Skip to main content
Genetics logoLink to Genetics
. 2001 Mar;157(3):1321–1330. doi: 10.1093/genetics/157.3.1321

Arabidopsis and Brassica comparative genomics: sequence, structure and gene content in the ABI-Rps2-Ck1 chromosomal segment and related regions.

C F Quiros 1, F Grellet 1, J Sadowski 1, T Suzuki 1, G Li 1, T Wroblewski 1
PMCID: PMC1461565  PMID: 11238417

Abstract

The region corresponding to the ABI1-Rps2-Ck1 segment on chromosome 4 of Arabidopsis thaliana was sequenced in Brassica oleracea. Similar to A. thaliana, the B. oleracea homolog BoRps2 is present in single copy. The B. oleracea orthologous segment was located on chromosome 4 and can be distinguished by the presence of an N-myristoyl transferase coding gene (N-myr) between the Rps2 and Ck1 (BoCk1a) genes. The N-myr homologs in Arabidopsis are on chromosomes 2 and 5. Additional homologs for Ck1 are located on these two chromosomes. A second Ck1 homolog found on B. oleracea (BoCk1b) chromosome 7 served to define another orthologous segment located in Arabidopsis chromosome 1. The two segments displayed identical gene content and order in both species, namely BoCK1b, a gene encoding a hypothetical protein (BohypothA) and transcription factor eiF4A. High levels of sequence identity were observed for the coding sequences of all genes examined. Although in general larger spacers were found in Brassica than in A. thaliana, this was not always the case. Promoters were poorly conserved, except for several sequence stretches of a few nucleotides. Comparative sequencing revealed microsyntenic changes resulting from chromosomal structural rearrangements, which are often undetectable by genetic mapping.

Full Text

The Full Text of this article is available as a PDF (243.8 KB).

Selected References

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

  1. Altschul S. F., Gish W., Miller W., Myers E. W., Lipman D. J. Basic local alignment search tool. J Mol Biol. 1990 Oct 5;215(3):403–410. doi: 10.1016/S0022-2836(05)80360-2. [DOI] [PubMed] [Google Scholar]
  2. Arabidopsis Genome Initiative Analysis of the genome sequence of the flowering plant Arabidopsis thaliana. Nature. 2000 Dec 14;408(6814):796–815. doi: 10.1038/35048692. [DOI] [PubMed] [Google Scholar]
  3. Blanc G., Barakat A., Guyot R., Cooke R., Delseny M. Extensive duplication and reshuffling in the Arabidopsis genome. Plant Cell. 2000 Jul;12(7):1093–1101. doi: 10.1105/tpc.12.7.1093. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Burge C. B., Karlin S. Finding the genes in genomic DNA. Curr Opin Struct Biol. 1998 Jun;8(3):346–354. doi: 10.1016/s0959-440x(98)80069-9. [DOI] [PubMed] [Google Scholar]
  5. Copenhaver G. P., Nickel K., Kuromori T., Benito M. I., Kaul S., Lin X., Bevan M., Murphy G., Harris B., Parnell L. D. Genetic definition and sequence analysis of Arabidopsis centromeres. Science. 1999 Dec 24;286(5449):2468–2474. doi: 10.1126/science.286.5449.2468. [DOI] [PubMed] [Google Scholar]
  6. Gale M. D., Devos K. M. Plant comparative genetics after 10 years. Science. 1998 Oct 23;282(5389):656–659. doi: 10.1126/science.282.5389.656. [DOI] [PubMed] [Google Scholar]
  7. Grant D., Cregan P., Shoemaker R. C. Genome organization in dicots: genome duplication in Arabidopsis and synteny between soybean and Arabidopsis. Proc Natl Acad Sci U S A. 2000 Apr 11;97(8):4168–4173. doi: 10.1073/pnas.070430597. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Hebsgaard S. M., Korning P. G., Tolstrup N., Engelbrecht J., Rouzé P., Brunak S. Splice site prediction in Arabidopsis thaliana pre-mRNA by combining local and global sequence information. Nucleic Acids Res. 1996 Sep 1;24(17):3439–3452. doi: 10.1093/nar/24.17.3439. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Higo K., Ugawa Y., Iwamoto M., Higo H. PLACE: a database of plant cis-acting regulatory DNA elements. Nucleic Acids Res. 1998 Jan 1;26(1):358–359. doi: 10.1093/nar/26.1.358. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Kowalski S. P., Lan T. H., Feldmann K. A., Paterson A. H. Comparative mapping of Arabidopsis thaliana and Brassica oleracea chromosomes reveals islands of conserved organization. Genetics. 1994 Oct;138(2):499–510. doi: 10.1093/genetics/138.2.499. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Lagercrantz U. Comparative mapping between Arabidopsis thaliana and Brassica nigra indicates that Brassica genomes have evolved through extensive genome replication accompanied by chromosome fusions and frequent rearrangements. Genetics. 1998 Nov;150(3):1217–1228. doi: 10.1093/genetics/150.3.1217. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Lagercrantz U., Lydiate D. J. Comparative genome mapping in Brassica. Genetics. 1996 Dec;144(4):1903–1910. doi: 10.1093/genetics/144.4.1903. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Mindrinos M., Katagiri F., Yu G. L., Ausubel F. M. The A. thaliana disease resistance gene RPS2 encodes a protein containing a nucleotide-binding site and leucine-rich repeats. Cell. 1994 Sep 23;78(6):1089–1099. doi: 10.1016/0092-8674(94)90282-8. [DOI] [PubMed] [Google Scholar]
  14. Paterson A. H., Lan T. H., Reischmann K. P., Chang C., Lin Y. R., Liu S. C., Burow M. D., Kowalski S. P., Katsar C. S., DelMonte T. A. Toward a unified genetic map of higher plants, transcending the monocot-dicot divergence. Nat Genet. 1996 Dec;14(4):380–382. doi: 10.1038/ng1296-380. [DOI] [PubMed] [Google Scholar]
  15. Sadowski J., Gaubier P., Delseny M., Quiros C. F. Genetic and physical mapping in Brassica diploid species of a gene cluster defined in Arabidopsis thaliana. Mol Gen Genet. 1996 Jun 12;251(3):298–306. doi: 10.1007/BF02172520. [DOI] [PubMed] [Google Scholar]
  16. Sadowski J., Gaubier P., Delseny M., Quiros C. F. Genetic and physical mapping in Brassica diploid species of a gene cluster defined in Arabidopsis thaliana. Mol Gen Genet. 1996 Jun 12;251(3):298–306. doi: 10.1007/BF02172520. [DOI] [PubMed] [Google Scholar]
  17. 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]
  18. Wroblewski T., Coulibaly S., Sadowski J., Quiros C. F. Variation and phylogenetic utility of the Arabidopsis thaliana Rps2 homolog in various species of the tribe Brassiceae. Mol Phylogenet Evol. 2000 Sep;16(3):440–448. doi: 10.1006/mpev.2000.0781. [DOI] [PubMed] [Google Scholar]
  19. Yang Y. W., Lai K. N., Tai P. Y., Li W. H. Rates of nucleotide substitution in angiosperm mitochondrial DNA sequences and dates of divergence between Brassica and other angiosperm lineages. J Mol Evol. 1999 May;48(5):597–604. doi: 10.1007/pl00006502. [DOI] [PubMed] [Google Scholar]
  20. Zhang M. Q. Identification of protein coding regions in the human genome by quadratic discriminant analysis. Proc Natl Acad Sci U S A. 1997 Jan 21;94(2):565–568. doi: 10.1073/pnas.94.2.565. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Genetics are provided here courtesy of Oxford University Press

RESOURCES