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The RNA polymerase II CTD 'orphan' residues: Emerging insights into the functions of Tyr-1, Thr-4, and Ser-7

机译:RNA聚合酶II CTD“孤儿”残基:出现洞察Tyr-1,Thr-4和Ser-7功能的见解

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摘要

The C-terminal domain (CTD) of the RNA polymerase II largest subunit consists of a unique repeated heptad sequence of the consensus Tyr1-Ser2-Pro3-Thr4-Ser5-Pro6-Ser7. An important function of the CTD is to couple transcription with RNA processing reactions that occur during the initiation, elongation, and termination phases of transcription. During this transcription cycle, the CTD is subject to extensive modification, primarily phosphorylation, on its non-proline residues. Reversible phosphorylation of Ser2 and Ser5 is well known to play important and general functions during transcription in all eukaryotes. More recent studies have enhanced our understanding of Tyr1, Thr4, and Ser7, and what have been previously characterized as unknown or specialized functions for these residues has changed to a more fine-detailed map of transcriptional regulation that highlights similarities as well as significant differences between organisms. Here, we review recent findings on the function and modification of these three residues, which further illustrate the importance of the CTD in precisely modulating gene expression.
机译:RNA聚合酶II最大亚基的C-末端结构域(CTD)由共有型TYR1-SER2-PRO3-THR4-SER5-PRO6-SER7的独特的重复七肽组成。 CTD的一个重要功能是将转录与RNA处理反应的转录耦合,所述RNA处理反应在转录的开始,伸长和终止阶段发生。在该转录周期期间,CTD在其非脯氨酸残基上进行广泛的修饰,主要是磷酸化。众所周知,Ser2和Ser5的可逆磷酸化是在所有真核生物中转录过程中的重要和一般功能。最近的研究提高了我们对Tyr1,Thr4和Ser7的理解,以前所表征为这些残留物的未知或专业功能已经改变为更精细的转录规则图,突出了相似之处以及之间的显着差异生物。在这里,我们审查了最近关于这三个残基的功能和修饰的发现,这进一步说明了CTD在精确调节基因表达中的重要性。

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