Stiller John W, Hall Benjamin D
Department of Biology, East Carolina University, Greenville, NC 27858, USA.
Proc Natl Acad Sci U S A. 2002 Apr 30;99(9):6091-6. doi: 10.1073/pnas.082646199. Epub 2002 Apr 23.
In recent years a great deal of biochemical and genetic research has focused on the C-terminal domain (CTD) of the largest subunit (RPB1) of DNA-dependent RNA polymerase II. This strongly conserved domain of tandemly repeated heptapeptides has been linked functionally to important steps in the initiation and processing of mRNA transcripts in both animals and fungi. Although they are absolutely required for viability in these organisms, C-terminal tandem repeats do not occur in RPB1 sequences from diverse eukaryotic taxa. Here we present phylogenetic analyses of RPB1 sequences showing that canonical CTD heptads are strongly conserved in only a subset of eukaryotic groups, all apparently descended from a single common ancestor. Moreover, eukaryotic groups in which the most complex patterns of ontogenetic development occur are descended from this CTD-containing ancestor. Consistent with the results of genetic and biochemical investigations of CTD function, these analyses suggest that the enhanced control over RNA polymerase II transcription conveyed by acquired CTD/protein interactions was an important step in the evolution of intricate patterns of gene expression that are a hallmark of large, developmentally complex eukaryotic organisms.
近年来,大量的生物化学和遗传学研究聚焦于依赖DNA的RNA聚合酶II最大亚基(RPB1)的C末端结构域(CTD)。这个由串联重复七肽组成的高度保守结构域在功能上与动物和真菌中mRNA转录本的起始和加工的重要步骤相关联。尽管这些串联重复序列对于这些生物体的生存绝对必要,但在不同真核生物类群的RPB1序列中并未出现C末端串联重复序列。在此,我们展示了RPB1序列的系统发育分析,结果表明典型的CTD七联体仅在一部分真核生物类群中高度保守,所有这些类群显然都起源于一个共同祖先。此外,个体发育最复杂模式出现的真核生物类群都起源于这个含有CTD的祖先。与CTD功能的遗传和生物化学研究结果一致,这些分析表明,通过获得的CTD/蛋白质相互作用对RNA聚合酶II转录增强的控制是复杂基因表达模式进化中的一个重要步骤,而这种复杂基因表达模式是大型、发育复杂的真核生物的一个标志。