Literature DB >> 10490603

The CCR4 and CAF1 proteins of the CCR4-NOT complex are physically and functionally separated from NOT2, NOT4, and NOT5.

Y Bai1, C Salvadore, Y C Chiang, M A Collart, H Y Liu, C L Denis.   

Abstract

The CCR4-NOT complex (1 mDa in size), consisting of the proteins CCR4, CAF1, and NOT1 to NOT5, regulates gene expression both positively and negatively and is distinct from other large transcriptional complexes in Saccharomyces cerevisiae such as SNF/SWI, TFIID, SAGA, and RNA polymerase II holoenzyme. The physical and genetic interactions between the components of the CCR4-NOT complex were investigated in order to gain insight into how this complex affects the expression of diverse genes and processes. The CAF1 protein was found to be absolutely required for CCR4 association with the NOT proteins, and CCR4 and CAF1, in turn, physically interacted with NOT1 through its central amino acid region from positions 667 to 1152. The NOT3, NOT4, and NOT5 proteins had no significant effect on the association of CCR4, CAF1, and NOT1 with each other. In contrast, the NOT2, NOT4, and NOT5 interacted with the C-terminal region (residues 1490 to 2108) of NOT1 in which NOT2 and NOT5 physically associated in the absence of CAF1, NOT3, and NOT4. These and other data indicate that the physical ordering of these proteins in the complex is CCR4-CAF1-NOT1-(NOT2, NOT5), with NOT4 and NOT3 more peripheral to NOT2 and NOT5. The physical separation of CCR4 and CAF1 from other components of the CCR4-NOT complex correlated with genetic analysis indicating partially separate functions for these two groups of proteins. ccr4 or caf1 deletion suppressed the increased 3-aminotriazole resistance phenotype conferred by not mutations, resulted in opposite effects on gene expression as compared to several not mutations, and resulted in a number of synthetic phenotypes in combination with not mutations. These results define the CCR4-NOT complex as consisting of at least two physically and functionally separated groups of proteins.

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Year:  1999        PMID: 10490603      PMCID: PMC84645          DOI: 10.1128/MCB.19.10.6642

Source DB:  PubMed          Journal:  Mol Cell Biol        ISSN: 0270-7306            Impact factor:   4.272


  24 in total

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Authors:  H Y Liu; J H Toyn; Y C Chiang; M P Draper; L H Johnston; C L Denis
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Authors:  M Chang; D French-Cornay; H Y Fan; H Klein; C L Denis; J A Jaehning
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Journal:  Mol Cell Biol       Date:  1990-06       Impact factor: 4.272

4.  The CCR4 gene from Saccharomyces cerevisiae is required for both nonfermentative and spt-mediated gene expression.

Authors:  C L Denis; T Malvar
Journal:  Genetics       Date:  1990-02       Impact factor: 4.562

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Authors:  S I Komarnitsky; Y C Chiang; F C Luca; J Chen; J H Toyn; M Winey; L H Johnston; C L Denis
Journal:  Mol Cell Biol       Date:  1998-04       Impact factor: 4.272

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Authors:  M A Collart; K Struhl
Journal:  EMBO J       Date:  1993-01       Impact factor: 11.598

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  80 in total

1.  CCR4, a 3'-5' poly(A) RNA and ssDNA exonuclease, is the catalytic component of the cytoplasmic deadenylase.

Authors:  Junji Chen; Yueh-Chin Chiang; Clyde L Denis
Journal:  EMBO J       Date:  2002-03-15       Impact factor: 11.598

2.  Identification of a ubiquitin-protein ligase subunit within the CCR4-NOT transcription repressor complex.

Authors:  Thomas K Albert; Hiroyuki Hanzawa; Yvonne I A Legtenberg; Marjolein J de Ruwe; Fiona A J van den Heuvel; Martine A Collart; Rolf Boelens; H Th Marc Timmers
Journal:  EMBO J       Date:  2002-02-01       Impact factor: 11.598

3.  Yak1p, a DYRK family kinase, translocates to the nucleus and phosphorylates yeast Pop2p in response to a glucose signal.

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Journal:  Genes Dev       Date:  2001-05-15       Impact factor: 11.361

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Review 6.  The structural basis for deadenylation by the CCR4-NOT complex.

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Journal:  Protein Cell       Date:  2010-06-04       Impact factor: 14.870

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Journal:  RNA       Date:  2010-05-26       Impact factor: 4.942

8.  Crystal structure and functional properties of the human CCR4-CAF1 deadenylase complex.

Authors:  Ying Chen; Elena Khazina; Elisa Izaurralde; Oliver Weichenrieder
Journal:  Nucleic Acids Res       Date:  2021-06-21       Impact factor: 16.971

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10.  Comparative genomics of transcriptional control in the human malaria parasite Plasmodium falciparum.

Authors:  Richard M R Coulson; Neil Hall; Christos A Ouzounis
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