total RNA, 0.5 μg 3' RACE Adapter primer 5'-GGCCACGCGTCGACTAGTAC (T)17-3' (Invitrogen), 1 mM dNTPs and 200 U M-MuLV reverse transcriptase (Invitrogen,) in 20 μL total volume, according to the specifications of the manufacturer.

Expression analysis of barley PcG genes

Qualitative RT-PCR was used for examining the expression of the HvFIE, HvE(Z), HvSu(z)12a, HvSu(z)12b and HvSu(z)12c barley homologues in different tissues. cDNAs produced from 1 μg of total RNA from roots, shoot meristems, young shoots, leaves, stamens, and pistils before fertilization from a medium-seed-size cultivar, Carina, were used. The primer pair Barley Actin F/Barley Actin R, amplifying a 1111 bp fragment of the barley actin coding gene [AY145451], was used as internal control for successful cDNA synthesis. The PCR conditions for actin were: initial denaturation at 94°C for 3 min, then 30 cycles at 94°C for 30 s, 70°C for 1 min, 72°C for 2 min and final extension at 72°C for 15 min. The PCR conditions for the HvFIE were: initial denaturation at 94°C for 2 min, then 30 cycles of 94°C for 30 sec, 53°C for 30 sec, 72°C for 40 sec and final extension at 72°C for 10 min. The same thermocycler program was used for the fragment amplification of the other four genes, except for the annealing step which was 57°C for HvE(Z), HvSu(z)12b, and HvSu(z)12a, and 62°C for HvSu(Z)12c respectively.

Quantitative real-time RT-PCR was performed with cDNA synthesized from 1 μg of total RNA from immature flowers, seeds 1-3 DAF, 3-5 DAF, 5-10 DAF, and 10-15 DAF from Caresse and Ippolytos, respectively, and aerial parts of Caresse seedlings after ABA treatment. For each sample a reaction was set up in a PCR reaction mix (20 μl) containing 5 μl of the 1:200 diluted cDNA, 0.25 μM of each primer and 1× Platinum SYBR Green qPCR Supermix-UDG (Invitrogen, Paisley, UK) and using an Opticon 2 (MJ Research, Waltham, MA) real-time PCR system and the Opticon Monitor 3 software package (MJ Research). Each reaction was performed in triplicates. General thermocycler conditions were 50°C for 2 min, 95°C for 2 min, then 42 cycles of 95°C for 30 sec, annealing [HvE(Z): 56°C; HvFIE: 57°C; HvSu(z)12b: 54°C, respectively] for 30 sec, 72°C for 30 sec, then 72°C for 5 min and plate read at 82°C. To identify the PCR products a melting curve was performed from 65°C to 95°C with observations every 0.2°C and a 10-s hold between observations. Relative quantification and statistical analysis were performed with the REST software [54] and using actin as the reference gene with HvActinF/HvActinR as primers. The barley gene HVA22, which is known to be induced by ABA [55] was used as a positive control. All primers used in expression analysis correspond to non-conserved regions and are shown in Table 2.

Results

Identification of barley PcG gene homologues and analysis of putative proteins

A blast search of the Hordeum vulgare EST database in TIGR http://www.tigr.org detected an EST (TC134355) corresponding to FIE and an EST (TC140937) corresponding to E(Z), respectively. TC134355 contains a full length cDNA sequence (1623 nt translating to 378 aa) of a barley FIE homologue, which we termed HvFIE. Amino acid sequence alignment of plant FIE homologues revealed that the HvFIE putative protein belongs to the highly conserved FIE family and that it contains the seven characteristic WD40 repeats (Figure 1).

Figure 1.

Figure 1

Open in a new tab

Alignment of the amino acid sequences of the FIE homologues in different plants. The sequences and accession numbers used for protein sequence analysis are shown in Table 1. Identical and similar amino acid residues are shaded in dark grey and light grey, respectively. WD 40 repeats are marked above the sequences with grey lines.

TC140937 contains a partial cDNA sequence (1151 nt) corresponding to a barley E(Z) homologue which we termed HvE(Z). A tblastn search with this sequence revealed a full length mRNA sequence (AK251149) from the BARLEY DB http://www.shigen.nig.ac.jp/barley/ which contains 3092 nt encoding 884 aa of an E(Z) homologue. The putative E(Z) protein from barley, HvEZ, contains the characteristic SET-domain and the cysteine-rich region as shown in the alignment of the E(Z) amino acid sequences from different organisms (Figure 2). The barley protein has 94% identity with the E(Z) protein from wheat (TmEZ), and 70% identity with the EZ2 and EZ3 proteins from maize (MEZ2, MEZ3).

Figure 2.

Figure 2

Open in a new tab

Alignment of the amino acid sequences of the E(Z) homologues from different plants. Sequences and accession numbers are shown in Table 1. Identical and similar amino acid residues are shaded in dark grey and light grey, respectively. The cysteine rich domain and the SET-domain are shown above the sequences with hatched and gray lines, respectively.

A search in GenBank identified three complete mRNA sequences from barley coding for Su(z)12-like homologues with accession numbers AB085817, AB085818, and AB085819 which we named HvSu(z)12a, HvSu(z)12b, and HvSu(z)12c, respectively. These sequences encode putative proteins of 660 aa, 637 aa, and 460 aa, respectively. They all contain the characteristic zinc finger domain found in VEFS proteins, and the HvSu(z)12a, HvSu(z)12b putative proteins also contain the conserved VEFS domain as shown in the VEFS protein alignment (Figure 3). The HvSu(z)12c amino acid sequence terminates before the VEFS domain but this could be due, in part, to a sequencing problem at the 3' end of the particular cDNA as the nucleotide sequence of AB085819 contains unexplained repeats. Because of this problem we decided not to study HvSu(z)12c any further. HvSu(z)12a and HvSu(z)12b share 58% identity with each other. HvSu(z)12b is highly similar to a wheat EMF protein TaEMF, with 93% identity.

