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Integrative genomic analyses of promoter G-quadruplexes reveal their selective constraint and association with gene activation
G-quadruplexes (G4s) regulate DNA replication and gene transcription, and are enriched in promoters without fully appreciated functional relevance. Here we show high selection pressure on putative G4 (pG4) forming sequences in promoters through investigating genetic and genomic data. Analyses of 76,...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10257653/ https://www.ncbi.nlm.nih.gov/pubmed/37301913 http://dx.doi.org/10.1038/s42003-023-05015-6 |
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author | Li, Guangyue Su, Gongbo Wang, Yunxuan Wang, Wenmeng Shi, Jinming Li, Dangdang Sui, Guangchao |
author_facet | Li, Guangyue Su, Gongbo Wang, Yunxuan Wang, Wenmeng Shi, Jinming Li, Dangdang Sui, Guangchao |
author_sort | Li, Guangyue |
collection | PubMed |
description | G-quadruplexes (G4s) regulate DNA replication and gene transcription, and are enriched in promoters without fully appreciated functional relevance. Here we show high selection pressure on putative G4 (pG4) forming sequences in promoters through investigating genetic and genomic data. Analyses of 76,156 whole-genome sequences reveal that G-tracts and connecting loops in promoter pG4s display lower or higher allele frequencies, respectively, than pG4-flanking regions, and central guanines (Gs) in G-tracts show higher selection pressure than other Gs. Additionally, pG4-promoters produce over 72.4% of transcripts, and promoter G4-containing genes are expressed at relatively high levels. Most genes repressed by TMPyP4, a G4-ligand, regulate epigenetic processes, and promoter G4s are enriched with gene activation histone marks, chromatin remodeler and transcription factor binding sites. Consistently, cis-expression quantitative trait loci (cis-eQTLs) are enriched in promoter pG4s and their G-tracts. Overall, our study demonstrates selective constraint of promoter G4s and reinforces their stimulative role in gene expression. |
format | Online Article Text |
id | pubmed-10257653 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-102576532023-06-12 Integrative genomic analyses of promoter G-quadruplexes reveal their selective constraint and association with gene activation Li, Guangyue Su, Gongbo Wang, Yunxuan Wang, Wenmeng Shi, Jinming Li, Dangdang Sui, Guangchao Commun Biol Article G-quadruplexes (G4s) regulate DNA replication and gene transcription, and are enriched in promoters without fully appreciated functional relevance. Here we show high selection pressure on putative G4 (pG4) forming sequences in promoters through investigating genetic and genomic data. Analyses of 76,156 whole-genome sequences reveal that G-tracts and connecting loops in promoter pG4s display lower or higher allele frequencies, respectively, than pG4-flanking regions, and central guanines (Gs) in G-tracts show higher selection pressure than other Gs. Additionally, pG4-promoters produce over 72.4% of transcripts, and promoter G4-containing genes are expressed at relatively high levels. Most genes repressed by TMPyP4, a G4-ligand, regulate epigenetic processes, and promoter G4s are enriched with gene activation histone marks, chromatin remodeler and transcription factor binding sites. Consistently, cis-expression quantitative trait loci (cis-eQTLs) are enriched in promoter pG4s and their G-tracts. Overall, our study demonstrates selective constraint of promoter G4s and reinforces their stimulative role in gene expression. Nature Publishing Group UK 2023-06-10 /pmc/articles/PMC10257653/ /pubmed/37301913 http://dx.doi.org/10.1038/s42003-023-05015-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Li, Guangyue Su, Gongbo Wang, Yunxuan Wang, Wenmeng Shi, Jinming Li, Dangdang Sui, Guangchao Integrative genomic analyses of promoter G-quadruplexes reveal their selective constraint and association with gene activation |
title | Integrative genomic analyses of promoter G-quadruplexes reveal their selective constraint and association with gene activation |
title_full | Integrative genomic analyses of promoter G-quadruplexes reveal their selective constraint and association with gene activation |
title_fullStr | Integrative genomic analyses of promoter G-quadruplexes reveal their selective constraint and association with gene activation |
title_full_unstemmed | Integrative genomic analyses of promoter G-quadruplexes reveal their selective constraint and association with gene activation |
title_short | Integrative genomic analyses of promoter G-quadruplexes reveal their selective constraint and association with gene activation |
title_sort | integrative genomic analyses of promoter g-quadruplexes reveal their selective constraint and association with gene activation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10257653/ https://www.ncbi.nlm.nih.gov/pubmed/37301913 http://dx.doi.org/10.1038/s42003-023-05015-6 |
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