ZNF750 is a p63 target gene that induces KLF4 to drive terminal epidermal differentiation.

IF 10.7 1区 生物学 Q1 CELL BIOLOGY Developmental cell Pub Date : 2012-03-13 Epub Date: 2012-02-23 DOI:10.1016/j.devcel.2011.12.001
George L Sen, Lisa D Boxer, Dan E Webster, Rose T Bussat, Kun Qu, Brian J Zarnegar, Danielle Johnston, Zurab Siprashvili, Paul A Khavari
{"title":"ZNF750 is a p63 target gene that induces KLF4 to drive terminal epidermal differentiation.","authors":"George L Sen,&nbsp;Lisa D Boxer,&nbsp;Dan E Webster,&nbsp;Rose T Bussat,&nbsp;Kun Qu,&nbsp;Brian J Zarnegar,&nbsp;Danielle Johnston,&nbsp;Zurab Siprashvili,&nbsp;Paul A Khavari","doi":"10.1016/j.devcel.2011.12.001","DOIUrl":null,"url":null,"abstract":"<p><p>Disrupted epidermal differentiation characterizes numerous diseases that impact >25% of the population. In a search for dominant mediators of differentiation, we defined a requirement for ZNF750 in terminal epidermal differentiation. ZNF750 controlled genes mutated in numerous human skin diseases, including FLG, LOR, LCE3B, ALOXE3, and SPINK5. ZNF750 induced progenitor differentiation via an evolutionarily conserved C2H2 zinc finger motif. The epidermal master regulator, p63, bound the ZNF750 promoter and was necessary for its induction. ZNF750 restored differentiation to p63-deficient tissue, suggesting that it acts downstream of p63. A search for functionally important ZNF750 targets via analysis of ZNF750-regulated genes identified KLF4, a transcription factor that activates late epidermal differentiation. ZNF750 binds to KLF4 at multiple sites flanking the transcriptional start site and controls its expression. ZNF750 thus directly links a tissue-specifying factor, p63, to an effector of terminal differentiation, KLF4, and represents a potential future target for disorders of this process.</p>","PeriodicalId":11157,"journal":{"name":"Developmental cell","volume":null,"pages":null},"PeriodicalIF":10.7000,"publicationDate":"2012-03-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.devcel.2011.12.001","citationCount":"193","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Developmental cell","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1016/j.devcel.2011.12.001","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2012/2/23 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 193

Abstract

Disrupted epidermal differentiation characterizes numerous diseases that impact >25% of the population. In a search for dominant mediators of differentiation, we defined a requirement for ZNF750 in terminal epidermal differentiation. ZNF750 controlled genes mutated in numerous human skin diseases, including FLG, LOR, LCE3B, ALOXE3, and SPINK5. ZNF750 induced progenitor differentiation via an evolutionarily conserved C2H2 zinc finger motif. The epidermal master regulator, p63, bound the ZNF750 promoter and was necessary for its induction. ZNF750 restored differentiation to p63-deficient tissue, suggesting that it acts downstream of p63. A search for functionally important ZNF750 targets via analysis of ZNF750-regulated genes identified KLF4, a transcription factor that activates late epidermal differentiation. ZNF750 binds to KLF4 at multiple sites flanking the transcriptional start site and controls its expression. ZNF750 thus directly links a tissue-specifying factor, p63, to an effector of terminal differentiation, KLF4, and represents a potential future target for disorders of this process.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
ZNF750是p63靶基因,可诱导KLF4驱动终表皮分化。
表皮分化中断是影响25%以上人群的许多疾病的特征。为了寻找主要的分化介质,我们确定了ZNF750在终表皮分化中的要求。ZNF750控制了许多人类皮肤病的突变基因,包括FLG、LOR、LCE3B、ALOXE3和SPINK5。ZNF750通过一个进化保守的C2H2锌指基序诱导祖细胞分化。表皮主调控因子p63结合ZNF750启动子,是诱导ZNF750启动子的必要条件。ZNF750恢复了p63缺失组织的分化,表明它作用于p63的下游。通过分析ZNF750调控基因寻找功能重要的ZNF750靶点,发现了KLF4,这是一种激活表皮晚期分化的转录因子。ZNF750在转录起始位点的多个位点与KLF4结合并控制其表达。因此,ZNF750直接将组织指定因子p63与终末分化效应因子KLF4联系起来,并代表了该过程紊乱的潜在未来靶点。
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 去求助
来源期刊
Developmental cell
Developmental cell 生物-发育生物学
CiteScore
18.90
自引率
1.70%
发文量
203
审稿时长
3-6 weeks
期刊介绍: Developmental Cell, established in 2001, is a comprehensive journal that explores a wide range of topics in cell and developmental biology. Our publication encompasses work across various disciplines within biology, with a particular emphasis on investigating the intersections between cell biology, developmental biology, and other related fields. Our primary objective is to present research conducted through a cell biological perspective, addressing the essential mechanisms governing cell function, cellular interactions, and responses to the environment. Moreover, we focus on understanding the collective behavior of cells, culminating in the formation of tissues, organs, and whole organisms, while also investigating the consequences of any malfunctions in these intricate processes.
期刊最新文献
Axon guidance during mouse central nervous system regeneration is required for specific brain innervation An ILK/STAT3 pathway controls glioblastoma stem cell plasticity Partial closure of the γ-tubulin ring complex by CDK5RAP2 activates microtubule nucleation CDK5RAP2 activates microtubule nucleator γTuRC by facilitating template formation and actin release Creating a path during melanoma amoeboid migration: When too crowded, start worrying
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1