Figure 3.

Figure 3

Open in a new tab

Alignment of the amino acid sequences of Su(z)12 protein homologues from different plants. Sequences and accession numbers are shown in Table 1. Identical and similar amino acid residues are shaded in dark grey and light grey, respectively. The Zinc-finger domain and the VEFS box are indicated by hatched and gray lines, respectively.

A phylogenetic analysis of FIE homologues in plants showed that HvFIE is more closely related to other cereal FIE proteins, specifically, ZmFIE2 from maize and OsnFIE2 from rice (Figure 4A). Similarly, phylogenetic analysis of E(Z) proteins from monocots and dicots showed that HvEZ groups out together with TmEZ, MEZ2, MEZ3 and OsiEZ1, whereas AtCLF, MEZ1, OsjEZ form another cluster and AtSWN and AtMEA are more distant to both groups (Figure 4B). A phylogenetic analysis of various VEFS proteins from different organisms (Figure 4C) showed that HvSu(z)12b is more closely related to EMF proteins from wheat, dendrocalamus, oryza and maize, whereas HvSu(z)12a forms a cluster with two other EMF proteins from rice. They are both more distantly related to the Arabidsopsis EMF, FIS2, and VRN proteins and their isoforms, and from the animal Su(z)12 homologues (Drosophila, mouse, and human) which cluster together.

Figure 4.

Figure 4

Open in a new tab

Phylogenetic analysis of PcG proteins. Phylogenetic trees of PcG homologues from different organisms. A) FIE. B) E(Z). C) Su(z)12. Barley sequences are in bold. Sequences and accession numbers are shown in Table 1.

Mapping of barley PcG genes

HindIII cleaved amplified polymorphic sequence (CAPS) and DdeI derived cleaved amplified polymorphic sequence (dCAPS) markers were developed for the mapping of HvE(Z) and HvFIE on the OWB molecular linkage map, respectively. Linkage analysis revealed that HvE(Z) maps in a cluster of 43 molecular markers in the centromeric region of chromosome 4H, and HvFIE co-segregates with RFLP marker MWG808 and other 52 markers in the pericentric region of chromosome 7H (Figure 5). CAPS (DdeI) and dCAPS (RsaI) marker segregation analyses were performed for mapping HvSu(z)12a and HvSu(z)12b on the LxV linkage map. HvSu(z)12a and HvSu(z)12b are located on the short arm of chromosome 2H and on the subcentromeric region of the long arm of chromosome 5H, respectively (Figure 5).

Figure 5.

Figure 5

Open in a new tab

Mapping of barley PcG genes. Chromosomal position of barley HvE(z) and HvFIE genes on the OWB molecular linkage map and HvSu(z)12a and HvSu(z12)b on the LxV molecular linkage map. Only non co-segregating markers are reported, with distances in Kosambi cM. The BIN where each PcG gene has been mapped is indicated following the notation of [49] that integrates data from 6 segregating populations including both the OWB and the LxV maps.

Differential expression of barley PcG genes in different tissues and seed developmental stages and in two cultivars with varying seed size

Qualitative RT-PCR was performed in order to examine the expression of HvFIE, HvE(Z), HvSu(z)12a and HvSu(z)12b in different tissues, in a medium-seed-size cultivar, Carina (Figure 6A). The HvFIE mRNA is abundant in shoot meristems, young shoots, pistils before fertilization and seeds of 1-2 DAF and 3-5 DAF, whereas it is hardly detectable in roots, leaves and stamens. The HvE(Z) transcript is abundant in young shoots and 3-5 DAF seeds, moderate in the other tissues, and detectable in stamens. The HvSu(z)12b transcript is abundant in young shoots, at moderate levels in 1-2 DAF seeds and at low levels in the other tissues. The HvSu(z)12c transcript is abundant in young shoots, present at moderate levels in leaves, at low levels in seeds 1-2 DAF and 3-5 DAF and undetectable in the other tissues examined, whereas the HvSu(z)12a transcript is undetectable in all tissues examined except from young shoots where a very faint band is observed.

Figure 6.

Figure 6

Open in a new tab

A) Qualitative RT-PCR expression analysis of barley PcG genes. R, roots; M, meristem; L, Leaves; YS, young shoots; St, stamens; Pi, unfertilized pistils; 1-2, 1-2 DAF; 3-5, 3-5 DAF; HvActin, was used as the internal control. Cultivar was Carina (a medium-grain cultivar). DAF, Days after fertilization. B) Quantitative real-time RT-PCR analysis of PcG >genes. Expression values were normalized to those of HvActin. The relative expression ratio of each sample is compared to the control group which was C5 (Caresse immature flowers). C, cultivar Caresse, (white bars); IP, cultivar Ippolytos (grey bars). 5, Immature flower; 6, Seed 1-3 DAF; 7, Seed 3-5 DAF; 8, Seed 5-10 DAF; 9, Seed 10-15 DAF. Data represent mean values from two independent experiments with standard deviations. Values significantly different (P < 0.05) from the control group (C5) are marked with an asterisk.

Quantitative real-time PCR was performed in order to compare the levels of HvFIE, HvE(Z), and HvSu(z)12b mRNA accumulation at different stages of seed development and between two barley cultivars with different seed size, Caresse (larger seed size) and Ippolytos (smaller seed size) (Figure 6B). HvSu(z)12a was not included in this analysis, owing to its negligible expression. Similarly, HvSu(z)12c was excluded due to undetectable or low expression in reproductive tissue and seed, respectively.

