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Study on the spatial distribution patterns of histone modifications in Hippo pathway genes
Hippo pathway can regulate cell division, differentiation and apoptosis, and control the shape and size of organs. To study the distribution patterns of histone modifications of Hippo pathway genes in embryonic stem cells is helpful to understand the molecular regulation mechanism of histone modific...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Biophysics Reports Editorial Office
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10240540/ https://www.ncbi.nlm.nih.gov/pubmed/37288084 http://dx.doi.org/10.52601/bpr.2021.200042 |
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author | Su, Wenxia Zhang, Dimeng Zhang, Qiang Li, Qianzhong |
author_facet | Su, Wenxia Zhang, Dimeng Zhang, Qiang Li, Qianzhong |
author_sort | Su, Wenxia |
collection | PubMed |
description | Hippo pathway can regulate cell division, differentiation and apoptosis, and control the shape and size of organs. To study the distribution patterns of histone modifications of Hippo pathway genes in embryonic stem cells is helpful to understand the molecular regulation mechanism of histone modification and Hippo pathway on stem cell self-renewal. In this study, 19 genes of Hippo pathway including YAP, TAZ, LATS1/2, MST1 and SAV1, and eight histone modifications in embryonic stem cells were chosen to study the spatial distribution patterns of histone modifications. It was found that there were obvious type specificity and the location preference of target regions in the distributions of histone modifications, and H3K4me3 and H3K36me3 played the most important regulatory roles. Through the correlation analysis of histone modifications, a histone modification functional cluster composed of H3K4ac, H3K4me3, H3K9ac and H3K27ac was detected in YAP. In addition, the spatial distribution patterns of histone modifications in Hippo pathway genes were obtained, which provided a new theoretical reference for elucidating the mechanism of histone modifications regulating the gene expression of Hippo pathway, and for revealing the molecular regulatory mechanism of histone modifications affecting the self-renewal of embryonic stem cells by regulating the Hippo pathway. |
format | Online Article Text |
id | pubmed-10240540 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Biophysics Reports Editorial Office |
record_format | MEDLINE/PubMed |
spelling | pubmed-102405402023-06-07 Study on the spatial distribution patterns of histone modifications in Hippo pathway genes Su, Wenxia Zhang, Dimeng Zhang, Qiang Li, Qianzhong Biophys Rep Research Article Hippo pathway can regulate cell division, differentiation and apoptosis, and control the shape and size of organs. To study the distribution patterns of histone modifications of Hippo pathway genes in embryonic stem cells is helpful to understand the molecular regulation mechanism of histone modification and Hippo pathway on stem cell self-renewal. In this study, 19 genes of Hippo pathway including YAP, TAZ, LATS1/2, MST1 and SAV1, and eight histone modifications in embryonic stem cells were chosen to study the spatial distribution patterns of histone modifications. It was found that there were obvious type specificity and the location preference of target regions in the distributions of histone modifications, and H3K4me3 and H3K36me3 played the most important regulatory roles. Through the correlation analysis of histone modifications, a histone modification functional cluster composed of H3K4ac, H3K4me3, H3K9ac and H3K27ac was detected in YAP. In addition, the spatial distribution patterns of histone modifications in Hippo pathway genes were obtained, which provided a new theoretical reference for elucidating the mechanism of histone modifications regulating the gene expression of Hippo pathway, and for revealing the molecular regulatory mechanism of histone modifications affecting the self-renewal of embryonic stem cells by regulating the Hippo pathway. Biophysics Reports Editorial Office 2021-02-28 /pmc/articles/PMC10240540/ /pubmed/37288084 http://dx.doi.org/10.52601/bpr.2021.200042 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Su, Wenxia Zhang, Dimeng Zhang, Qiang Li, Qianzhong Study on the spatial distribution patterns of histone modifications in Hippo pathway genes |
title | Study on the spatial distribution patterns of histone modifications in Hippo pathway genes |
title_full | Study on the spatial distribution patterns of histone modifications in Hippo pathway genes |
title_fullStr | Study on the spatial distribution patterns of histone modifications in Hippo pathway genes |
title_full_unstemmed | Study on the spatial distribution patterns of histone modifications in Hippo pathway genes |
title_short | Study on the spatial distribution patterns of histone modifications in Hippo pathway genes |
title_sort | study on the spatial distribution patterns of histone modifications in hippo pathway genes |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10240540/ https://www.ncbi.nlm.nih.gov/pubmed/37288084 http://dx.doi.org/10.52601/bpr.2021.200042 |
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