Transcription factor binding to Caenorhabditis elegans first introns reveals lack of redundancy with gene promoters
Authors
Fuxman Bass, Juan I.Tamburino, Alex M.
Mori, Akihiro
Beittel, Nathan
Weirauch, Matthew T.
Reece-Hoyes, John S.
Walhout, Albertha J. M.
Document Type
Journal ArticlePublication Date
2014-01-07Keywords
Gene RegulationChromatin
Epigenetics
Cell Biology
Computational Biology
Molecular Genetics
Systems Biology
Metadata
Show full item recordAbstract
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.Source
Fuxman Bass JI, Tamburino AM, Mori A, Beittel N, Weirauch MT, Reece-Hoyes JS, Walhout AJ. Transcription factor binding to Caenorhabditis elegans first introns reveals lack of redundancy with gene promoters. Nucleic Acids Res. 2014 Jan 7;42(1):153-62. doi: 10.1093/nar/gkt858. Link to article on publisher's siteDOI
10.1093/nar/gkt858Permanent Link to this Item
http://hdl.handle.net/20.500.14038/49915PubMed ID
24068555Related Resources
Link to Article in PubMedRights
Copyright The Author(s) 2013. Published by Oxford University Press. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
ae974a485f413a2113503eed53cd6c53
10.1093/nar/gkt858