HvFIE mRNA accumulation exhibits an increase after fertilization, in both Caresse and Ippolytos. In Caresse HvFIE transcript levels reach a maximum at 3-5 DAF (C7) with approximately a 5 fold increase as compared to immature flowers (C5) and decrease thereafter to about 50% in 10-15 (C9) DAF. Conversely, in Ippolytos, HvFIE exhibits a continuous induction with a pronounced increase up to 7 fold at 10-15 DAF (IP9) as compared to immature flowers (IP5). At 5-10 DAF and at 10-15 DAF, HvFIE transcript levels are markedly higher in Ippolytos (approximately 1.5 and 3.5 fold, respectively) as compared to Caresse (Figure 6B).

HvE(Z) transcript levels decline after 1-3 DAF (C6) in Caresse, with maximum decrease in 3-5 DAF (2 fold reduction as compared to immature flowers) whereas comparable decrease was not observed in 3-5 DAF (IP7) for Ippolytos. Contrary to Caresse, HvE(Z) expression levels in Ippolytos do not show any significant changes in any of the stages before fertilization and throughout seed development.

HvSu(z)12b transcript levels are increased after fertilization at the stages 5-10 and 10-15 DAF as compared to immature flowers, both for Caresse and Ippolytos. No significant differences are observed among immature flowers, 1-3 DAF and 3-5 DAF, in either cultivar, and HvSu(z)12b levels are comparable between cultivars throughout seed development.

Expression analysis of barley PcG genes after treatment with ABA

Quantitative real time PCR was performed using total RNA from seven-day-old seedlings subjected to exogenous ABA (100 μM) to examine whether HvFIE and HvE(Z) respond to this seed developmental and stress-related hormone (Figure 7). HvFIE showed a striking 10 fold induction at 24 h after ABA spraying of seven-day-old seedlings, as compared to the untreated plants. HvE(Z) showed a marked induction of approximately 4 fold, both at 6 h and 24 h after ABA treatment, as compared to the untreated control. Expression of HvSu(z)12b did not show any significant changes after ABA treatment (data not shown).

Figure 7.

Figure 7

Open in a new tab

Expression analysis of barley PcG genes after treatment of seedlings with ABA. Quantitative real-time PCR analysis of HvFIE and HvE(Z) genes at 6 and 24 h after treatment of Caresse seedlings with 100 μM ABA. Expression values were normalized to those of HvActin. Data represent mean values from two independent experiments with standard deviations. Relative expression ratio of each sample was compared to the control group which was untreated plants, 0 h, and was assigned the value of 1. Grey bars, hormone-treated plants for 6 h and 24 h; white bars, no hormone treated plants (mocked with H2O/Tween for 6 h and 24 h, respectively). Values significantly different (P < 0.05) from the control group are marked with an asterisk. The barley gene HVA22 (known to be induced by ABA) was used as positive control.

Discussion

In the current study we present the identification, mapping and expression profiles of the genes encoding PcG chromatin modifiers from barley. This work serves as a first step in understanding the role played by PcG genes in the epigenetic mechanisms that control seed formation and stress response in a monocot cereal plant. Unlike dicots, where the endosperm is consumed by the embryo during seed maturation, in monocots such as cereals, the endosperm persists after embryo development is completed and constitutes the major portion of the mature kernel [6,7]. The endosperm of cereal crops like barley, wheat, rice, maize, stores reserves such as proteins, starch, and fatty acids, and represents 60% of the world's food and feed supply. Consequently, understanding and manipulating the molecular mechanisms governing endosperm development for increasing seed yield is of utmost interest for agriculture.

Four barley PcG gene homologues encoding the putative PcG proteins HvFIE, HvEZ, HvSu(z)12a and HvSu(z)12b were identified and analyzed. In Arabidopsis the respective PcG counterparts are [AtFIE], [AtMEA or AtSWN or AtCLF] and [AtFIS2 or AtEMF2 or AtVRN2]. Three different PcG complex variants can be formed depending on the different combinations of these subunits. The changeable subunits are the MEA and FIS2 homologues whereas FIE is likely to be common in all three complexes. The FIE, MEA, FIS2 proteins form a complex essential for viable seed formation. MEA, CLF, and SWN, constitute the three Arabidopsis E(Z) homologues, which cluster into three separate clades, and are members of different PcG complexes with distinct functions. MEA is important for proper seed development and SWN acts redundantly with MEA having a role in preventing endosperm development as well [56]. However according to another report by Spillane et al. 2007 [57], swn/clf double mutants in Arabidopsis produce normal seeds suggesting that neither SWN nor CLF has a role in seed formation. In addition, SWN and CLF are involved in the vernalization process [23]. It was proposed that these homologues have arisen through an old duplication and separation of CLF from the MEA/SWN lineage, which occurred before the divergence of monocots and dicots, whereas a more recent duplication produced the separation between MEA and SWN in only a few species [57]. No direct orthologues of MEA have been found in any other species than Arabidopsis. E(Z) homologues identified in maize and rice [58-60], two monocots with sequenced genomes, cluster in two clades: ZmMEZ2, ZmMEZ3 and OsiEZ1 form the so-called SWN-like clade, and ZmMEZ1 and OsjEZ (also named OsCLF) form the CLF-like clade. Phylogenetic analysis showed that the barley homologue HvEZ is a close relative of the wheat, rice and maize E(Z) homologues belonging in the SWN-like clade. Unlike Arabidopsis, which has at least three E(Z) homologues functioning at different stages of the plant's life cycle, a second HvEZ homologue has not been identified in barley as yet. It might be possible that HvEZ is a common member of the different PcG complex variants that may be operating at different stages of barley development. However, this hypothesis awaits sequencing of the barley genome and further experimentation. In the absence of a MEA counterpart it is possible that the role of MEA is played by one of the putative SWN or CLF homologues both in barley and in the other species lacking MEA.

