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Enhancer-driven alternative promoters of imprinted genes

In the current study, we characterized the expression and histone modification profiles of the alternative promoters found within imprinted Igf2r, Mest, Zac1, Peg3, Snrpn and non-imprinted Myc loci. In terms of expression pattern, the alternative promoters are highly tissue-specific, which is in a s...

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Detalles Bibliográficos
Autores principales: Kim, Joomyeong, Perera, Bambarendage P. U., Ghimire, Subash
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6267961/
https://www.ncbi.nlm.nih.gov/pubmed/30500864
http://dx.doi.org/10.1371/journal.pone.0208421
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author Kim, Joomyeong
Perera, Bambarendage P. U.
Ghimire, Subash
author_facet Kim, Joomyeong
Perera, Bambarendage P. U.
Ghimire, Subash
author_sort Kim, Joomyeong
collection PubMed
description In the current study, we characterized the expression and histone modification profiles of the alternative promoters found within imprinted Igf2r, Mest, Zac1, Peg3, Snrpn and non-imprinted Myc loci. In terms of expression pattern, the alternative promoters are highly tissue-specific, which is in a stark contrast to the ubiquitous expression of the corresponding main promoters. The alternative promoters are associated with the histone modification mark H3K4me1, but not with H3K4me3, which is frequently associated with the main promoters. Phylogenetic analyses also indicated that the majority of the alternative promoters are unique to the mammalian lineage, further suggesting the recent formation of these promoters during mammalian evolution. Overall, this study suggests that the alternative promoters of imprinted loci may have been derived from enhancers in recent evolutionary times and co-evolved with the genomic imprinting mechanism.
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spelling pubmed-62679612018-12-19 Enhancer-driven alternative promoters of imprinted genes Kim, Joomyeong Perera, Bambarendage P. U. Ghimire, Subash PLoS One Research Article In the current study, we characterized the expression and histone modification profiles of the alternative promoters found within imprinted Igf2r, Mest, Zac1, Peg3, Snrpn and non-imprinted Myc loci. In terms of expression pattern, the alternative promoters are highly tissue-specific, which is in a stark contrast to the ubiquitous expression of the corresponding main promoters. The alternative promoters are associated with the histone modification mark H3K4me1, but not with H3K4me3, which is frequently associated with the main promoters. Phylogenetic analyses also indicated that the majority of the alternative promoters are unique to the mammalian lineage, further suggesting the recent formation of these promoters during mammalian evolution. Overall, this study suggests that the alternative promoters of imprinted loci may have been derived from enhancers in recent evolutionary times and co-evolved with the genomic imprinting mechanism. Public Library of Science 2018-11-30 /pmc/articles/PMC6267961/ /pubmed/30500864 http://dx.doi.org/10.1371/journal.pone.0208421 Text en © 2018 Kim 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Kim, Joomyeong
Perera, Bambarendage P. U.
Ghimire, Subash
Enhancer-driven alternative promoters of imprinted genes
title Enhancer-driven alternative promoters of imprinted genes
title_full Enhancer-driven alternative promoters of imprinted genes
title_fullStr Enhancer-driven alternative promoters of imprinted genes
title_full_unstemmed Enhancer-driven alternative promoters of imprinted genes
title_short Enhancer-driven alternative promoters of imprinted genes
title_sort enhancer-driven alternative promoters of imprinted genes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6267961/
https://www.ncbi.nlm.nih.gov/pubmed/30500864
http://dx.doi.org/10.1371/journal.pone.0208421
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