A Comparison of Whole-Genome Shotgun-Derived Mouse Chromosome 16 and the Human Genome

基因组 同步 生物 人类基因组 遗传学 基因 基因组计划 霰弹枪测序 基因密度 染色体 基因组进化 同源染色体
作者
Richard J. Mural,Mark D. Adams,Eugene W. Myers,Hamilton O. Smith,George L. Gabor Miklos,Ron Wides,Aaron L. Halpern,Peter W. Li,Granger Sutton,Joe Nadeau,Steven L. Salzberg,Robert A. Holt,Chinnappa D. Kodira,Fu Lu,Lin Chen,Zuoming Deng,Carlos Evangelista,Weiniu Gan,Thomas J. Heiman,Jiayin Li,Zhen‐Ya Li,Gennady V. Merkulov,Natalia V. Milshina,Ashwinikumar K Naik,Rong Qi,Bixiong Chris Shue,Aihui Wang,Jian Wang,Xin Wang,Xianghe Yan,Jane J. Ye,Shibu Yooseph,Qi Zhao,Liansheng Zheng,Shiaoping C. Zhu,Kendra Biddick,Randall Bolanos,Arthur L. Delcher,Ian Dew,Daniel Fasulo,Michael J. Flanigan,Daniel H. Huson,Saul Kravitz,Jason R. Miller,Clark Mobarry,Knut Reinert,Karin Remington,Qing Zhang,Xiangqun H. Zheng,Deborah Nusskern,Zhongwu Lai,Yiding Lei,Wenyan Zhong,Alison Yao,Peng Guan,Rui-Ru Ji,Zhiping Gu,Zhenyuan Wang,Fei Zhong,Chunlin Xiao,Chia-Chien Chiang,Mark Yandell,Jennifer Wortman,P. G. Amanatides,Suzanne L Hladun,Eric C Pratts,Jeffery E Johnson,Kristina L Dodson,Kerry J. Woodford,Cheryl Evans,Barry Gropman,Douglas B. Rusch,Eli Venter,Mei Wang,Thomas J. Smith,Jarrett T Houck,Donald E Tompkins,Charles A. Haynes,Debbie Jacob,Soo H Chin,David R. Allen,Carl Dahlke,Robert D. Sanders,Kelvin Li,Xiangjun Liu,Alexander Levitsky,William H. Majoros,Quan Chen,Ashley C Xia,John Lopez,Michael Donnelly,Matthew Newman,Anna Glodek,Cheryl Kraft,Marc Nodell,Feroze Ali,Hui-Jin An,Danita Baldwin-Pitts,Karen Beeson,Shuang Cai
出处
期刊:Science [American Association for the Advancement of Science (AAAS)]
卷期号:296 (5573): 1661-1671 被引量:355
标识
DOI:10.1126/science.1069193
摘要

The high degree of similarity between the mouse and human genomes is demonstrated through analysis of the sequence of mouse chromosome 16 (Mmu 16), which was obtained as part of a whole-genome shotgun assembly of the mouse genome. The mouse genome is about 10% smaller than the human genome, owing to a lower repetitive DNA content. Comparison of the structure and protein-coding potential of Mmu 16 with that of the homologous segments of the human genome identifies regions of conserved synteny with human chromosomes (Hsa) 3, 8, 12, 16, 21, and 22. Gene content and order are highly conserved between Mmu 16 and the syntenic blocks of the human genome. Of the 731 predicted genes on Mmu 16, 509 align with orthologs on the corresponding portions of the human genome, 44 are likely paralogous to these genes, and 164 genes have homologs elsewhere in the human genome; there are 14 genes for which we could find no human counterpart.
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