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:0
作者
Yajun Cui
Deepti B. Ramnarain
Yueh-Chin Chiang
Liang-Hao Ding
Jeffrey S. McMahon
Clyde L. Denis
机构
[1] Rudman Hall,Department of Biochemistry and Molecular Biology
[2] University of New Hampshire,Simmons Comprehensive Cancer Center Genomics Core Facility
[3] University of Texas Southwestern Medical Center,Division of Molecular Radiation Biology, Department of Radiation Oncology
[4] University of Texas Southwestern Medical Center,undefined
来源
Molecular Genetics and Genomics | 2008年 / 279卷
关键词
CCR4-NOT; SAGA; BTT1; Microarray;
D O I
暂无
中图分类号
学科分类号
摘要
Of the nine known members of the CCR4-NOT complex, CCR4/CAF1 are most important in mRNA deadenylation 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:14
相关论文
共 222 条
  • [1] Albert TK(2002)Identification of a ubiquitin-protein ligase subunit within the CCR4-NOT transcription repressor complex Embo J 21 355-364
  • [2] Hanzawa H(2000)Functional interaction of CCR4-NOT proteins with TATAA-binding protein (TBP) and its associated factors in yeast Genetics 155 1045-1054
  • [3] Legtenberg YI(1999)The CCR4 and CAF1 proteins of the CCR4-NOT complex are physically and functionally separated from NOT2, NOT4, and NOT5 Mol Cell Biol 19 6642-6651
  • [4] de Ruwe MJ(2004)Identification and distinct regulation of yeast TATA box-containing genes Cell 116 699-709
  • [5] van den Heuvel FA(1992)The effects of dNTP pool imbalances on frameshift fidelity during DNA replication J Biol Chem 267 3589-3596
  • [6] Collart MA(1998)Association of distinct yeast Not2 functional domains with components of Gcn5 histone acetylase and Ccr4 transcriptional regulatory complexes Embo J 17 6714-6722
  • [7] Boelens R(2003)Survival of DNA damage in yeast directly depends on increased dNTP levels allowed by relaxed feedback inhibition of ribonucleotide reductase Cell 112 391-401
  • [8] Timmers HT(2002)CCR4, a 3′–5′ poly(A) RNA and ssDNA exonuclease, is the catalytic component of the cytoplasmic deadenylase Embo J 21 1414-1426
  • [9] Badarinarayana V(2001)Purification and characterization of the 1.0 MDa CCR4-NOT complex identifies two novel components of the complex J Mol Biol 314 683-694
  • [10] Chiang YC(1996)The NOT, SPT3, and MOT1 genes functionally interact to regulate transcription at core promoters Mol Cell Biol 16 6668-6676