先锋转录因子Zelda控制着果蝇再生和模式恢复的退出

IF 12.5 1区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES
Anish Bose, Keaton Schuster, Chandril Kodali, Surabhi Sonam, Rachel K. Smith-Bolton
{"title":"先锋转录因子Zelda控制着果蝇再生和模式恢复的退出","authors":"Anish Bose,&nbsp;Keaton Schuster,&nbsp;Chandril Kodali,&nbsp;Surabhi Sonam,&nbsp;Rachel K. Smith-Bolton","doi":"10.1126/sciadv.ads5743","DOIUrl":null,"url":null,"abstract":"<div >Many animals can regenerate tissues after injury. While the initiation of regeneration has been studied extensively, how the damage response ends and normal gene expression returns is unclear. We found that in <i>Drosophila</i> wing imaginal discs, the pioneer transcription factor Zelda controls the exit from regeneration and return to normal gene expression. Optogenetic inactivation of Zelda during regeneration disrupted patterning, induced cell fate errors, and caused morphological defects yet had no effect on normal wing development. Using Cleavage Under Targets &amp; Release Using Nuclease, we identified targets of Zelda important for the end of regeneration, including genes that control wing margin and vein specification, compartment identity, and cell adhesion. We also found that GAGA factor and Fork head similarly coordinate patterning after regeneration and that chromatin regions bound by Zelda increase in accessibility during regeneration. Thus, Zelda orchestrates the transition from regeneration to normal gene expression, highlighting a fundamental difference between developmental and regeneration patterning in the wing disc.</div>","PeriodicalId":21609,"journal":{"name":"Science Advances","volume":"11 23","pages":""},"PeriodicalIF":12.5000,"publicationDate":"2025-06-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.science.org/doi/reader/10.1126/sciadv.ads5743","citationCount":"0","resultStr":"{\"title\":\"The pioneer transcription factor Zelda controls the exit from regeneration and restoration of patterning in Drosophila\",\"authors\":\"Anish Bose,&nbsp;Keaton Schuster,&nbsp;Chandril Kodali,&nbsp;Surabhi Sonam,&nbsp;Rachel K. Smith-Bolton\",\"doi\":\"10.1126/sciadv.ads5743\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div >Many animals can regenerate tissues after injury. While the initiation of regeneration has been studied extensively, how the damage response ends and normal gene expression returns is unclear. We found that in <i>Drosophila</i> wing imaginal discs, the pioneer transcription factor Zelda controls the exit from regeneration and return to normal gene expression. Optogenetic inactivation of Zelda during regeneration disrupted patterning, induced cell fate errors, and caused morphological defects yet had no effect on normal wing development. Using Cleavage Under Targets &amp; Release Using Nuclease, we identified targets of Zelda important for the end of regeneration, including genes that control wing margin and vein specification, compartment identity, and cell adhesion. We also found that GAGA factor and Fork head similarly coordinate patterning after regeneration and that chromatin regions bound by Zelda increase in accessibility during regeneration. Thus, Zelda orchestrates the transition from regeneration to normal gene expression, highlighting a fundamental difference between developmental and regeneration patterning in the wing disc.</div>\",\"PeriodicalId\":21609,\"journal\":{\"name\":\"Science Advances\",\"volume\":\"11 23\",\"pages\":\"\"},\"PeriodicalIF\":12.5000,\"publicationDate\":\"2025-06-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.science.org/doi/reader/10.1126/sciadv.ads5743\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Science Advances\",\"FirstCategoryId\":\"103\",\"ListUrlMain\":\"https://www.science.org/doi/10.1126/sciadv.ads5743\",\"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}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Science Advances","FirstCategoryId":"103","ListUrlMain":"https://www.science.org/doi/10.1126/sciadv.ads5743","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

摘要

许多动物受伤后能使组织再生。虽然再生的启动已经被广泛研究,但损伤反应如何结束和正常基因表达如何恢复尚不清楚。我们发现,在果蝇的翅膀想象盘中,先锋转录因子Zelda控制着再生退出和正常基因表达的回归。在再生过程中,Zelda的光遗传失活破坏了模式,诱导了细胞命运错误,造成了形态缺陷,但对正常的翅膀发育没有影响。在目标下使用乳沟利用核酸酶,我们确定了Zelda对再生结束的重要目标,包括控制翼缘和静脉规格、室识别和细胞粘附的基因。我们还发现再生后GAGA因子和叉头相似的协调模式,并且Zelda结合的染色质区域在再生过程中可接近性增加。因此,塞尔达协调了从再生到正常基因表达的转变,强调了翼盘发育和再生模式之间的根本区别。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The pioneer transcription factor Zelda controls the exit from regeneration and restoration of patterning in Drosophila

The pioneer transcription factor Zelda controls the exit from regeneration and restoration of patterning in Drosophila
Many animals can regenerate tissues after injury. While the initiation of regeneration has been studied extensively, how the damage response ends and normal gene expression returns is unclear. We found that in Drosophila wing imaginal discs, the pioneer transcription factor Zelda controls the exit from regeneration and return to normal gene expression. Optogenetic inactivation of Zelda during regeneration disrupted patterning, induced cell fate errors, and caused morphological defects yet had no effect on normal wing development. Using Cleavage Under Targets & Release Using Nuclease, we identified targets of Zelda important for the end of regeneration, including genes that control wing margin and vein specification, compartment identity, and cell adhesion. We also found that GAGA factor and Fork head similarly coordinate patterning after regeneration and that chromatin regions bound by Zelda increase in accessibility during regeneration. Thus, Zelda orchestrates the transition from regeneration to normal gene expression, highlighting a fundamental difference between developmental and regeneration patterning in the wing disc.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
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