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Genome-wide analysis of DNA G-quadruplex motifs across 37 species provides insights into G4 evolution
G-quadruplex (G4) structures have been predicted in the genomes of many organisms and proven to play regulatory roles in diverse cellular activities. However, there is little information on the evolutionary history and distribution characteristics of G4s. Here, whole-genome characteristics of potent...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7822830/ https://www.ncbi.nlm.nih.gov/pubmed/33483610 http://dx.doi.org/10.1038/s42003-020-01643-4 |
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author | Wu, Feng Niu, Kangkang Cui, Yong Li, Cencen Lyu, Mo Ren, Yandong Chen, Yanfei Deng, Huimin Huang, Lihua Zheng, Sichun Liu, Lin Wang, Jian Song, Qisheng Xiang, Hui Feng, Qili |
author_facet | Wu, Feng Niu, Kangkang Cui, Yong Li, Cencen Lyu, Mo Ren, Yandong Chen, Yanfei Deng, Huimin Huang, Lihua Zheng, Sichun Liu, Lin Wang, Jian Song, Qisheng Xiang, Hui Feng, Qili |
author_sort | Wu, Feng |
collection | PubMed |
description | G-quadruplex (G4) structures have been predicted in the genomes of many organisms and proven to play regulatory roles in diverse cellular activities. However, there is little information on the evolutionary history and distribution characteristics of G4s. Here, whole-genome characteristics of potential G4s were studied in 37 evolutionarily representative species. During evolution, the number, length, and density of G4s generally increased. Immunofluorescence in seven species confirmed G4s’ presence and evolutionary pattern. G4s tended to cluster in chromosomes and were enriched in genetic regions. Short-loop G4s were conserved in most species, while loop-length diversity also existed, especially in mammals. The proportion of G4-bearing genes and orthologue genes, which appeared to be increasingly enriched in transcription factors, gradually increased. The antagonistic relationship between G4s and DNA methylation sites was detected. These findings imply that organisms may have evolutionarily developed G4 into a novel reversible and elaborate transcriptional regulatory mechanism benefiting multiple physiological activities of higher organisms. |
format | Online Article Text |
id | pubmed-7822830 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78228302021-01-29 Genome-wide analysis of DNA G-quadruplex motifs across 37 species provides insights into G4 evolution Wu, Feng Niu, Kangkang Cui, Yong Li, Cencen Lyu, Mo Ren, Yandong Chen, Yanfei Deng, Huimin Huang, Lihua Zheng, Sichun Liu, Lin Wang, Jian Song, Qisheng Xiang, Hui Feng, Qili Commun Biol Article G-quadruplex (G4) structures have been predicted in the genomes of many organisms and proven to play regulatory roles in diverse cellular activities. However, there is little information on the evolutionary history and distribution characteristics of G4s. Here, whole-genome characteristics of potential G4s were studied in 37 evolutionarily representative species. During evolution, the number, length, and density of G4s generally increased. Immunofluorescence in seven species confirmed G4s’ presence and evolutionary pattern. G4s tended to cluster in chromosomes and were enriched in genetic regions. Short-loop G4s were conserved in most species, while loop-length diversity also existed, especially in mammals. The proportion of G4-bearing genes and orthologue genes, which appeared to be increasingly enriched in transcription factors, gradually increased. The antagonistic relationship between G4s and DNA methylation sites was detected. These findings imply that organisms may have evolutionarily developed G4 into a novel reversible and elaborate transcriptional regulatory mechanism benefiting multiple physiological activities of higher organisms. Nature Publishing Group UK 2021-01-22 /pmc/articles/PMC7822830/ /pubmed/33483610 http://dx.doi.org/10.1038/s42003-020-01643-4 Text en © The Author(s) 2021 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/. |
spellingShingle | Article Wu, Feng Niu, Kangkang Cui, Yong Li, Cencen Lyu, Mo Ren, Yandong Chen, Yanfei Deng, Huimin Huang, Lihua Zheng, Sichun Liu, Lin Wang, Jian Song, Qisheng Xiang, Hui Feng, Qili Genome-wide analysis of DNA G-quadruplex motifs across 37 species provides insights into G4 evolution |
title | Genome-wide analysis of DNA G-quadruplex motifs across 37 species provides insights into G4 evolution |
title_full | Genome-wide analysis of DNA G-quadruplex motifs across 37 species provides insights into G4 evolution |
title_fullStr | Genome-wide analysis of DNA G-quadruplex motifs across 37 species provides insights into G4 evolution |
title_full_unstemmed | Genome-wide analysis of DNA G-quadruplex motifs across 37 species provides insights into G4 evolution |
title_short | Genome-wide analysis of DNA G-quadruplex motifs across 37 species provides insights into G4 evolution |
title_sort | genome-wide analysis of dna g-quadruplex motifs across 37 species provides insights into g4 evolution |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7822830/ https://www.ncbi.nlm.nih.gov/pubmed/33483610 http://dx.doi.org/10.1038/s42003-020-01643-4 |
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