Genome wide expression analysis of the CCR4-NOT complex indicates that it consists of three modules with the NOT module controlling SAGA-responsive genes

被引:48
作者
Cui, Yajun [1 ]
Ramnarain, Deepti B. [1 ]
Chiang, Yueh-Chin [1 ]
Ding, Liang-Hao [2 ,3 ]
McMahon, Jeffrey S. [1 ]
Denis, Clyde L. [1 ]
机构
[1] Univ New Hampshire, Dept Biochem & Mol Biol, Durham, NH 03824 USA
[2] Univ Texas SW Med Ctr Dallas, Simmons Comprehens Canc Ctr Genom Core Facil, Dallas, TX 75390 USA
[3] Univ Texas SW Med Ctr Dallas, Dept Radiat Oncol, Div Mol Radiat Biol, Dallas, TX USA
关键词
CCR4-NOT; SAGA; BTT1; microarray;
D O I
10.1007/s00438-007-0314-1
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
Of the nine known members of the CCR4-NOT complex, CCR4/CAF1 are most important in mRNA dead-enylation whereas the NOT1-5 proteins are most critical for transcriptional repression. Whole genome microarray analysis using deletions in seven of the CCR4-NOT genes was used to determine the overall mRNA expression patterns that are affected by members of the yeast CCR4-NOT complex. Under glucose conditions, ccr4 and caf1 displayed a high degree of similarity in the manner that they affected gene expression. In contrast, the not deletions were similar in the way they affected genes, but showed no correlation with that of ccr4/caf1. A number of groups of functionally related proteins were specifically controlled by the CCR4/ CAF1 or NOT modules. Importantly, the NOT proteins preferentially affected SAGA-controlled gene expression. Also, both the CCR4/CAF1 and NOT group of proteins shared much greater similarities in their effects on gene expression during the stress of glucose deprivation. BTT1, a member of the nascent polypeptide association complex that binds the ribosome, was shown to be a tenth member of the CCR4-NOT complex, interacting through CAF130. Microarray analysis indicated that BTT1 and CAF130 correlate very highly in their control of gene expression and preferentially repress genes involved in ribosome biogenesis. These results indicate that distinct portions of the CCR4-NOT complex control a number of different cellular processes.
引用
收藏
页码:323 / 337
页数:15
相关论文
共 51 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]  
Badarinarayana V, 2000, GENETICS, V155, P1045
[3]  
Bai YL, 1999, MOL CELL BIOL, V19, P6642
[4]   Identification and distinct regulation of yeast TATA box-containing genes [J].
Basehoar, AD ;
Zanton, SJ ;
Pugh, BF .
CELL, 2004, 116 (05) :699-709
[5]  
BEBENEK K, 1992, J BIOL CHEM, V267, P3589
[6]   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
[7]   Survival of DNA damage in yeast directly depends on increased dNTP levels allowed by relaxed feedback inhibition of ribonucleotide reductase [J].
Chabes, A ;
Georgieva, B ;
Domkin, V ;
Zhao, XL ;
Rothstein, R ;
Thelander, L .
CELL, 2003, 112 (03) :391-401
[8]   Purification and characterization of the 1.0 MDa CCR4-NOT complex identifies two novel components of the complex [J].
Chen, JJ ;
Rappsilber, J ;
Chiang, YC ;
Russell, P ;
Mann, M ;
Denis, CL .
JOURNAL OF MOLECULAR BIOLOGY, 2001, 314 (04) :683-694
[9]   CCR4, a 3′-5′ poly(A) RNA and ssDNA exonuclease, is the catalytic component of the cytoplasmic deadenylase [J].
Chen, JJ ;
Chiang, YC ;
Denis, CL .
EMBO JOURNAL, 2002, 21 (06) :1414-1426
[10]   The eukaryotic Ccr4-Not complex: A regulatory platform integrating mRNA metabolism with cellular signaling pathways? [J].
Collart, MA ;
Timmers, HTM .
PROGRESS IN NUCLEIC ACID RESEARCH AND MOLECULAR BIOLOGY, VOL 77, 2004, 77 :289-322