The structural basis for deadenylation by the CCR4-NOT complex.
10.1007/s13238-010-0060-8
- Author:
Mark BARTLAM
1
;
Tadashi YAMAMOTO
Author Information
1. Tianjin Key Laboratory of Protein Science, College of Life Sciences, Nankai University, Tianjin 300071, China. bartlam@nankai.edu.cn
- Publication Type:Journal Article
- MeSH:
Animals;
Humans;
Multiprotein Complexes;
chemistry;
genetics;
metabolism;
Protein Conformation;
RNA, Messenger;
genetics;
metabolism;
Transcription Factors;
chemistry;
genetics;
metabolism
- From:
Protein & Cell
2010;1(5):443-452
- CountryChina
- Language:English
-
Abstract:
The CCR4-NOT complex is a highly conserved, multifunctional machinery controlling mRNA metabolism. Its components have been implicated in several aspects of mRNA and protein expression, including transcription initiation, elongation, mRNA degradation, ubiquitination, and protein modification. In this review, we will focus on the role of the CCR4-NOT complex in mRNA degradation. The complex contains two types of deadenylase enzymes, one belonging to the DEDD-type family and one belonging to the EEP-type family, which shorten the poly(A) tails of mRNA. We will review the present state of structure-function analyses into the CCR4-NOT deadenylases and summarize current understanding of their roles in mRNA degradation. We will also review structural and functional work on the Tob/BTG family of proteins, which are known to interact with the CCR4-NOT complex and which have been reported to suppress deadenylase activity in vitro.
