Global analysis of alternative splicing differences between humans and chimpanzees

被引:112
作者
Calarco, John A.
Xing, Yi
Caceres, Mario
Calarco, Joseph P.
Xiao, Xinshu
Pan, Qun
Lee, Christopher
Preuss, Todd M.
Blencowe, Benjamin J. [1 ]
机构
[1] Emory Univ, Dept Pathol, Div Neurosci, Atlanta, GA 30329 USA
[2] Emory Univ, Ctr Behav Neurosci, Yerkes Natl Primate Res Ctr, Atlanta, GA 30329 USA
[3] Univ Toronto, Terrence Donnelly Ctr Cellular & Biomol Res, Banting & Best Dept Med Res, Toronto, ON M5S 3E1, Canada
[4] Univ Toronto, Dept Mol & Med Genet, Toronto, ON M5S 1A8, Canada
[5] Univ Calif Los Angeles, Inst Mol Biol, Ctr Genom & Proteom, Dept Chem & Biochem, Los Angeles, CA 90095 USA
[6] Univ Iowa, Roy J & Lucille A Carver Coll, Dept Internal Med, Iowa City, IA 52242 USA
[7] Univ Iowa, Coll Engn, Dept Biomed Engn, Iowa City, IA 52242 USA
[8] UPF, Ctr Gene Regulat, Genes & Dis Program, Barcelona 08003, Spain
[9] MIT, Dept Biol, Cambridge, MA 02139 USA
关键词
alternative splicing; gene regulation; microarray profiling; primate evolution;
D O I
10.1101/gad.1606907
中图分类号
Q2 [细胞生物学];
学科分类号
071009 [细胞生物学]; 090102 [作物遗传育种];
摘要
Alternative splicing is a powerful mechanism affording extensive proteomic and regulatory diversity from a limited repertoire of genes. However, the extent to which alternative splicing has contributed to the evolution of primate species-specific characteristics has not been assessed previously. Using comparative genomics and quantitative microarray profiling, we performed the first global analysis of alternative splicing differences between humans and chimpanzees. Surprisingly, 6%-8% of profiled orthologous exons display pronounced splicing level differences in the corresponding tissues from the two species. Little overlap is observed between the genes associated with alternative splicing differences and the genes that display steady-state transcript level differences, indicating that these layers of regulation have evolved rapidly to affect distinct subsets of genes in humans and chimpanzees. The alternative splicing differences we detected are predicted to affect diverse functions including gene expression, signal transduction, cell death, immune defense, and susceptibility to diseases. Differences in expression at the protein level of the major splice variant of Glutathione S-transferase omega-2 (GSTO2), which functions in the protection against oxidative stress and is associated with human aging-related diseases, suggests that this enzyme is less active in human cells compared with chimpanzee cells. The results of this study thus support an important role for alternative splicing in establishing differences between humans and chimpanzees.
引用
收藏
页码:2963 / 2975
页数:13
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