HvFIE maps on chromosome 7Hcen which is colinear with rice chromosome 8, where the rice OsnFIE2 homologue (Os08g04270) has been also localized. HvE(Z) maps on chromosome 4Hcen which is colinear with rice chromosome 3, where the rice OsiEZ1 homologue (Os03g19480) is found [60]. Similarly, HvSu(z)12a maps on chromosome 2Hshort which is colinear with rice chromosome 4, where the OsEMF (Os04g08034) homologue is localized, and HvSu(z)12b maps on chromosome 5Hlong which is colinear with rice chromosome 9 where the rice homologue OsVEF (Os09g13630)is localized [60]. These observations are in agreement with the extensive synteny between barley and rice chromosomes.

HvFIE and Hv(E)Z are located in the centromeric region of chromosome 7H and 4H repectively, where important clusters of malting quality QTLs have been identified by several authors and reviewed by [61]. Noteworthy, using the Oregon Wolfe Barley map [53] that integrates 2383 loci and a comprehensive summary of 154 QTLs of malting quality http://wheat.pw.usda.gov/ggpages/maps/OWB/, it is possibile to relate the high resolution genomic location of the two PcG genes with historical QTL data. Hv(E)Z location is coincident with scind03751 and 1.1 cM proximal to Tef2, the significant marker for the beta-Glucanase activity QTL (QBgsg.StMo-4H) identified in the Steptoe x Morex population. HvFIE maps to a cluster of OPA and DArT markers that includes MWG808 and is 10 cM proximal to MWG2031, the significant marker for both Grain protein content (QGpc.HaMo-7H) and Kernel plumpness (QKp.HaMo-7H) in the Harrington x Morex population.

Likewise the map position of the two Su(z)12 homologues (HvSu(z)12a on the short arm of chromosome 2H and HvSu(z)12b close to the centromere of chromosome 5H), is in proximity to genomic regions historically involved in the genetic control of malting quality traits [61]. However, all these gene-QTL relationships cannot be unequivocally established and thus further research is needed to determine the role of PcG in endosperm-related traits.

Qualitative RT-PCR analysis demonstrated that the barley HvFIE shows a tissue expression profile similar to that of AtFIE, maize ZmFIE2 and rice OsFIE2 [13,62,58,63,60] in that it is expressed in both vegetative and reproductive tissues. Similarly, the barley HvE(Z) is expressed throughout development like the maize homologues ZmMEZ1, ZmMEZ2 and ZmMEZ3 [58] and the rice E(Z) homologues, OsiEZ1 and OsCLF (same as OsjEZ) [60], whereas AtMEA is not expressed in leaves [19,12,64]. The expression pattern of HvSu(z)12b is similar to the rice OsEMF homologues, being expressed both in vegetative and reproductive tissues [60]. Conversely, AtFIS2 is expressed only in the central cell and endosperm [13]. No expression studies on the maize Su(z)12 homologues, ZmEMF-like and ZmEMF2-like, have been reported so far. The differential expression of AtMEA and AtFIS2 compared to E(Z) and Su(z)12 homologues from monocots and other dicots, together with the fact that the protein sequences of AtMEA and AtFIS2, are distantly related to the E(Z) and Su(z)12 homologues from cereals and other dicots supports the view proposed by Luo et al. 2009 [60], that the MEA and FIS2 genes arose only within the Brassicaceae.

In Arabidopsis, mutations in the PcG genes resulting in downregulation of AtMEA, AtFIE and AtFIS2, cause seed-like structure formation in the absence of fertilization and the production of non-viable seeds after fertilization. In both cases endosperm overproliferation has been observed. Endosperm overproliferation could be a desirable feature of viable and qualitatively acceptable seeds in crops where the seed and in particular the endosperm is the agronomically important product. In this study we attempted to analyze quantitatively the expression of the PcG gene homologues in different seed developmental stages and in two barley cultivars differing in seed size, in order to unravel any association between the expression of these genes with seed development and the size of seed. Quantitative real time PCR expression analysis revealed a differential expression pattern during seed development and significant differences between two barley cultivars with varying seed size for the PcG genes. HvFIE exhibits a pronounced increase after fertilization for both cultivars, which declines in Caresse after 3-5 DAF, but increases remarkably in Ippolytos (approximately 7 fold) at 5-10 and 10-15 DAF. Interestingly, HvFIE transcript levels are markedly higher in Ippolytos at 5-10 and 10-15 DAF than in Caresse by approximately a factor of 1.5 and 3.5, respectively. HvE(Z) expression shows a decline in Caresse seeds 3-15 days after fertilization as compared to flowers prior to fertilization, with a marked 2 fold decrease at 3-5 DAF. Conversely, such a reduction is not observed in Ippolytos, where HvE(Z) transcript levels do not show any significant changes among seed stages. In barley, endosperm cellularization begins at approximately 4 DAF and ends at 6-8 DAF, when the seed maturation process begins [6]. It might be possible that the differences in HvE(Z) and HvFIE expression between the two cultivars during these critical stages of endosperm development are associated with the processes of cellularization and seed filling and ultimately with the size of seed. For HvSu(z)12b, transcript levels show an induction after fertilization at 5-10 and 10-15 DAF, implying a role for HvSu(z)12b in the cellularization and seed maturation process for both cultivars. Further experiments will be needed to elucidate the precise roles of these PcG genes in barley seed development.

The plant hormone ABA, is involved in various plant developmental processes, including seed development, germination and abiotic stress tolerance. In Arabidopsis, ABA plays a central signalling role during seed filling, interacting with master regulator genes such as ABI3 and FUS3, in a gene activation manner [reviewed in [65]]. Interestingly, FUS3 is one of the targets of both the AtCLF and AtMEA genes (acting in vegetative and reproductive stages, respectively) and it is silenced in leaves and closed flowers [30] where it was also shown to contain the repressive mark H3K27me3. In this work we examined the response of PcG genes to ABA after exogenous ABA application on seedlings and observed that both HvE(Z) and HvFIE genes are induced by ABA. The observed increase in HvE(Z) and HvFIE expression upon ABA treatment suggests that these genes might play a role as epigenetic regulators of ABA-mediated processes in seedlings. Chromatin modulators, such as histone deacetylase genes, have been shown previously to be affected by exogenous ABA in Arabidopsis, rice and barley [35,66,39]. This is the first time that an induction of PcG genes upon external ABA exposure has been demonstrated. It is possible that the expression of PcG genes is also affected by ABA during seed development, to activate or suppress key regulators, as the cell would require.

