期刊文献+

Long-term maintenance of stable copy number in the eukaryotic SMC family: origin of a vertebrate meiotic SMC1 and fate of recent segmental duplicates 被引量:2

Long-term maintenance of stable copy number in the eukaryotic SMC family: origin of a vertebrate meiotic SMC1 and fate of recent segmental duplicates
下载PDF
导出
摘要 Members of the Structural Maintenance of Chromosome (SMC) family have long been of interest to molecular and evolutionary biologists for their role in chromosome structural dynamics, particularly sister chro-matid cohesion, condensation, and DNA repair. SMC and related proteins are found in all major groups of living organisms and share a common structure of conserved N and C globular domains separated from the conserved hinge domain by long coiled-coil regions. In eukaryotes there are six paralogous proteins that form three het-erodimeric pairs, whereas in prokaryotes there is only one SMC protein that homodimerizes. From recently com-pleted genome sequences, we have identified SMC genes from 34 eukaryotes that have not been described in previous reports. Our phylogenetic analysis of these and previously identified SMC genes supports an origin for the vertebrate meiotic SMC1 in the most recent common ancestor since the divergence from invertebrate animals. Additionally, we have identified duplicate copies due to segmental duplications for some of the SMC paralogs in plants and yeast, mainly SMC2 and SMC6, and detected evidence that duplicates of other paralogs were lost, suggesting differential evolution for these genes. Our analysis indicates that the SMC paralogs have been stably maintained at very low copy numbers, even after segmental (genome-wide) duplications. It is possible that such low copy numbers might be selected during eukaryotic evolution, although other possibilities are not ruled out. Members of the Structural Maintenance molecular and evolutionary biologists for their role of Chromosome (SMC) family have long been of interest to in chromosome structural dynamics, particularly sister chromatid cohesion, condensation, and DNA repair. SMC and related proteins are found in all major groups of living organisms and share a common structure of conserved N and C globular domains separated from the conserved hinge domain by long coiled-coil regions. In eukaryotes there are six paralogous proteins that form three heterodimeric pairs, whereas in prokaryotes there is only one SMC protein that homodimerizes. From recently completed genome sequences, we have identified SMC genes from 34 eukaryotes that have not been described in previous reports. Our phylogenetic analysis of these and previously identified SMC genes supports an origin for the vertebrate meiotic SMC1 in the most recent common ancestor since the divergence from invertebrate animals. Additionally, we have identified duplicate copies due to segmental duplications for some of the SMC paralogs in plants and yeast, mainly SMC2 and SMC6, and detected evidence that duplicates of other paralogs were lost, suggesting differential evolution for these genes. Our analysis indicates that the SMC paralogs have been stably maintained at very low copy numbers, even after segmental (genome-wide) duplications. It is possible that such low copy numbers might be selected during eukaryotic evolution, although other possibilities are not ruled out.
出处 《植物分类学报》 CSCD 北大核心 2008年第3期405-423,共19页 Acta Phytotaxonomica Sinica
关键词 真核 脊椎动物 减数分裂 细胞 cohesin, condensin, meiosis, segmental duplication, SMC.
  • 相关文献

参考文献20

  • 1Adams KL, Wendel JF. 2005. Polyploidy and genome evolution in plants. Current Opinions in Plant Biology 8: 135-141.
  • 2Beasley M, Xu H, Warren W, McKay M. 2002. Conserved disruptions in the predicted coiled-coil domains of eukaryotic SMC complexes: implications for structure and function. Genome Research 12:1201-1209.
  • 3Cobbe N, Heck MM. 2004. The evolution of SMC proteins: phylogenetic analysis and structural implications. Molecular Biology and Evolution 21: 332-347.
  • 4Deardorff MA, Kaur M, Yaeger D, Rampuria A, Korolev S, Pie J, Gil-Rodriquez C, Arnedo M, Loeys B, Kline AD, Wilson M, Lillquist K, Siu V, Ramos F J, Musio A,Jackson LS, Dorsett D, Krantz ID. 2007. Mutations in cohesin complex members SMC3 and SMC1A cause a mild variant of Cornelia de Lange syndrome with predominant mental retardation. The American Journal of Human Genetics 80: 485-494.
  • 5Dong F, Cai X, Makaroff CA. 2001. Cloning and characterization of two Arabidopsis genes that belong to the RAD21/REC8 family of chromosome cohesin proteins. Gene 271: 99-108.
  • 6Edger RC. 2004. MUSCLE: a multiple sequence alignment method with reduced time and space complexity [online]. BMC Bioinformatics 5: 113. doi:10.1186/1471-2105-5-113. Available from http://www.biomedcentral.com [accessed 5 March 2008].
  • 7Eijpe M, Heyting C, Gross B, Jessberger R. 2000. Association of mammalian SMC1 and SMC3 proteins with meiotic chromosomes and synaptonemal complexes. Journal of Cell Science 113: 673-683.
  • 8Gilliland WD, Hawley RS. 2005. Cohesin and the maternal age effect. Cell 123: 371-373.
  • 9Guindon S, Gascuel O. 2003. PhyML--A simple, fast, and accurate algorithm to estimate large phylogenies by maximum likelihood. Systematic Biology 52: 696-704.
  • 10Hirano T. 2002. The ABCs of SMC proteins: two-armed ATPases for chromosome condensation, cohesion, and repair. Genes & Development 16: 399-414.

同被引文献2

引证文献2

二级引证文献4

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部