ArticleBMC genomics2009
Cross-species mapping of bidirectional promoters enables prediction of unannotated 5' UTRs and identification of species-specific transcripts.
Article in BMC genomics, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.
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Who cites it
15 citing papers in PubMed, 45 citations in OpenAlex.
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- Genetic variability of the activity of bidirectional promoters: a pilot study in bovine muscle.DNA research : an international journal for rapid publication of reports on genes and genomes · 2017Article
- Volatile evolution of long noncoding RNA repertoires: mechanisms and biological implications.Trends in genetics : TIG · 2014Review
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- RhesusBase: a knowledgebase for the monkey research community.Nucleic acids research · 2013Article
- Identification of regulatory regions of bidirectional genes in cervical cancer.BMC medical genomics · 2013Article
- Bidirectional promoters as important drivers for the emergence of species-specific transcripts.PloS one · 2013Article
- NF-κB activity in perinatal brain during infectious and hypoxic-ischemic insults revealed by a reporter mouse.Brain pathology (Zurich, Switzerland) · 2012Article
- CNS effects of CB2 cannabinoid receptors: beyond neuro-immuno-cannabinoid activity.Journal of psychopharmacology (Oxford, England) · 2012Review
- Efficient expression from one CMV enhancer controlling two core promoters.Molecular biotechnology · 2011Article
- Genome-wide analysis of the transcription factor binding preference of human bi-directional promoters and functional annotation of related gene pairs.BMC systems biology · 2011Article
- Mouse Dfa is a repressor of TATA-box promoters and interacts with the Abt1 activator of basal transcription.The Journal of biological chemistry · 2010Article
- Analysis of gene order conservation in eukaryotes identifies transcriptionally and functionally linked genes.PloS one · 2010Article
- Review
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Authors and funding
6 authors at 4 institutions in 1 country.
Funding
Abstract
backgroundBidirectional promoters are shared regulatory regions that influence the expression of two oppositely oriented genes. This type of regulatory architecture is found more frequently than expected by chance in the human genome, yet many specifics underlying the regulatory design are unknown. Given that the function of most orthologous genes is similar across species, we hypothesized that the architecture and regulation of bidirectional promoters might also be similar across species, representing a core regulatory structure and enabling annotation of these regions in additional mammalian genomes.
resultsBy mapping the intergenic distances of genes in human, chimpanzee, bovine, murine, and rat, we show an enrichment for pairs of genes equal to or less than 1,000 bp between their adjacent 5' ends ("head-to-head") compared to pairs of genes that fall in the same orientation ("head-to-tail") or whose 3' ends are side-by-side ("tail-to-tail"). A representative set of 1,369 human bidirectional promoters was mapped to orthologous sequences in other mammals. We confirmed predictions for 5' UTRs in nine of ten manual picks in bovine based on comparison to the orthologous human promoter set and in six of seven predictions in human based on comparison to the bovine dataset. The two predictions that did not have orthology as bidirectional promoters in the other species resulted from unique events that initiated transcription in the opposite direction in only those species. We found evidence supporting the independent emergence of bidirectional promoters from the family of five RecQ helicase genes, which gained their bidirectional promoters and partner genes independently rather than through a duplication process. Furthermore, by expanding our comparisons from pairwise to multispecies analyses we developed a map representing a core set of bidirectional promoters in mammals.
conclusionWe show that the orthologous positions of bidirectional promoters provide a reliable guide to directly annotate over one thousand regulatory regions in sequences of mammalian genomes, while also serving as a useful tool to predict 5' UTR positions and identify genes that are novel to a single species.
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.