Inferring nonneutral evolution from human-chimp-mouse orthologous gene trios

被引:487
作者
Clark, AG
Glanowski, S
Nielsen, R
Thomas, PD
Kejariwal, A
Todd, MA
Tanenbaum, DM
Civello, D
Lu, F
Murphy, B
Ferriera, S
Wang, G
Zheng, XG
White, TJ
Sninsky, JJ
Adams, MD
Cargill, M
机构
[1] Celera Diagnost, Alameda, CA 94502 USA
[2] Cornell Univ, Ithaca, NY 14853 USA
[3] Appl Biosyst Inc, Rockville, MD 20850 USA
[4] Celera Genom, Prot Informat, Foster City, CA 94404 USA
[5] Celera Genom, Rockville, MD 20850 USA
关键词
D O I
10.1126/science.1088821
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Even though human and chimpanzee gene sequences are nearly 99% identical, sequence comparisons can nevertheless be highly informative in identifying biologically important changes that have occurred since our ancestral lineages diverged. We analyzed alignments of 7645 chimpanzee gene sequences to their human and mouse orthologs. These three-species sequence alignments allowed us to identify genes undergoing natural selection along the human and chimp lineage by fitting models that include parameters specifying rates of synonymous and nonsynonymous nucleotide substitution. This evolutionary approach revealed an informative set of genes with significantly different patterns of substitution on the human lineage compared with the chimpanzee and mouse lineages. Partitions of genes into inferred biological classes identified accelerated evolution in several functional classes, including olfaction and nuclear transport. In addition to suggesting adaptive physiological differences between chimps and humans, human-accelerated genes are significantly more likely to underlie major known Mendelian disorders.
引用
收藏
页码:1960 / 1963
页数:4
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