Skip to main content
Nucleic Acids Research logoLink to Nucleic Acids Research
. 1998 Feb 15;26(4):1056–1062. doi: 10.1093/nar/26.4.1056

A contiguous 60 kb genomic stretch from barley reveals molecular evidence for gene islands in a monocot genome.

R Panstruga 1, R Büschges 1, P Piffanelli 1, P Schulze-Lefert 1
PMCID: PMC147355  PMID: 9461468

Abstract

The contiguous DNA sequence of a 60 kb genomic interval of barley chromosome 4HL has been assembled. The region harbours a single and novel gypsy -like retrotransposon, designated BAGY-1. Only three genes appear to reside in the genomic stretch. One predicts a plant homologue of ribophorin I, a subunit of the oligosaccharyltransferase-protein complex located in the rough endoplasmatic reticulum. The second is similar to the Drosophila g1 gene encoding a ring finger protein involved in developmental processes. The observed gene density is approximately 5-fold lower than in the best characterized dicot genome of Arabidopsis but 6- to 10-fold higher than expected from an equidistant gene distribution in the complex barley genome. Our data suggest that the 60 kb genomic interval represents part of a gene island, a seemingly distinctive feature of grass genomes.

Full Text

The Full Text of this article is available as a PDF (323.6 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Antequera F., Bird A. P. Unmethylated CpG islands associated with genes in higher plant DNA. EMBO J. 1988 Aug;7(8):2295–2299. doi: 10.1002/j.1460-2075.1988.tb03072.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Barakat A., Carels N., Bernardi G. The distribution of genes in the genomes of Gramineae. Proc Natl Acad Sci U S A. 1997 Jun 24;94(13):6857–6861. doi: 10.1073/pnas.94.13.6857. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bennetzen J. L. The contributions of retroelements to plant genome organization, function and evolution. Trends Microbiol. 1996 Sep;4(9):347–353. doi: 10.1016/0966-842x(96)10042-1. [DOI] [PubMed] [Google Scholar]
  4. Bernardi G. The human genome: organization and evolutionary history. Annu Rev Genet. 1995;29:445–476. doi: 10.1146/annurev.ge.29.120195.002305. [DOI] [PubMed] [Google Scholar]
  5. Bouchard M. L., Côté S. The Drosophila melanogaster developmental gene g1 encodes a variant zinc-finger-motif protein. Gene. 1993 Mar 30;125(2):205–209. doi: 10.1016/0378-1119(93)90330-6. [DOI] [PubMed] [Google Scholar]
  6. Büschges R., Hollricher K., Panstruga R., Simons G., Wolter M., Frijters A., van Daelen R., van der Lee T., Diergaarde P., Groenendijk J. The barley Mlo gene: a novel control element of plant pathogen resistance. Cell. 1997 Mar 7;88(5):695–705. doi: 10.1016/s0092-8674(00)81912-1. [DOI] [PubMed] [Google Scholar]
  7. Carels N., Barakat A., Bernardi G. The gene distribution of the maize genome. Proc Natl Acad Sci U S A. 1995 Nov 21;92(24):11057–11060. doi: 10.1073/pnas.92.24.11057. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Crimaudo C., Hortsch M., Gausepohl H., Meyer D. I. Human ribophorins I and II: the primary structure and membrane topology of two highly conserved rough endoplasmic reticulum-specific glycoproteins. EMBO J. 1987 Jan;6(1):75–82. doi: 10.1002/j.1460-2075.1987.tb04721.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Cross S. H., Bird A. P. CpG islands and genes. Curr Opin Genet Dev. 1995 Jun;5(3):309–314. doi: 10.1016/0959-437x(95)80044-1. [DOI] [PubMed] [Google Scholar]
  10. Fickett J. W. Finding genes by computer: the state of the art. Trends Genet. 1996 Aug;12(8):316–320. doi: 10.1016/0168-9525(96)10038-x. [DOI] [PubMed] [Google Scholar]
  11. Grandbastien M. A. Retroelements in higher plants. Trends Genet. 1992 Mar;8(3):103–108. doi: 10.1016/0168-9525(92)90198-d. [DOI] [PubMed] [Google Scholar]
  12. Harnik-Ort V., Prakash K., Marcantonio E., Colman D. R., Rosenfeld M. G., Adesnik M., Sabatini D. D., Kreibich G. Isolation and characterization of cDNA clones for rat ribophorin I: complete coding sequence and in vitro synthesis and insertion of the encoded product into endoplasmic reticulum membranes. J Cell Biol. 1987 Apr;104(4):855–863. doi: 10.1083/jcb.104.4.855. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Kelleher D. J., Kreibich G., Gilmore R. Oligosaccharyltransferase activity is associated with a protein complex composed of ribophorins I and II and a 48 kd protein. Cell. 1992 Apr 3;69(1):55–65. doi: 10.1016/0092-8674(92)90118-v. [DOI] [PubMed] [Google Scholar]
