Egloff Sylvain, Murphy Shona
Sir William Dunn School of Pathology, University of Oxford, South Parks Road, Oxford OX1 3RE, UK.
Biochem Soc Trans. 2008 Jun;36(Pt 3):537-9. doi: 10.1042/BST0360537.
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.
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。