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Structural Basis of Transcriptional Gene Silencing Mediated by Arabidopsis MOM1
Shifts between epigenetic states of transcriptional activity are typically correlated with changes in epigenetic marks. However, exceptions to this rule suggest the existence of additional, as yet uncharacterized, layers of epigenetic regulation. MOM1, a protein of 2,001 amino acids that acts as a t...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3276543/ https://www.ncbi.nlm.nih.gov/pubmed/22346760 http://dx.doi.org/10.1371/journal.pgen.1002484 |
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author | Nishimura, Taisuke Molinard, Guillaume Petty, Tom J. Broger, Larissa Gabus, Caroline Halazonetis, Thanos D. Thore, Stéphane Paszkowski, Jerzy |
author_facet | Nishimura, Taisuke Molinard, Guillaume Petty, Tom J. Broger, Larissa Gabus, Caroline Halazonetis, Thanos D. Thore, Stéphane Paszkowski, Jerzy |
author_sort | Nishimura, Taisuke |
collection | PubMed |
description | Shifts between epigenetic states of transcriptional activity are typically correlated with changes in epigenetic marks. However, exceptions to this rule suggest the existence of additional, as yet uncharacterized, layers of epigenetic regulation. MOM1, a protein of 2,001 amino acids that acts as a transcriptional silencer, represents such an exception. Here we define the 82 amino acid domain called CMM2 (Conserved MOM1 Motif 2) as a minimal MOM1 fragment capable of transcriptional regulation. As determined by X-ray crystallography, this motif folds into an unusual hendecad-based coiled-coil. Structure-based mutagenesis followed by transgenic complementation tests in plants demonstrate that CMM2 and its dimerization are effective for transcriptional suppression at chromosomal loci co-regulated by MOM1 and the siRNA pathway but not at loci controlled by MOM1 in an siRNA–independent fashion. These results reveal a surprising separation of epigenetic activities that enable the single, large MOM1 protein to coordinate cooperating mechanisms of epigenetic regulation. |
format | Online Article Text |
id | pubmed-3276543 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-32765432012-02-15 Structural Basis of Transcriptional Gene Silencing Mediated by Arabidopsis MOM1 Nishimura, Taisuke Molinard, Guillaume Petty, Tom J. Broger, Larissa Gabus, Caroline Halazonetis, Thanos D. Thore, Stéphane Paszkowski, Jerzy PLoS Genet Research Article Shifts between epigenetic states of transcriptional activity are typically correlated with changes in epigenetic marks. However, exceptions to this rule suggest the existence of additional, as yet uncharacterized, layers of epigenetic regulation. MOM1, a protein of 2,001 amino acids that acts as a transcriptional silencer, represents such an exception. Here we define the 82 amino acid domain called CMM2 (Conserved MOM1 Motif 2) as a minimal MOM1 fragment capable of transcriptional regulation. As determined by X-ray crystallography, this motif folds into an unusual hendecad-based coiled-coil. Structure-based mutagenesis followed by transgenic complementation tests in plants demonstrate that CMM2 and its dimerization are effective for transcriptional suppression at chromosomal loci co-regulated by MOM1 and the siRNA pathway but not at loci controlled by MOM1 in an siRNA–independent fashion. These results reveal a surprising separation of epigenetic activities that enable the single, large MOM1 protein to coordinate cooperating mechanisms of epigenetic regulation. Public Library of Science 2012-02-09 /pmc/articles/PMC3276543/ /pubmed/22346760 http://dx.doi.org/10.1371/journal.pgen.1002484 Text en Nishimura et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Nishimura, Taisuke Molinard, Guillaume Petty, Tom J. Broger, Larissa Gabus, Caroline Halazonetis, Thanos D. Thore, Stéphane Paszkowski, Jerzy Structural Basis of Transcriptional Gene Silencing Mediated by Arabidopsis MOM1 |
title | Structural Basis of Transcriptional Gene Silencing Mediated by Arabidopsis MOM1 |
title_full | Structural Basis of Transcriptional Gene Silencing Mediated by Arabidopsis MOM1 |
title_fullStr | Structural Basis of Transcriptional Gene Silencing Mediated by Arabidopsis MOM1 |
title_full_unstemmed | Structural Basis of Transcriptional Gene Silencing Mediated by Arabidopsis MOM1 |
title_short | Structural Basis of Transcriptional Gene Silencing Mediated by Arabidopsis MOM1 |
title_sort | structural basis of transcriptional gene silencing mediated by arabidopsis mom1 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3276543/ https://www.ncbi.nlm.nih.gov/pubmed/22346760 http://dx.doi.org/10.1371/journal.pgen.1002484 |
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