Calarco John A, Xing Yi, Cáceres Mario, Calarco Joseph P, Xiao Xinshu, Pan Qun, Lee Christopher, Preuss Todd M, Blencowe Benjamin J
Banting and Best Department of Medical Research, University of Toronto, Terrence Donnelly Center for Cellular and Biomolecular Research, Toronto, Ontario M5S 3E1, Canada.
Genes Dev. 2007 Nov 15;21(22):2963-75. doi: 10.1101/gad.1606907. Epub 2007 Oct 31.
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.
可变剪接是一种强大的机制,能从有限的基因库中产生广泛的蛋白质组和调控多样性。然而,此前尚未评估可变剪接对灵长类物种特异性特征进化的贡献程度。我们利用比较基因组学和定量微阵列分析,首次对人类和黑猩猩之间的可变剪接差异进行了全面分析。令人惊讶的是,6% - 8%的已分析直系同源外显子在两个物种的相应组织中表现出明显的剪接水平差异。在与可变剪接差异相关的基因和显示稳态转录水平差异的基因之间几乎没有重叠,这表明这些调控层面已迅速进化,以影响人类和黑猩猩中不同的基因子集。我们检测到的可变剪接差异预计会影响多种功能,包括基因表达、信号转导、细胞死亡、免疫防御以及疾病易感性。谷胱甘肽S - 转移酶ω-2(GSTO2)的主要剪接变体在蛋白质水平上的表达差异,该酶在抗氧化应激中起作用并与人类衰老相关疾病有关,这表明与黑猩猩细胞相比,这种酶在人类细胞中的活性较低。因此,本研究结果支持可变剪接在人类和黑猩猩之间建立差异中发挥重要作用。