Krull Maren, Brosius Jürgen, Schmitz Jürgen
Institute of Experimental Pathology (ZMBE), University of Münster, Münster, Germany.
Mol Biol Evol. 2005 Aug;22(8):1702-11. doi: 10.1093/molbev/msi164. Epub 2005 May 18.
The majority of more than one million primate-specific Alu elements map to nonfunctional parts of introns or intergenic sequences. Once integrated, they have the potential to become exapted as functional modules, e.g., as protein-coding domains via alternative splicing. This particular process is also termed exonization and increases protein versatility. Here we investigate 153 human chromosomal loci where Alu elements were conceivably exonized. In four selected examples, we generated, with the aid of representatives of all primate infraorders, phylogenetic reconstructions of the evolutionary steps presumably leading to exonization of Alu elements. We observed a variety of possible scenarios in which Alu elements led to novel mRNA splice forms and which, like most evolutionary processes, took different courses in different lineages. Our data show that, once acquired, some exonizations were lost again in some lineages. In general, Alu exonization occurred at various time points over the evolutionary history of primate lineages, and protein-coding potential was acquired either relatively soon after integration or millions of years thereafter. The course of these paths can probably be generalized to the exonization of other elements as well.
超过100万个灵长类特有的Alu元件中的大多数定位于内含子的非功能部分或基因间序列。一旦整合,它们就有可能被适应性地用作功能模块,例如,通过可变剪接作为蛋白质编码结构域。这个特定过程也被称为外显子化,并增加了蛋白质的多样性。在这里,我们研究了153个人类染色体位点,在这些位点上Alu元件可能被外显子化。在四个选定的例子中,我们借助所有灵长类下目的代表,对可能导致Alu元件外显子化的进化步骤进行了系统发育重建。我们观察到了多种可能的情况,其中Alu元件导致了新的mRNA剪接形式,并且与大多数进化过程一样,在不同的谱系中采取了不同的路径。我们的数据表明,一旦获得,一些外显子化在某些谱系中又会再次丢失。一般来说,Alu外显子化发生在灵长类谱系进化历史的不同时间点,并且蛋白质编码潜力要么在整合后相对较快获得,要么在数百万年后获得。这些路径的过程可能也可以推广到其他元件的外显子化。