Liu Shuo, Altman Russ B
Department of Genetics, Stanford Medical Informatics, 251 Campus Drive, MSOB X-215, Stanford, CA 94305-5479, USA.
Nucleic Acids Res. 2003 Aug 15;31(16):4828-35. doi: 10.1093/nar/gkg668.
Alternative splicing plays an important role in processes such as development, differentiation and cancer. With the recent increase in the estimates of the number of human genes that undergo alternative splicing from 5 to 35-59%, it is becoming critical to develop a better understanding of its functional consequences and regulatory mechanisms. We conducted a large scale study of the distribution of protein domains in a curated data set of several thousand genes and identified protein domains disproportionately distributed among alternatively spliced genes. We also identified a number of protein domains that tend to be spliced out. Both the proteins having the disproportionately distributed domains as well as those with spliced-out domains are predominantly involved in the processes of cell communication, signaling, development and apoptosis. These proteins function mostly as enzymes, signal transducers and receptors. Somewhat surprisingly, 28% of all occurrences of spliced-out domains are not effected by straightforward exclusion of exons coding for the domains but by inclusion or exclusion of other exons to shift the reading frame while retaining the exons coding for the domains in the final transcripts.
可变剪接在发育、分化和癌症等过程中发挥着重要作用。随着最近对经历可变剪接的人类基因数量估计的增加,从5%增至35%-59%,深入了解其功能后果和调控机制变得至关重要。我们对数千个基因的精选数据集进行了蛋白质结构域分布的大规模研究,并确定了在可变剪接基因中分布不均衡的蛋白质结构域。我们还鉴定出了一些倾向于被剪接掉的蛋白质结构域。具有分布不均衡结构域的蛋白质以及具有被剪接掉结构域的蛋白质主要参与细胞通讯、信号传导、发育和细胞凋亡过程。这些蛋白质大多作为酶、信号转导器和受体发挥作用。有点令人惊讶的是,所有被剪接掉结构域的情况中,有28%并非通过直接排除编码这些结构域的外显子来实现,而是通过包含或排除其他外显子来改变阅读框,同时在最终转录本中保留编码这些结构域的外显子。