Role of the mammalian RNA polymerase IIC-terminal domain (CTD) nonconsensus repeats in CTD stability and cell proliferation

被引:48
作者
Chapman, RD [1 ]
Conrad, M [1 ]
Eick, D [1 ]
机构
[1] GSF Munich, Inst Klin Mol Biol & Tumor Genet, Hematologikum, Ctr Environm & Hlth, D-81377 Munich, Germany
关键词
D O I
10.1128/MCB.25.17.7665-7674.2005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The C-terminal domain (CTD) of mammalian RNA polymerase II (Pol II) consists of 52 repeats of the consensus heptapeptide YSPTSPS and links transcription to the processing of pre-mRNA. The length of the CTD and the number of repeats diverging from the consensus sequence have increased through evolution, but their functional importance remains unknown. Here, we show that the deletion of repeats I to 3 or 52 leads to cleavage and degradation of the CTD from Pol II in vivo. Including these repeats, however, allowed the construction of stable, synthetic CTDs. To our surprise, polymerases consisting of just consensus repeats could support normal growth and viability of cells. We conclude that all other nonconsensus CTD repeats are dispensable for the transcription and pre-mRNA processing of genes essential for proliferation.
引用
收藏
页码:7665 / 7674
页数:10
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