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Transcription factor binding to Caenorhabditis elegans first introns reveals lack of redundancy with gene promoters
Gene expression is controlled through the binding of transcription factors (TFs) to regulatory genomic regions. First introns are longer than other introns in multiple eukaryotic species and are under selective constraint. Here we explore the importance of first introns in TF binding in the nematode...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3874175/ https://www.ncbi.nlm.nih.gov/pubmed/24068555 http://dx.doi.org/10.1093/nar/gkt858 |
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author | Fuxman Bass, Juan I. Tamburino, Alex M. Mori, Akihiro Beittel, Nathan Weirauch, Matthew T. Reece-Hoyes, John S. Walhout, Albertha J. M. |
author_facet | Fuxman Bass, Juan I. Tamburino, Alex M. Mori, Akihiro Beittel, Nathan Weirauch, Matthew T. Reece-Hoyes, John S. Walhout, Albertha J. M. |
author_sort | Fuxman Bass, Juan I. |
collection | PubMed |
description | Gene expression is controlled through the binding of transcription factors (TFs) to regulatory genomic regions. First introns are longer than other introns in multiple eukaryotic species and are under selective constraint. Here we explore the importance of first introns in TF binding in the nematode Caenorhabditis elegans by combining computational predictions and experimentally derived TF–DNA interaction data. We found that first introns of C. elegans genes, particularly those for families enriched in long first introns, are more conserved in length, have more conserved predicted TF interactions and are bound by more TFs than other introns. We detected a significant positive correlation between first intron size and the number of TF interactions obtained from chromatin immunoprecipitation assays or determined by yeast one-hybrid assays. TFs that bind first introns are largely different from those binding promoters, suggesting that the different interactions are complementary rather than redundant. By combining first intron and promoter interactions, we found that genes that share a large fraction of TF interactions are more likely to be co-expressed than when only TF interactions with promoters are considered. Altogether, our data suggest that C. elegans gene regulation may be additive through the combined effects of multiple regulatory regions. |
format | Online Article Text |
id | pubmed-3874175 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-38741752013-12-28 Transcription factor binding to Caenorhabditis elegans first introns reveals lack of redundancy with gene promoters Fuxman Bass, Juan I. Tamburino, Alex M. Mori, Akihiro Beittel, Nathan Weirauch, Matthew T. Reece-Hoyes, John S. Walhout, Albertha J. M. Nucleic Acids Res Gene Regulation, Chromatin and Epigenetics Gene expression is controlled through the binding of transcription factors (TFs) to regulatory genomic regions. First introns are longer than other introns in multiple eukaryotic species and are under selective constraint. Here we explore the importance of first introns in TF binding in the nematode Caenorhabditis elegans by combining computational predictions and experimentally derived TF–DNA interaction data. We found that first introns of C. elegans genes, particularly those for families enriched in long first introns, are more conserved in length, have more conserved predicted TF interactions and are bound by more TFs than other introns. We detected a significant positive correlation between first intron size and the number of TF interactions obtained from chromatin immunoprecipitation assays or determined by yeast one-hybrid assays. TFs that bind first introns are largely different from those binding promoters, suggesting that the different interactions are complementary rather than redundant. By combining first intron and promoter interactions, we found that genes that share a large fraction of TF interactions are more likely to be co-expressed than when only TF interactions with promoters are considered. Altogether, our data suggest that C. elegans gene regulation may be additive through the combined effects of multiple regulatory regions. Oxford University Press 2014-01-01 2013-09-24 /pmc/articles/PMC3874175/ /pubmed/24068555 http://dx.doi.org/10.1093/nar/gkt858 Text en © The Author(s) 2013. Published by Oxford University Press. http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by/3.0/), which permits non-commercial reuse, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Gene Regulation, Chromatin and Epigenetics Fuxman Bass, Juan I. Tamburino, Alex M. Mori, Akihiro Beittel, Nathan Weirauch, Matthew T. Reece-Hoyes, John S. Walhout, Albertha J. M. Transcription factor binding to Caenorhabditis elegans first introns reveals lack of redundancy with gene promoters |
title | Transcription factor binding to Caenorhabditis elegans first introns reveals lack of redundancy with gene promoters |
title_full | Transcription factor binding to Caenorhabditis elegans first introns reveals lack of redundancy with gene promoters |
title_fullStr | Transcription factor binding to Caenorhabditis elegans first introns reveals lack of redundancy with gene promoters |
title_full_unstemmed | Transcription factor binding to Caenorhabditis elegans first introns reveals lack of redundancy with gene promoters |
title_short | Transcription factor binding to Caenorhabditis elegans first introns reveals lack of redundancy with gene promoters |
title_sort | transcription factor binding to caenorhabditis elegans first introns reveals lack of redundancy with gene promoters |
topic | Gene Regulation, Chromatin and Epigenetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3874175/ https://www.ncbi.nlm.nih.gov/pubmed/24068555 http://dx.doi.org/10.1093/nar/gkt858 |
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