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The NOT Proteins Are Part of the CCR4 Transcriptional Complex and Affect Gene Expression Both Positively and Negatively

Overview
Journal EMBO J
Date 1998 Mar 28
PMID 9463387
Citations 101
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Abstract

The CCR4 transcriptional regulatory complex consisting of CCR4, CAF1, DBF2 and other unidentified factors is one of several groups of proteins that affect gene expression. Using mass spectrometry, we have identified the 195, 185 and 116 kDa species which are part of the CCR4 complex. The 195 and 185 kDa proteins were found to be NOT1 and the 116 kDa species was identical to NOT3. NOT1, 2, 3 and 4 proteins are part of a regulatory complex that negatively affects transcription. All four NOT proteins were found to co-immunoprecipitate with CCR4 and CAF1, and NOT1 co-purified with CCR4 and CAF1 through three chromatographic steps in a complex estimated to be 1.2x10(6) Da in size. Mutations in the NOT genes affected many of the same genes and processes that are affected by defects in the CCR4 complex components, including reduction in ADH2 derepression, defective cell wall integrity and increased sensitivity to monoand divalent ions. Similarly, ccr4, caf1 and dbf2 alleles negatively regulated FUS1-lacZ expression, as do defects in the NOT genes. These results indicate that the NOT proteins are physically and functionally part of the CCR4 complex which forms a unique and novel complex that affects transcription both positively and negatively.

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References
1.
Draper M, Liu H, Nelsbach A, Mosley S, Denis C . CCR4 is a glucose-regulated transcription factor whose leucine-rich repeat binds several proteins important for placing CCR4 in its proper promoter context. Mol Cell Biol. 1994; 14(7):4522-31. PMC: 358824. DOI: 10.1128/mcb.14.7.4522-4531.1994. View

2.
Lamond A, Mann M . Cell biology and the genome projects a concerted strategy for characterizing multiprotein complexes by using mass spectrometry. Trends Cell Biol. 1997; 7(4):139-42. DOI: 10.1016/S0962-8924(97)01031-3. View

3.
Mann M, Wilm M . Error-tolerant identification of peptides in sequence databases by peptide sequence tags. Anal Chem. 1994; 66(24):4390-9. DOI: 10.1021/ac00096a002. View

4.
Wade P, Werel W, Fentzke R, Thompson N, Leykam J, Burgess R . A novel collection of accessory factors associated with yeast RNA polymerase II. Protein Expr Purif. 1996; 8(1):85-90. DOI: 10.1006/prep.1996.0077. View

5.
Wilm M, Shevchenko A, Houthaeve T, Breit S, Schweigerer L, Fotsis T . Femtomole sequencing of proteins from polyacrylamide gels by nano-electrospray mass spectrometry. Nature. 1996; 379(6564):466-9. DOI: 10.1038/379466a0. View