Insights into the structure and architecture of the CCR4-NOT complex

被引:30
作者
Xu, Kun [1 ,2 ]
Bai, Yuwei [1 ]
Zhang, Aili [1 ,2 ]
Zhang, Qionglin [2 ]
Bartlam, Mark G. [1 ,2 ]
机构
[1] Nankai Univ, State Key Lab Med Chem Biol, Tianjin 300071, Peoples R China
[2] Nankai Univ, Coll Life Sci, Tianjin 300071, Peoples R China
关键词
MESSENGER-RNA DEADENYLATION; SACCHAROMYCES-CEREVISIAE; TRANSCRIPTION FACTOR; GENE-EXPRESSION; DIFFERENTIALLY AFFECTS; CRYSTAL-STRUCTURE; BINDING PROTEIN; NUCLEASE MODULE; CAF1; PROTEINS; YEAST;
D O I
10.3389/fgene.2014.00137
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The CCR4-NOT complex is a highly conserved, multifunctional machinery with a general role in controlling mRNA metabolism. It has been implicated in a number of different aspects of mRNA and protein expression, including mRNA degradation, transcription initiation and elongation, ubiquitination, and protein modification. The core CCR4-NOT complex is evolutionarily conserved and consists of at least three NOT proteins and two catalytic subunits. The L-shaped complex is characterized by two functional modules bound to the CNOT1/Not1 scaffold protein: the deadenylase or nuclease module containing two enzymes required for deadenylation, and the NOT module. In this review, we will summarize the currently available information regarding the three-dimensional structure and assembly of the CCR4-NOT complex, in order to provide insight into its roles in mRNA degradation and other biological processes.
引用
收藏
页数:12
相关论文
共 70 条
[1]   Identification of a ubiquitin-protein ligase subunit within the CCR4-NOT transcription repressor complex [J].
Albert, TK ;
Hanzawa, H ;
Legtenberg, YIA ;
de Ruwe, MJ ;
van den Heuvel, FAJ ;
Collart, MA ;
Boelens, R ;
Timmers, HTM .
EMBO JOURNAL, 2002, 21 (03) :355-364
[2]   Isolation and characterization of human orthologs of yeast CCR4-NOT complex subunits [J].
Albert, TK ;
Lemaire, M ;
van Berkum, NL ;
Gentz, R ;
Collart, MA ;
Timmers, HTM .
NUCLEIC ACIDS RESEARCH, 2000, 28 (03) :809-817
[3]   The activity and selectivity of fission yeast Pop2p are affected by a high affinity for Zn2+ and Mn2+ in the active site [J].
Andersen, Kasper Rojkjaer ;
Jonstrup, Anette Thyssen ;
Van, Lan Bich ;
Brodersen, Ditlev Egeskov .
RNA, 2009, 15 (05) :850-861
[4]   The Ccr4-Not Deadenylase Subunits CNOT7 and CNOT8 Have Overlapping Roles and Modulate Cell Proliferation [J].
Aslam, Akhmed ;
Mittal, Saloni ;
Koch, Frederic ;
Andrau, Jean-Christophe ;
Winkler, G. Sebastiaan .
MOLECULAR BIOLOGY OF THE CELL, 2009, 20 (17) :3840-3850
[5]  
Badarinarayana V, 2000, GENETICS, V155, P1045
[6]  
Bai YL, 1999, MOL CELL BIOL, V19, P6642
[7]   The structural basis for deadenylation by the CCR4-NOT complex [J].
Bartlam, Mark ;
Yamamoto, Tadashi .
PROTEIN & CELL, 2010, 1 (05) :443-452
[8]   Architecture of the Nuclease Module of the Yeast Ccr4-Not Complex: the Not1-Caf1-Ccr4 Interaction [J].
Basquin, Jerome ;
Roudko, Vladimir V. ;
Rode, Michaela ;
Basquin, Claire ;
Seraphin, Bertrand ;
Conti, Elena .
MOLECULAR CELL, 2012, 48 (02) :207-218
[9]   NOT10 and C2orf29/NOT11 form a conserved module of the CCR4-NOT complex that docks onto the NOT1 N-terminal domain [J].
Bawankar, Praveen ;
Loh, Belinda ;
Wohlbold, Lara ;
Schmidt, Steffen ;
Izaurralde, Elisa .
RNA BIOLOGY, 2013, 10 (02) :228-244
[10]   Association of distinct yeast Not2 functional domains with components of Gcn5 histone acetylase and Ccr4 transcriptional regulatory complexes [J].
Benson, JD ;
Benson, M ;
Howley, PM ;
Struhl, K .
EMBO JOURNAL, 1998, 17 (22) :6714-6722