Cracking the RNA polymerase IICTD code

被引:298
作者
Egloff, Sylvain [1 ]
Murphy, Shona [1 ]
机构
[1] Univ Oxford, Sir William Dunn Sch Pathol, Oxford OX1 3RE, England
基金
英国医学研究理事会;
关键词
D O I
10.1016/j.tig.2008.03.008
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The carboxyl-terminal domain (CTD) of the largest subunit of RNA polymerase II comprises multiple tandem conserved heptapeptide repeats, unique to this eukaryotic RNA polymerase. This unusual structure provides a docking platform for factors involved in various co-transcriptional events. Recruitment of the appropriate factors at different stages of the transcription cycle is achieved through changing patterns of post-translational modification of the CTD repeats, which create a readable 'code'. A new phosphorylation mark both expands the CTD code and provides the first example of a CTD signal read in a gene type-specific manner. How and when is the code written and read? How does it contribute to transcription and coordinate RNA processing?.
引用
收藏
页码:280 / 288
页数:9
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