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The dual control of TFIIB recruitment by NC2 is gene specific
Negative co-factor 2 (NC2) is a conserved eukaryotic complex composed of two subunits, NC2α (Drap1) and NC2β (Dr1) that associate through a histone-fold motif. In this work, we generated mutants of NC2, characterized target genes for these mutants and studied the assembly of NC2 and general transcri...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2241854/ https://www.ncbi.nlm.nih.gov/pubmed/18048413 http://dx.doi.org/10.1093/nar/gkm1078 |
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author | Masson, Patrick Leimgruber, Elisa Creton, Sandrine Collart, Martine A. |
author_facet | Masson, Patrick Leimgruber, Elisa Creton, Sandrine Collart, Martine A. |
author_sort | Masson, Patrick |
collection | PubMed |
description | Negative co-factor 2 (NC2) is a conserved eukaryotic complex composed of two subunits, NC2α (Drap1) and NC2β (Dr1) that associate through a histone-fold motif. In this work, we generated mutants of NC2, characterized target genes for these mutants and studied the assembly of NC2 and general transcription factors on target promoters. We determined that the two NC2 subunits mostly function together to be recruited to DNA and regulate gene expression. We found that NC2 strongly controls promoter association of TFIIB, both negatively and positively. We could attribute the gene-specific repressor effect of NC2 on TFIIB to the C-terminal domain of NC2β, and define that it requires ORF sequences of the target gene. In contrast, the positive function of NC2 on TFIIB targets is more general and requires adequate levels of the NC2 histone-fold heterodimer on promoters. Finally, we determined that NC2 becomes limiting for TATA-binding protein (TBP) association with a heat inducible promoter under heat stress. This study demonstrates an important positive role of NC2 for formation of the pre-initiation complex on promoters, under normal conditions through control of TFIIB, or upon activation by stress via control of TBP. |
format | Text |
id | pubmed-2241854 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-22418542008-02-21 The dual control of TFIIB recruitment by NC2 is gene specific Masson, Patrick Leimgruber, Elisa Creton, Sandrine Collart, Martine A. Nucleic Acids Res Molecular Biology Negative co-factor 2 (NC2) is a conserved eukaryotic complex composed of two subunits, NC2α (Drap1) and NC2β (Dr1) that associate through a histone-fold motif. In this work, we generated mutants of NC2, characterized target genes for these mutants and studied the assembly of NC2 and general transcription factors on target promoters. We determined that the two NC2 subunits mostly function together to be recruited to DNA and regulate gene expression. We found that NC2 strongly controls promoter association of TFIIB, both negatively and positively. We could attribute the gene-specific repressor effect of NC2 on TFIIB to the C-terminal domain of NC2β, and define that it requires ORF sequences of the target gene. In contrast, the positive function of NC2 on TFIIB targets is more general and requires adequate levels of the NC2 histone-fold heterodimer on promoters. Finally, we determined that NC2 becomes limiting for TATA-binding protein (TBP) association with a heat inducible promoter under heat stress. This study demonstrates an important positive role of NC2 for formation of the pre-initiation complex on promoters, under normal conditions through control of TFIIB, or upon activation by stress via control of TBP. Oxford University Press 2008-02 2007-11-29 /pmc/articles/PMC2241854/ /pubmed/18048413 http://dx.doi.org/10.1093/nar/gkm1078 Text en © 2007 The Author(s) http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Molecular Biology Masson, Patrick Leimgruber, Elisa Creton, Sandrine Collart, Martine A. The dual control of TFIIB recruitment by NC2 is gene specific |
title | The dual control of TFIIB recruitment by NC2 is gene specific |
title_full | The dual control of TFIIB recruitment by NC2 is gene specific |
title_fullStr | The dual control of TFIIB recruitment by NC2 is gene specific |
title_full_unstemmed | The dual control of TFIIB recruitment by NC2 is gene specific |
title_short | The dual control of TFIIB recruitment by NC2 is gene specific |
title_sort | dual control of tfiib recruitment by nc2 is gene specific |
topic | Molecular Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2241854/ https://www.ncbi.nlm.nih.gov/pubmed/18048413 http://dx.doi.org/10.1093/nar/gkm1078 |
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