Table 1.
Functional Profiling of phy-Regulated Early-Response Genes for Photomorphogenic Phenotypes
| (Class) Numbers | Arabidopsis Genome Initiative Number | Protein Name Designation | Functional Category | T-DNA Line (in This Study) | Mutant Line Designation | Insertion/Transcript | Hypocotyl Length
|
Cotyledon Area (Rc) | Reported Function for This Locus | |
|---|---|---|---|---|---|---|---|---|---|---|
| FRc | Rc | |||||||||
| (I) Aberrant photomorphogenic phenotype displayed | ||||||||||
| 1 | At2g46790AI | APRR9 | Transcription | prr9-11 | null1 | None | Tall | Small | Circadian rhythms | |
| 2 | At2g46970AR | PIL1 | Transcription | SALK_025372 | pil1-2 | Null^ | Tall | Tall | Small | |
| pil1-12 | Null2 | Hyposensitive in R, FR, and Low R/FR | Shade avoidance2 | |||||||
| 3 | At5g11260AI | HY5 | Transcription | SAIL_19_G04 | hy5-101 | S+26^ | Tall | Tall | Small | |
| hy5-13,4 | Null3,4 | Hyposensitive in R, FR, B, WL | Transcription | |||||||
| 4 | At2g02950AI | PKS1 | Signaling | SAIL_828_H11 | pks1-101 | −552^ | Short | Short | Large | |
| pks15 | Null5 | phyA VLFR in FRp | phyA signaling5 | |||||||
| 5 | At2g46340AI | SPA1 | Signaling | spa1-3RLD,6,7 | Null6,7 | Short | Short | Large | Suppressor of phyA6,7 | |
| 6 | At2g37970AI | SOUL family | Unknown | SAIL_1280_E03 | soul1 | −35^ | None | Short | Large | ND |
| 7 | At2g40080AI | ELF4 | Signaling | SAIL_1244_G01 | elf4-1018 | Null8 | None | Tall | Small | phyB signaling8 |
| (II) Parallel, unidirectional defect in both hypocotyl and cotyledon photoresponsiveness displayed | ||||||||||
| 8 | At3g10910AI | RING-ZFN | Transcription | SAIL_256_C02 | 418^ | None | Short | Small | ND | |
| 9 | At3g21150AI | B-box type ZF | Transcription | SALK_059534 | 670^ | None | Short | Small | ND | |
| 10 | At5g24120AI | SIGE | Transcription | SALK_141383 | 383^ | Short | Short | Small | ND | |
| 11 | At5g37260AI | CCA1-L | Transcription | SALK_074896 | 1192^ | Tall | Tall | Large | ND | |
| 12 | At1g78820AI | Putative EP1 | Signaling | SAIL_639_F10 | 1110^ | Short | Short | Small | ND | |
| 13 | At2g20750AR | β-Expansin | Growth | SAIL_345_G11 | 519^ | None | Short | Small | Loosen cell wall | |
| 14 | At1g61890AI | MATE | Unknown | SAIL_749_F06 | −211^ | Short | Short | Small | ND | |
| (III) Aberrant photoresponsive phenotype in hypocotyl only displayed | ||||||||||
| 15 | At1g01060AI | LHY | Transcription | lhy-101 | Null | Short | Short | None | ||
| lhy-11, -12, -13le,9 | LoF9 | Same as wild-type in LD conditions | Circadian rhythms | |||||||
| 16 | At2g31380AI | STH (ZF3) | Transcription | SAIL_786_F08 | −442^ | Short | Short | None | ND | |
| 17 | At3g47500ABI | Dof-type ZF | Transcription | SAIL_434_G09 | 651^ | None | Short | None | ND | |
| 18 | At4g25480AI,BI | CBF3 | Transcription | SAIL_244_D02 | 48^ | None | Short | None | Cold tolerance10 | |
| 19 | At2g42870AR | Expressed | Unknown | SAIL_668_E10 | S+10^ | Short | Short | None | ND | |
| 20 | At4g14690AI | ELIP1 | Unknown | SAIL_667_C04 | 1316^ | Short | Short | None | Photoprotection11 | |
| (IV) No aberrant seedling phenotype displayed | ||||||||||