Conclusions

In this work we have presented the identification and characterization of four barley PcG genes, HvFIE, HvE(Z), HvSu(z)12a, and HvSu(z)12b. All genes were mapped on different barley chromosomes and co-localized with known chromosomal regions responsible for malting quality related traits. Should this be confirmed PcG genes might be used as molecular markers for marker-assisted selection in breeding programmes. Differential expression of HvFIE, HvE(Z), and HvSu(z)12b in different seed developmental stages and in two barley cultivars differing in seed size, suggested a role for these PcG genes in seed development. In addition HvFIE and HvE(Z) were found to be induced by the hormone ABA involved in seed development and stress response. The present work provides a basis for future studies aiming at unraveling the function of barley PcG genes and understanding seed development and stress-response epigenetic regulation in barley and other cereals.

Authors' contributions

AK conceived and designed the experiments, performed the quantitative real time PCR experiments, and wrote the manuscript. DP performed phylogenetic analysis and part of real time PCR experiments and participated in revising the manuscript. AT and EF performed the mapping experiments and participated in the writing of the manuscript. HA performed tissue sampling and qualitative RT-PCR experiments. KB supervised and attended all barley cultivations. MAS designed the mapping experiments and participated in revising the manuscript. AST conceived and directed the whole study, and participated in the writing and revising of the manuscript. All authors read and approved the final manuscript.

Contributor Information

Aliki Kapazoglou, Email: alikik@certh.gr.

Alessandro Tondelli, Email: a.tondelli@libero.it.

Dimitra Papaefthimiou, Email: dimitra.papaefthimiou@gmail.com.

Helen Ampatzidou, Email: eleniampatzidou@tellas.gr.

Enrico Francia, Email: enrico.francia@unimore.it.

Michele A Stanca, Email: michele@stanca.it.

Konstantinos Bladenopoulos, Email: kbladen@otenet.gr.

Athanasios S Tsaftaris, Email: tsaft@certh.gr.

Acknowledgements

This work was supported by a PENED grant (O3EΔ402/2003). Continuous support for the Institute of Agrobiotechnology/CERTH from the General Secretariat of Research and Technology of Greece is also acknowledged. We would also like to thank the three anonymous reviewers for critically improving the manuscript.

