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RNA聚合酶II的C末端结构域在小核RNA基因表达中的作用。

Role of the C-terminal domain of RNA polymerase II in expression of small nuclear RNA genes.

作者信息

Egloff Sylvain, Murphy Shona

机构信息

Sir William Dunn School of Pathology, University of Oxford, South Parks Road, Oxford OX1 3RE, UK.

出版信息

Biochem Soc Trans. 2008 Jun;36(Pt 3):537-9. doi: 10.1042/BST0360537.

DOI:10.1042/BST0360537
PMID:18482001
Abstract

Pol II (RNA polymerase II) transcribes the genes encoding proteins and non-coding snRNAs (small nuclear RNAs). The largest subunit of Pol II contains a distinctive CTD (C-terminal domain) comprising a repetitive heptad amino acid sequence, Tyr(1)-Ser(2)-Pro(3)-Thr(4)-Ser(5)-Pro(6)-Ser(7). This domain is now known to play a major role in the processes of transcription and co-transcriptional RNA processing in expression of both snRNA and protein-coding genes. The heptapeptide repeat unit can be extensively modified in vivo and covalent modifications of the CTD during the transcription cycle result in the ordered recruitment of RNA-processing factors. The most studied modifications are the phosphorylation of the serine residues in position 2 and 5 (Ser(2) and Ser(5)), which play an important role in the co-transcriptional processing of both mRNA and snRNA. An additional, recently identified CTD modification, phosphorylation of the serine residue in position 7 (Ser(7)) of the heptapeptide, is however specifically required for expression of snRNA genes. These findings provide interesting insights into the control of gene-specific Pol II function.

摘要

RNA聚合酶II(Pol II)转录编码蛋白质和非编码小核RNA(snRNA)的基因。Pol II的最大亚基包含一个独特的C端结构域(CTD),其由重复的七肽氨基酸序列Tyr(1)-Ser(2)-Pro(3)-Thr(4)-Ser(5)-Pro(6)-Ser(7)组成。现在已知该结构域在snRNA和蛋白质编码基因表达的转录及共转录RNA加工过程中起主要作用。七肽重复单元在体内可被广泛修饰,转录周期中CTD的共价修饰导致RNA加工因子的有序募集。研究最多的修饰是第2位和第5位丝氨酸残基(Ser(2)和Ser(5))的磷酸化,它们在mRNA和snRNA的共转录加工中起重要作用。然而,七肽第7位丝氨酸残基(Ser(7))的磷酸化这一最近发现的CTD额外修饰,是snRNA基因表达所特需的。这些发现为基因特异性Pol II功能的调控提供了有趣的见解。