Role of the C-terminal Binding Protein Pxdls Motif Binding Cleft in Protein Interactions and Transcriptional Repression.
From: School of Molecular and Microbial Biosciences, University of Sydney, Sydney, New South Wales 2006, Australia.
Molecular and cellular biology
- Publish Date: Nov 2006
- ISSN: 0270-7306
- Volume: 26
- Issue: 21
- Pages: 8202-13
- Medium: Print
- Language: English
- Citation (JAMA): Quinlan Kate G R, Verger Alexis, Kwok Alister, et al. Role of the C-terminal Binding Protein Pxdls Motif Binding Cleft in Protein Interactions and Transcriptional Repression.. Mol. Cell. Biol. Nov 2006;26:8202-13
Abstract
C-terminal binding proteins (CtBPs) are multifunctional proteins that can mediate gene repression. CtBPs contain a cleft that binds Pro-X-Asp-Leu-Ser (PXDLS) motifs. PXDLS motifs occur in numerous transcription factors and in effectors of gene repression, such as certain histone deacetylases. CtBPs have been depicted as bridging proteins that self-associate and link PXDLS-containing transcription factors to PXDLS-containing chromatin-modifying enzymes. CtBPs also recruit effectors that do not contain recognizable PXDLS motifs. We have investigated the importance of the PXDLS binding cleft to CtBP’s interactions with various partner proteins and to its ability to repress transcription. We used CtBP cleft mutant and cleft-filled fusion derivatives to distinguish between partner proteins that bind in the cleft and elsewhere on the CtBP surface. Functional assays demonstrate that CtBP mutants that carry defective clefts retain repression activity when fused to heterologous DNA-binding domains. This result suggests that the cleft is not essential for recruiting effectors. In contrast, when tested in the absence of a fused DNA-binding domain, disruption of the cleft abrogates repression activity. These results demonstrate that the PXDLS binding cleft is functionally important but suggest that it is primarily required for localization of the CtBP complex to promoter-bound transcription factors.
Mesh Headings (Keywords): Amino Acid Sequence, Animals, Binding Sites, DNA-Binding Proteins, Gene Expression Regulation, Mice, Molecular Sequence Data, NIH 3T3 Cells, Phosphoproteins, Protein Binding, Protein Conformation, Recombinant Fusion Proteins, Transcription, Genetic, Two-Hybrid System Techniques
Check for Full Text / PubMed Unique Identifier (PMID): 16940173
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