References

  1. Goldberg AD, Allis CD, Bernstein E. Epigenetics: a landscape takes shape. Cell. 2007;128:635–38. doi: 10.1016/j.cell.2007.02.006. [DOI] [PubMed] [Google Scholar]
  2. Wu JI, Lessard J, Crabtree GR. Understanding the words of chromatin regulation. Cell. 2009;136:200–206. doi: 10.1016/j.cell.2009.01.009. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Chen ZJ, Tian L. Roles of dynamic and reversible histone acetylation in plant development and polyploidy. Biochim Biophys Acta. 2007;1769:295–307. doi: 10.1016/j.bbaexp.2007.04.007. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Chinnusamy V, Gong Z, Zhu JK. Abscisic acid-mediated epigenetic processes in plant development and stress responses. J Integr Plant Biol. 2008;50:1187–1195. doi: 10.1111/j.1744-7909.2008.00727.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Chinnusamy V, Zhu JK. Epigenetic regulation of stress responses in plants. Curr Opin Plant Biol. 2009;12:133–139. doi: 10.1016/j.pbi.2008.12.006. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Olsen OA. Nuclear endosperm development in cereals and Arabidopsis thaliana. Plant Cell. 2004;16:S214–S227. doi: 10.1105/tpc.017111. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Gehring M, Choi Y, Fischer RL. Imprinting and seed development. Plant Cell. 2004. pp. S203–13. [DOI] [PMC free article] [PubMed]
  8. Huh JH, Bauer MJ, Hsieh TF, Fischer RL. Cellular Programming of Plant Gene Imprinting. Cell. 2008;132:735–744. doi: 10.1016/j.cell.2008.02.018. [DOI] [PubMed] [Google Scholar]
  9. Guitton AE, Page DR, Chambrier P, Lionnet C, Faure JE, Grossniklaus U, Berger F. Identification of new members of Fertilisation Independent Seed Polycomb Group pathway involved in the control of seed development in Arabidopsis thaliana. Development. 2004;131:2971–2981. doi: 10.1242/dev.01168. [DOI] [PubMed] [Google Scholar]
  10. Köhler C, Hennig L, Bouveret R, Gheyselinck J, Grossniklaus U, Gruissem W. Arabidopsis MSI1 is a component of the E(Z)/FIE Polycomb group complex and required for seed development. EMBO J. 2003;22:4804–4814. doi: 10.1093/emboj/cdg444. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Adams S, Vinkenoog R, Spielman M, Dickinson HG, Scott RJ. Parent-of-origin effects on seed development in Arabidopsis thaliana require DNA methylation. Development. 2000;127:2493–2502. doi: 10.1242/dev.127.11.2493. [DOI] [PubMed] [Google Scholar]
  12. Kinoshita T, Yadegari R, Harada JJ, Goldberg RB, Fischer RL. Imprinting of the MEDEA Polycomb gene in the Arabidopsis endosperm. Plant Cell. 1999;11:1945–1952. doi: 10.1105/tpc.11.10.1945. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Luo M, Bilodeu P, Dennis ES, Peacock JW, Chaudhury AML. Expression and parent-of-origin effects for FIS2, E(Z), and FIE in the endosperm and embryo of developing Arabidopsis seeds. Proc Natl Acad Sci USA. 2000;97:10637–10642. doi: 10.1073/pnas.170292997. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Yadegari R, Kinoshita T, Lotan O, Cohen G, Katz A, Choi Y, Katz A, Nakashima K, Harada JJ, Goldberg RB, Fischer RL, Ohad N. Mutations in the FIE and E(Z) Genes That Encode Interacting Polycomb Proteins Cause Parent-of-Origin Effects on Seed Development by Distinct Mechanisms. Plant Cell. 2000;12:2367–2382. doi: 10.1105/tpc.12.12.2367. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Chanvivattana Y, Bishopp A, Schubert D, Stock C, Moon Y-H, Sung ZR, Goodrich J. Interaction of Polycomb-group proteins controlling flowering in Arabidopsis. Development. 2004;131:5263–5276. doi: 10.1242/dev.01400. [DOI] [PubMed] [Google Scholar]
  16. Cao R, Zhang Y. The functions of E(Z)/EZH2-mediated methylation of lysine 27 in histone H3. Curr Opin Genet Dev. 2004;14:155–164. doi: 10.1016/j.gde.2004.02.001. [DOI] [PubMed] [Google Scholar]
  17. Köhler C, Villar CBR. Programming of gene expression by Polycomb group proteins. Trends Cell Biol. 2008;18:236–243. doi: 10.1016/j.tcb.2008.02.005. [DOI] [PubMed] [Google Scholar]
  18. Schatlowski N, Creasy K, Goodrich J, Schubert D. Keeping plants in shape: Polycomb-group genes and histone methylation. Sem Cell Dev Biol. 2008;19:547–553. doi: 10.1016/j.semcdb.2008.07.019. [DOI] [PubMed] [Google Scholar]
  19. Grossniklaus U, Vielle-Cazalda JP, Hoepner MA, Gagliano W. Maternal Control of Embryogenesis by MEDEA, a Polycomb Group Gene in Arabidopsis thaliana. Science. 1998;280:448–449. doi: 10.1126/science.280.5362.446. [DOI] [PubMed] [Google Scholar]
  20. Ohad N, Yadegari R, Margossian L, Hannon M, Michaeli D, Harada JJ, Goldberg RB, Fischer RL. Mutations in FIE, a WD Polycomb group gene, allow endosperm development without fertilization. Plant Cell. 1999;11:407–416. doi: 10.1105/tpc.11.3.407. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Schubert D, Primavesi L, Bishopp A, Roberts G, Doonan J, Jenuwein T, Goodrich J. Silencing by plant Polycomb-group genes requires dispersed trimethylation of histone H3 at lysine 27. EMBO J. 2006;25:4638–4649. doi: 10.1038/sj.emboj.7601311. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Sung S, Amasino RM. Vernalization in Arabidopsis thaliana is mediated by the PhD finger protein VIN3. Nature. 2004;427:159–164. doi: 10.1038/nature02195. [DOI] [PubMed] [Google Scholar]
  23. Wood CC, Robertson M, Tanner G, Peacock WJ, Dennis ES, Helliwell CA. The Arabidopsis thaliana vernalization response requires a polycomb-like protein complex that also includes VERNALIZATION INSENSITIVE 3. Proc Natl Acad Sci USA. 2006;103:14631–14636. doi: 10.1073/pnas.0606385103. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Birve A, Sengupta AK, Beuchle D, Larsson J, Kennison JA, Rasmuson-Lestander A, Müller J. Su(z)12, a novel Drosophila Polycomb group gene that is conserved in vertebrates and plants. Development. 2001;128:3371–3379. doi: 10.1242/dev.128.17.3371. [DOI] [PubMed] [Google Scholar]