  14. Knoop V., Unseld M., Marienfeld J., Brandt P., Sünkel S., Ullrich H., Brennicke A. copia-, gypsy- and LINE-like retrotransposon fragments in the mitochondrial genome of Arabidopsis thaliana. Genetics. 1996 Feb;142(2):579–585. doi: 10.1093/genetics/142.2.579. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Langdale J. A., Taylor W. C., Nelson T. Cell-specific accumulation of maize phosphoenolpyruvate carboxylase is correlated with demethylation at a specific site greater than 3 kb upstream of the gene. Mol Gen Genet. 1991 Jan;225(1):49–55. doi: 10.1007/BF00282641. [DOI] [PubMed] [Google Scholar]
  16. Larsen F., Gundersen G., Lopez R., Prydz H. CpG islands as gene markers in the human genome. Genomics. 1992 Aug;13(4):1095–1107. doi: 10.1016/0888-7543(92)90024-m. [DOI] [PubMed] [Google Scholar]
  17. Le Guen L., Thomas M., Kreis M. Gene density and organization in a small region of the Arabidopsis thaliana genome. Mol Gen Genet. 1994 Nov 1;245(3):390–396. doi: 10.1007/BF00290120. [DOI] [PubMed] [Google Scholar]
  18. Manninen I., Schulman A. H. BARE-1, a copia-like retroelement in barley (Hordeum vulgare L.). Plant Mol Biol. 1993 Aug;22(5):829–846. doi: 10.1007/BF00027369. [DOI] [PubMed] [Google Scholar]
  19. Miklos G. L., Rubin G. M. The role of the genome project in determining gene function: insights from model organisms. Cell. 1996 Aug 23;86(4):521–529. doi: 10.1016/s0092-8674(00)80126-9. [DOI] [PubMed] [Google Scholar]
  20. Montero L. M., Salinas J., Matassi G., Bernardi G. Gene distribution and isochore organization in the nuclear genome of plants. Nucleic Acids Res. 1990 Apr 11;18(7):1859–1867. doi: 10.1093/nar/18.7.1859. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Moore G., Devos K. M., Wang Z., Gale M. D. Cereal genome evolution. Grasses, line up and form a circle. Curr Biol. 1995 Jul 1;5(7):737–739. doi: 10.1016/s0960-9822(95)00148-5. [DOI] [PubMed] [Google Scholar]
  22. Purugganan M. D., Wessler S. R. Molecular evolution of magellan, a maize Ty3/gypsy-like retrotransposon. Proc Natl Acad Sci U S A. 1994 Nov 22;91(24):11674–11678. doi: 10.1073/pnas.91.24.11674. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Quigley F., Dao P., Cottet A., Mache R. Sequence analysis of an 81 kb contig from Arabidopsis thaliana chromosome III. Nucleic Acids Res. 1996 Nov 1;24(21):4313–4318. doi: 10.1093/nar/24.21.4313. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. SWARTZ M. N., TRAUTNER T. A., KORNBERG A. Enzymatic synthesis of deoxyribonucleic acid. XI. Further studies on nearest neighbor base sequences in deoxyribonucleic acids. J Biol Chem. 1962 Jun;237:1961–1967. [PubMed] [Google Scholar]
  25. SanMiguel P., Tikhonov A., Jin Y. K., Motchoulskaia N., Zakharov D., Melake-Berhan A., Springer P. S., Edwards K. J., Lee M., Avramova Z. Nested retrotransposons in the intergenic regions of the maize genome. Science. 1996 Nov 1;274(5288):765–768. doi: 10.1126/science.274.5288.765. [DOI] [PubMed] [Google Scholar]
  26. Silberstein S., Collins P. G., Kelleher D. J., Rapiejko P. J., Gilmore R. The alpha subunit of the Saccharomyces cerevisiae oligosaccharyltransferase complex is essential for vegetative growth of yeast and is homologous to mammalian ribophorin I. J Cell Biol. 1995 Feb;128(4):525–536. doi: 10.1083/jcb.128.4.525. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Smyth D. R., Kalitsis P., Joseph J. L., Sentry J. W. Plant retrotransposon from Lilium henryi is related to Ty3 of yeast and the gypsy group of Drosophila. Proc Natl Acad Sci U S A. 1989 Jul;86(13):5015–5019. doi: 10.1073/pnas.86.13.5015. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Sørensen M. B., Müller M., Skerritt J., Simpson D. Hordein promoter methylation and transcriptional activity in wild-type and mutant barley endosperm. Mol Gen Genet. 1996 Apr 10;250(6):750–760. doi: 10.1007/BF02172987. [DOI] [PubMed] [Google Scholar]
  29. Tremousaygue D., Bardet C., Dabos P., Regad F., Pelese F., Nazer R., Gander E., Lescure B. Genome DNA sequencing around the EF-1 alpha multigene locus of Arabidopsis thaliana indicates a high gene density and a shuffling of noncoding regions. Genome Res. 1997 Mar;7(3):198–209. doi: 10.1101/gr.7.3.198. [DOI] [PubMed] [Google Scholar]

Articles from Nucleic Acids Research are provided here courtesy of Oxford University Press

RESOURCES