The gene regulatory landscape driving mouse gonadal supporting cell differentiation

IF 11.7 1区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES
Isabelle Stévant, Elisheva Abberbock, Meshi Ridnik, Roni Weiss, Linoy Swisa, Christopher R. Futtner, Danielle M. Maatouk, Robin Lovell-Badge, Valeriya Malysheva, Nitzan Gonen
{"title":"The gene regulatory landscape driving mouse gonadal supporting cell differentiation","authors":"Isabelle Stévant,&nbsp;Elisheva Abberbock,&nbsp;Meshi Ridnik,&nbsp;Roni Weiss,&nbsp;Linoy Swisa,&nbsp;Christopher R. Futtner,&nbsp;Danielle M. Maatouk,&nbsp;Robin Lovell-Badge,&nbsp;Valeriya Malysheva,&nbsp;Nitzan Gonen","doi":"10.1126/sciadv.adv1885","DOIUrl":null,"url":null,"abstract":"<div >Gonadal sex determination relies on tipping a delicate balance involving the activation and repression of several transcription factors and signaling pathways. This is likely mediated by numerous noncoding regulatory elements that shape sex-specific transcriptomic programs. To explore the dynamics of these in detail, we performed paired time series of transcriptomic and chromatin accessibility assays on pre-granulosa and Sertoli cells throughout their development in the embryo, making use of new and existing mouse reporter lines. Regulatory elements were associated with their putative target genes by linkage analysis, and this was complemented and verified experimentally using promoter capture Hi-C. We identified the transcription factor motifs enriched in these regulatory elements along with their occupancy, pinpointing LHX9/EMX2 as potentially critical regulators of ovarian development. Variations in the DNA sequence of these regulatory elements are likely to be responsible for many of the unexplained cases of individuals with differences of sex development.</div>","PeriodicalId":21609,"journal":{"name":"Science Advances","volume":"11 30","pages":""},"PeriodicalIF":11.7000,"publicationDate":"2025-07-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.science.org/doi/reader/10.1126/sciadv.adv1885","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Science Advances","FirstCategoryId":"103","ListUrlMain":"https://www.science.org/doi/10.1126/sciadv.adv1885","RegionNum":1,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Gonadal sex determination relies on tipping a delicate balance involving the activation and repression of several transcription factors and signaling pathways. This is likely mediated by numerous noncoding regulatory elements that shape sex-specific transcriptomic programs. To explore the dynamics of these in detail, we performed paired time series of transcriptomic and chromatin accessibility assays on pre-granulosa and Sertoli cells throughout their development in the embryo, making use of new and existing mouse reporter lines. Regulatory elements were associated with their putative target genes by linkage analysis, and this was complemented and verified experimentally using promoter capture Hi-C. We identified the transcription factor motifs enriched in these regulatory elements along with their occupancy, pinpointing LHX9/EMX2 as potentially critical regulators of ovarian development. Variations in the DNA sequence of these regulatory elements are likely to be responsible for many of the unexplained cases of individuals with differences of sex development.

Abstract Image

驱动小鼠性腺支持细胞分化的基因调控景观
性腺性别的决定依赖于一种微妙的平衡,这种平衡涉及几个转录因子和信号通路的激活和抑制。这可能是由许多形成性别特异性转录组程序的非编码调控元件介导的。为了详细探索这些动态,我们利用新的和现有的小鼠报告系,对颗粒前细胞和支持细胞在胚胎发育过程中进行了成对的转录组学和染色质可及性分析。通过连锁分析,调控元件与其假定的靶基因相关联,并通过启动子捕获Hi-C进行了补充和实验验证。我们确定了这些调控元件及其占用中富集的转录因子基序,确定了LHX9/EMX2是卵巢发育的潜在关键调控因子。这些调节元件的DNA序列的变化很可能是许多无法解释的个体性发育差异的原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Science Advances
Science Advances 综合性期刊-综合性期刊
CiteScore
21.40
自引率
1.50%
发文量
1937
审稿时长
29 weeks
期刊介绍: Science Advances, an open-access journal by AAAS, publishes impactful research in diverse scientific areas. It aims for fair, fast, and expert peer review, providing freely accessible research to readers. Led by distinguished scientists, the journal supports AAAS's mission by extending Science magazine's capacity to identify and promote significant advances. Evolving digital publishing technologies play a crucial role in advancing AAAS's global mission for science communication and benefitting humankind.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信