Cargando…
Stella Regulates the Development of Female Germline Stem Cells by Modulating Chromatin Structure and DNA Methylation
Female germline stem cells (FGSCs) have the ability to self-renew and differentiate into oocytes. Stella, encoded by a maternal effect gene, plays an important role in oogenesis and early embryonic development. However, its function in FGSCs remains unclear. In this study, we showed that CRISPR/Cas9...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9066111/ https://www.ncbi.nlm.nih.gov/pubmed/35541912 http://dx.doi.org/10.7150/ijbs.69240 |
_version_ | 1784699735319248896 |
---|---|
author | Hou, Changliang Zhao, Xinyan Tian, Geng G. Wu, Ji |
author_facet | Hou, Changliang Zhao, Xinyan Tian, Geng G. Wu, Ji |
author_sort | Hou, Changliang |
collection | PubMed |
description | Female germline stem cells (FGSCs) have the ability to self-renew and differentiate into oocytes. Stella, encoded by a maternal effect gene, plays an important role in oogenesis and early embryonic development. However, its function in FGSCs remains unclear. In this study, we showed that CRISPR/Cas9-mediated knockout of Stella promoted FGSC proliferation and reduced the level of genome-wide DNA methylation of FGSCs. Conversely, Stella overexpression led to the opposite results, and enhanced FGSC differentiation. We also performed an integrative analysis of chromatin immunoprecipitation followed by high-throughput sequencing (ChIP-seq), high-throughput genome-wide chromosome conformation capture (Hi-C), and use of our published epigenetic data. Results indicated that the binding sites of STELLA and active histones H3K4me3 and H3K27ac were enriched near the TAD boundaries. Hi-C analysis showed that Stella overexpression attenuated the interaction within TADs, and interestingly enhanced the TAD boundary strength in STELLA-associated regions. Taking these findings together, our study not only reveals the role of Stella in regulating DNA methylation and chromatin structure, but also provides a better understanding of FGSC development. |
format | Online Article Text |
id | pubmed-9066111 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-90661112022-05-09 Stella Regulates the Development of Female Germline Stem Cells by Modulating Chromatin Structure and DNA Methylation Hou, Changliang Zhao, Xinyan Tian, Geng G. Wu, Ji Int J Biol Sci Research Paper Female germline stem cells (FGSCs) have the ability to self-renew and differentiate into oocytes. Stella, encoded by a maternal effect gene, plays an important role in oogenesis and early embryonic development. However, its function in FGSCs remains unclear. In this study, we showed that CRISPR/Cas9-mediated knockout of Stella promoted FGSC proliferation and reduced the level of genome-wide DNA methylation of FGSCs. Conversely, Stella overexpression led to the opposite results, and enhanced FGSC differentiation. We also performed an integrative analysis of chromatin immunoprecipitation followed by high-throughput sequencing (ChIP-seq), high-throughput genome-wide chromosome conformation capture (Hi-C), and use of our published epigenetic data. Results indicated that the binding sites of STELLA and active histones H3K4me3 and H3K27ac were enriched near the TAD boundaries. Hi-C analysis showed that Stella overexpression attenuated the interaction within TADs, and interestingly enhanced the TAD boundary strength in STELLA-associated regions. Taking these findings together, our study not only reveals the role of Stella in regulating DNA methylation and chromatin structure, but also provides a better understanding of FGSC development. Ivyspring International Publisher 2022-04-18 /pmc/articles/PMC9066111/ /pubmed/35541912 http://dx.doi.org/10.7150/ijbs.69240 Text en © The author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions. |
spellingShingle | Research Paper Hou, Changliang Zhao, Xinyan Tian, Geng G. Wu, Ji Stella Regulates the Development of Female Germline Stem Cells by Modulating Chromatin Structure and DNA Methylation |
title | Stella Regulates the Development of Female Germline Stem Cells by Modulating Chromatin Structure and DNA Methylation |
title_full | Stella Regulates the Development of Female Germline Stem Cells by Modulating Chromatin Structure and DNA Methylation |
title_fullStr | Stella Regulates the Development of Female Germline Stem Cells by Modulating Chromatin Structure and DNA Methylation |
title_full_unstemmed | Stella Regulates the Development of Female Germline Stem Cells by Modulating Chromatin Structure and DNA Methylation |
title_short | Stella Regulates the Development of Female Germline Stem Cells by Modulating Chromatin Structure and DNA Methylation |
title_sort | stella regulates the development of female germline stem cells by modulating chromatin structure and dna methylation |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9066111/ https://www.ncbi.nlm.nih.gov/pubmed/35541912 http://dx.doi.org/10.7150/ijbs.69240 |
work_keys_str_mv | AT houchangliang stellaregulatesthedevelopmentoffemalegermlinestemcellsbymodulatingchromatinstructureanddnamethylation AT zhaoxinyan stellaregulatesthedevelopmentoffemalegermlinestemcellsbymodulatingchromatinstructureanddnamethylation AT tiangengg stellaregulatesthedevelopmentoffemalegermlinestemcellsbymodulatingchromatinstructureanddnamethylation AT wuji stellaregulatesthedevelopmentoffemalegermlinestemcellsbymodulatingchromatinstructureanddnamethylation |