| 21 | At1g18330AI | EPR112 | Transcription | SAIL_195_F11 | 602^ | None | None | None | Slave oscillator12 | |
| 22 | At2g44910AR | ATHB413 | Transcription | SALK_104843 | 1365^ | None | None | None | Shade avoidance13 | |
| 23 | At2g46830AI | CCA1 | Transcription | cca1-1w,14 | Null14 | None | None | None | Circadian rhythms14 | |
| 24 | At3g02380AI | COL215 | Transcription | SAIL_70_F03 | −258^ | None | None | None | Circadian-regulated15 | |
| 25 | At3g21330AR | bHLH08716 | Transcription | SALK_066339 | 487^ | None | None | None | ND | |
| 26 | At4g16780AR | HAT417 | Transcription | SALK_106790 | 162^ | None | None | None | Development17 | |
| 27 | At5g44260AR | Putative ZF | Transcription | SAIL_1277_D05 | 360^ | None | None | None | ND | |
| 28 | At1g78070AI | WD-40 protein | Signaling | SAIL_1264_G10 | −4^ | None | None | None | ND | |
| 29 | At2g30040AI | Putative PK | Signaling | SAIL_1175_F12 | 981^ | Short* | None | None | ND | |
| 30 | At4g26850AI | VTC2 | Unknown | SAIL_769_H05 | 620^ | None | None | None | ND | |
| 31 | At4g27520AI | Plastocyanin-L | Unknown | SAIL_437_B03 | −206^ | None | None | None | ND | |
| 32 | At5g52250AI | COP1-L | Unknown | SALK_060638 | 298^ | None | None | None | ND | |
List of 32 genes analyzed, including Arabidopsis Genome Initiative loci and designated protein names. The corresponding mutant lines isolated in this work (SAIL or SALK lines) and previously identified mutant lines are indicated. The predicted T-DNA insertion sites within the respective genes, relative to the start codon, are shown. In some mutant lines, the T-DNA insertion sites were upstream of the start codon (−) or downstream of the stop codon (S+). Based on the statistical significance (see Supplemental Figures 3 and 4 online) of differences observed in hypocotyl length and cotyledon area between wild-type and mutant seedlings grown in Rc light, genes were grouped into four classes, as indicated. Functions previously reported for some of the genes are listed. One of the lines (line 29) displays a short-hypocotyl phenotype only in FRc light (asterisk). ^, transcript not detected in the mutant (see Supplemental Figures 2 and 5 online). AI, phyA early-induced genes; AR, phyA early-repressed genes; BI, phyB early-induced gene; ABI, phyA/B early-induced gene; R, red light; FR, far-red light; B, blue light; WL, white light; FRp, far-red pulse; VLFR, very-low-fluence response; LD, long day (16-h-light/8-h-dark cycles); Lof, loss of function; ND, not determined; le, Landsberg erecta (wild type); rld, RLD (wild type); w, Wassilewskija (wild type). References are designated as follows: 1, Eriksson et al. (2003); 2, Salter et al. (2003); 3, Koornneef et al. (1980); 4, Ang et al. (1998); 5, Lariguet et al. (2003); 6, Hoecker et al. (1998); 7, Hoecker et al. (1999); 8, Khanna et al. (2003); 9, Mizoguchi et al. (2002); 10, Gong et al. (2002); 11, Hutin et al. (2003); 12, Kuno et al. (2003); 13, Carabelli et al. (1993); 14, Green and Tobin (1999); 15, Ledger et al. (2001); 16, Bailey et al. (2003); 17, Schena et al. (1993).