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Transcription factor binding to Caenorhabditis elegans first introns reveals lack of redundancy with gene promoters
- Source :
- Nucleic Acids Research
- Publication Year :
- 2013
- Publisher :
- Oxford University Press (OUP), 2013.
-
Abstract
- 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.
- Subjects :
- Regulation of gene expression
Genetics
Intron
Promoter
Gene Regulation, Chromatin and Epigenetics
Biology
biology.organism_classification
Introns
Gene Expression Regulation
Regulatory sequence
Multigene Family
Animals
Gene Regulatory Networks
Caenorhabditis elegans
Promoter Regions, Genetic
Gene
Transcription factor
Chromatin immunoprecipitation
Transcription Factors
Subjects
Details
- ISSN :
- 13624962 and 03051048
- Volume :
- 42
- Database :
- OpenAIRE
- Journal :
- Nucleic Acids Research
- Accession number :
- edsair.doi.dedup.....70b251f2ffa9b2a703b68a769ce1490b
- Full Text :
- https://doi.org/10.1093/nar/gkt858