  25. Köhler C, Hennig L, Spillane C, Pien S, Gruissem W, Grossniklaus U. The Polycomb-group protein MEDEA regulates seed development by controlling expression of the MADS-box gene PHERES1. Genes Dev. 2003;17:1540–1553. doi: 10.1101/gad.257403. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Köhler C, Hennig L, Page D, Gagliardini V, Gruissem W, Grossniklaus U. The Arabidopsis thaliana MEDEA Polycomb group protein controls expression of PHERES 1 by parental imprinting. Nature Genet. 2004;37:28–30. doi: 10.1038/ng1495. [DOI] [PubMed] [Google Scholar]
  27. Makarevich G, Villar CBR, Erilova A, Köhler C. Mechanism of PHERES1 imprinting in Arabidopsis. J Cell Science. 2008;121:906–912. doi: 10.1242/jcs.023077. [DOI] [PubMed] [Google Scholar]
  28. Gehring M, Huh JH, Hsieh TF, Penterman J, Choi Y, Harada JJ, Goldberg RB, Fischer RL. DEMETER DNA glycosylase establishes MEDEA polycomb gene self-imprinting by allele-specific demethylation. Cell. 2006;124:495–506. doi: 10.1016/j.cell.2005.12.034. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Jullien PE, Katz A, Oliva M, Ohad N, Berger F. Polycomb Group complexes self-regulate imprinting of the Polycomb Group gene MEDEA in Arabidopsis. Curr Biol. 2006;16:486–492. doi: 10.1016/j.cub.2006.01.020. [DOI] [PubMed] [Google Scholar]
  30. Makarevich G, Leroy O, Akinci U, Schubert D, Clarenz O, Goodrich J, Grossniklaus U, Köhler C. Different. Polycomb group complexes regulate common target genes in Arabidopsis. EMBO Rep. 2006;7:947–952. doi: 10.1038/sj.embor.7400760. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Finkelstein RR, Gampala SS, Rock CD. Abscisic acid signalling in seeds and seedlings. Plant Cell. 2002;14:S15–S45. doi: 10.1105/tpc.010441. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Nambara E, Marion-Poll A. Abscisic acid biosynthesis and catabolism. Annu Rev Plant Biol. 2005;56:165–185. doi: 10.1146/annurev.arplant.56.032604.144046. [DOI] [PubMed] [Google Scholar]
  33. Ng DWK, Chandrasekharan MB, Hall TC. Ordered histone modifications are associated with transcriptional poising and activation of the phaseolin promoter. Plant Cell. 2006;18:119–132. doi: 10.1105/tpc.105.037010. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Perruc E, Kinoshita N, Lopez-Molina L. The role of chromatin-remodeling factor PKL in balancing osmotic stress responses during Arabidopsis seed germination. Plant J. 2007;52:927–936. doi: 10.1111/j.1365-313X.2007.03288.x. [DOI] [PubMed] [Google Scholar]
  35. Sridha S, Wu K. Identification of AtHD2C as a novel regulator of abscisic acid responses in Arabidopsis. Plant J. 2006;46:124–133. doi: 10.1111/j.1365-313X.2006.02678.x. [DOI] [PubMed] [Google Scholar]
  36. Saez A, Rodrigues A, Santiago J, Rubio S, Rodriguez PL. HAB1-SWI3B interaction reveals a link between abscisic acid signaling and putative SWI/SNF chromatin-remodeling complexes in Arabidopsis. Plant Cell. 2008;20:2972–88. doi: 10.1105/tpc.107.056705. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Yin H, Zhang X, Liu J, Wang Y, He J, Yang T, Hong X, Yang Q, Gong Z. Epigenetic regulation, somatic homologous recombination, and abscisic acid signaling are influenced by DNA polymerase epsilon mutation in Arabidopsis. Plant Cell. 2009;21:386–402. doi: 10.1105/tpc.108.061549. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Sreenivasulu N, Usadel B, Winter A, Radchuk V, Scholz U, Stein N, Weschke W, Strickert M, Close TJ, Stittt M, Graner A, Wobus U. Barley grain maturation and germination: metabolic pathway and regulatory network commonalities and differences highlighted by new MapMan/PageMan profiling tools. Plant Phys. 2008;146:1738–1758. doi: 10.1104/pp.107.111781. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Demetriou K, Kapazolgou A, Tondelli A, Francia E, Stanca MS, Bladenopoulos K, Tsaftaris AS. Epigenetic chromatin modifiers in barley: I. Cloning, mapping and expression analysis of the plant specific HD2 family of histone deacetylases from barley, during seed development and after hormonal treatment. Physiol Plant. 2009;136:358–368. doi: 10.1111/j.1399-3054.2009.01236.x. [DOI] [PubMed] [Google Scholar]
  40. Demetriou K, Kapazolgou A, Bladenopoulos K, Tsaftaris AS. Epigenetic chromatin modifiers in barley: II. Characterization and expression analysis of the HDA1 family of barley histone deacetylases during development and in response to jasmonic acid. Plant Mol Biol Rep. 2010;28:9–21. doi: 10.1007/s11105-009-0121-4. [DOI] [Google Scholar]
  41. Papaefthimiou D, Likotrafiti E, Kapazoglou A, Bladenopoulos K, Tsaftaris A. Epigenetic chromatin modifiers in barley: III. Isolation and characterization of the barley GNAT-MYST family of histone acetyltransferases and responses to exogenous ABA. Plant Physiol Biochem. 2010;48:98–107. doi: 10.1016/j.plaphy.2010.01.002. [DOI] [PubMed] [Google Scholar]
  42. Altschul SF, Gish W, Miller W, Myers EW, Lippman DJ. Basic Local Alignment Search Tool. J Mol Biol. 1993;215:403–410. doi: 10.1016/S0022-2836(05)80360-2. [DOI] [PubMed] [Google Scholar]
  43. Thomson JD, Higgins DG, Gibson TJ. ClustalW: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucl Acids Res. 1994;22:4673–80. doi: 10.1093/nar/22.22.4673. [DOI] [PMC free article] [PubMed] [Google Scholar]
  44. Kumar S, Tamura K, Nei M. MEGA3: Integrated software for Molecular Evolutionary Genetics Analysis and sequence alignment. Briefings in Bioinformatics. 2004;5:150–63. doi: 10.1093/bib/5.2.150. [DOI] [PubMed] [Google Scholar]
  45. Saitou N, Nei M. The neighbor-joining method: a new method for reconstructing phylogenetic trees. Mol Biol. 1987;E 4:406–25. doi: 10.1093/oxfordjournals.molbev.a040454. [DOI] [PubMed] [Google Scholar]
  46. Ronquist F, Huelsenbeck JP. MRBAYES 3: Bayesian phylogenetic inference under mixed models. Bioinformatics. 2003;19:1572–1574. doi: 10.1093/bioinformatics/btg180. [DOI] [PubMed] [Google Scholar]
  47. Page RDM. TreeView: An application to display phylogenetic trees on personal computers. Computer Applications in the Biosciences. 1996;12:357–358. doi: 10.1093/bioinformatics/12.4.357. [DOI] [PubMed] [Google Scholar]
  48. Costa MJ, Corey A, Hayes PM, Jobet C, Kleinhofs A, Kopisch-Obusch A, Kramer SF, Kudrna D, Li M, Riera-Lizarazu O, Sato K, Szucs P, Toojinda T, Vales MI, Wolfe RI. Molecular mapping of the Oregon Wolfe Barleys: a phenotypically polymorphic doubled-haploid population. Theor Appl Genet. 2001;103:415–24. doi: 10.1007/s001220100622. [DOI] [Google Scholar]
  49. Marcel TC, Varshney RK, Barbieri M, Jafary H, de Kock MJD, Graner A, Niks RE. A high-density consensus map of barley to compare the distribution of QTLs of partial resistance to Puccinia hordei and of defense gene homologues. Theor Appl Genet. 2007;114:487–500. doi: 10.1007/s00122-006-0448-2. [DOI] [PubMed] [Google Scholar]
  50. Rozen S, Skaletsky H. Primer3 on the WWW for general users and for biologist programmers. Meth Mol Biol. 2000;132:365–86. doi: 10.1385/1-59259-192-2:365. [DOI] [PubMed] [Google Scholar]
  51. Neff MM, Neff JD, Chory J, Pepper AE. dCAPS, a simple technique for genetic analysis of single nucleotide polymorphisms: experimental applications in Arabidopsis thaliana genetics. Plant J. 1998;14:387–392. doi: 10.1046/j.1365-313X.1998.00124.x. [DOI] [PubMed] [Google Scholar]
  52. Van Ooijen JW. Joinmap®: Software for the calculation of genetic linkage maps in experimental populations Version 4. Wageningen (The Netherlands): Kyazma BV; 2006. [Google Scholar]
  53. Szűcs P, Blake VC, Bhat PR, Chao S, Close TJ, Cuesta-Marcos A, Muehlbauer GJ, Ramsay L, Waugh R, Hayes PM. An Integrated Resource for Barley Linkage Map and Malting Quality QTL Alignment. Plant Genome. 2008;2:134–140. doi: 10.3835/plantgenome2008.01.0005. [DOI] [Google Scholar]
  54. Pfaffl MW, Horgan GW, Dempfle L. Relative expression software tool (REST) for group-wise comparison and statistical analysis of relative expression results in real-time PCR. Nucleic Acids Res. 2002;30:e36. doi: 10.1093/nar/30.9.e36. [DOI] [PMC free article] [PubMed] [Google Scholar]
  55. Shen Q, Chen CN, Brands A, Pan SM, Ho TH. The stress- and abscisic acid-induced barley gene HVA22: developmental regulation and homologues in diverse organisms. Plant Mol. 2001;45:327–340. doi: 10.1023/A:1006460231978. [DOI] [PubMed] [Google Scholar]
  56. Wang D, Tyson MD, Jackson SS, Yadegari R. Partially redundant functions of two SET-domain polycomb-group proteins in controlling initiation of seed development in Arabidopsis. Proc Natl Acad Sci. 2006;103:13244–13249. doi: 10.1073/pnas.0605551103. [DOI] [PMC free article] [PubMed] [Google Scholar]
  57. Spillane C, Schmid KJ, Laoueille-Duprat S, Pien S, Escobar-Restrepo JM, Baroux C, Gagliardini V, Page DR, Wolfe KH, Grossniklaus U. Positive darwinian selection at the imprinted MEDEA locus in plants. Nature. 2007;448:349–352. doi: 10.1038/nature05984. [DOI] [PubMed] [Google Scholar]
  58. Springer NM, Danilevskaya ON, Hermon P, Helentjaris TG, Phillips RL, Kaeppler HF, Kaeppler SM. Sequence relationships, conserved domains and expression patterns for maize homologs of the polycomb group genes E(z), esc and E(Pc) Plant Physiol. 2002;128:1332–1345. doi: 10.1104/pp.010742. [DOI] [PMC free article] [PubMed] [Google Scholar]
  59. Thakur J, Malik MP, Bhatt V, Reddy M, Sopory S, Tyagi AK, Khurana J. A POLYCOMB group gene of rice (Oryza sativa L subspecies indica) OsiEZ1, codes for a nuclear-localized protein expressed preferentially in young shoots and during reproductive development. Gene. 2003;313:1–13. doi: 10.1016/S0378-1119(03)00723-6. [DOI] [PubMed] [Google Scholar]
  60. Luo M, Platten D, Chaudhury A, Peacock WJ, Dennis ES. Expression, imprinting, and evolution of rice homologues of the Polycomb group genes. Molecular Plant. 2009;2:711–723. doi: 10.1093/mp/ssp036. [DOI] [PubMed] [Google Scholar]
  61. Fox GP, Panozzo JF, Li CD, Lance RCM, Henry RJ. Molecular basis of barley quality. Aust J. 2003;54:1081–1101. [Google Scholar]
  62. Spillane C, MacDougall C, Stock C, Köhler C, Vielle-Gazalda JP, Nunes SM, Grossniklaus U, Goodrich J. Interaction of the Arabidopsis Polycomb group proteins FIE and E(Z) mediates their common phenotypes. Curr Biol. 2000;10:1535–1538. doi: 10.1016/S0960-9822(00)00839-3. [DOI] [PubMed] [Google Scholar]
  63. Danilevskaya ON, Hermon P, Hantke S, Muszynski MG, Kollipara K, Ananiev EV. Duplicated FIE genes in maize: expression pattern and imprinting suggest distinct functions. Plant Cell. 2003;15:425–438. doi: 10.1105/tpc.006759. [DOI] [PMC free article] [PubMed] [Google Scholar]
  64. Kiyosue T, Ohad N, Yadegari R, Hannon M, Dinneny J, Wells D, Katz A, Margossian L, Harada JJ, Goldberg RB, Fisher RL. Control of fertilization independent endosperm development by the MEDEA polycomb gene in Arabidopsis. Proc Natl Acad Sci USA. 1999;96:4186–4191. doi: 10.1073/pnas.96.7.4186. [DOI] [PMC free article] [PubMed] [Google Scholar]
  65. Verdier J, Thompson RD. Transcriptional regulation of storage protein synthesis during dicotyledon seed filling. Plant Cell Physiol. 2008;49:1263–71. doi: 10.1093/pcp/pcn116. [DOI] [PubMed] [Google Scholar]
  66. Fu W, Wu K, Duan J. Sequence and expression analysis of histone deacetylases in rice. Biochem Biophys Res Comm. 2007;356:843–850. doi: 10.1016/j.bbrc.2007.03.010. [DOI] [PubMed] [Google Scholar]

Articles from BMC Plant Biology are provided here courtesy of BMC

RESOURCES