bHLH-Orange Transcription Factors in Development and Cancer.

Translational oncogenomics Pub Date : 2007-12-10 Print Date: 2007-01-01 DOI:10.4137/tog.s436
Hong Sun, Saghi Ghaffari, Reshma Taneja
{"title":"bHLH-Orange Transcription Factors in Development and Cancer.","authors":"Hong Sun,&nbsp;Saghi Ghaffari,&nbsp;Reshma Taneja","doi":"10.4137/tog.s436","DOIUrl":null,"url":null,"abstract":"<p><p>Basic helix-loop-helix (bHLH) proteins are a large superfamily of transcription factors that play critical roles in many physiological processes including cellular differentiation, cell cycle arrest and apoptosis. Based on structural and phylogenetic analysis, mammalian bHLH-Orange (bHLH-O) proteins, which constitute the repressor family of bHLH factors, can be grouped into four subfamilies: Hes, Hey, Helt and Stra13/Dec. In addition to the bHLH domain that mediates DNA-binding and protein dimerization, all members of this family are characterized by a distinctive motif called the \"Orange domain\" which is present exclusively in these factors. Genetic studies using targeted mutagenesis in mice have revealed essential roles for many bHLH-O genes in embryonic development, cell fate decisions, differentiation of a number of cell types and in apoptosis. Furthermore, growing evidence of crosstalk between bHLH-O proteins with the tumor suppressors p53 and hypoxia-inducible factor, have started to shed light on their possible roles in oncogenesis. Consistently, deregulated expression of several bHLH-O factors is associated with various human cancers. Here, we review the structure and biological functions of bHLH-O factors, and discuss recent studies that suggest a potential role for these factors in tumorigenesis and tumor progression.</p>","PeriodicalId":88783,"journal":{"name":"Translational oncogenomics","volume":"2 ","pages":"107-20"},"PeriodicalIF":0.0000,"publicationDate":"2007-12-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3634620/pdf/","citationCount":"48","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Translational oncogenomics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4137/tog.s436","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2007/1/1 0:00:00","PubModel":"Print","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 48

Abstract

Basic helix-loop-helix (bHLH) proteins are a large superfamily of transcription factors that play critical roles in many physiological processes including cellular differentiation, cell cycle arrest and apoptosis. Based on structural and phylogenetic analysis, mammalian bHLH-Orange (bHLH-O) proteins, which constitute the repressor family of bHLH factors, can be grouped into four subfamilies: Hes, Hey, Helt and Stra13/Dec. In addition to the bHLH domain that mediates DNA-binding and protein dimerization, all members of this family are characterized by a distinctive motif called the "Orange domain" which is present exclusively in these factors. Genetic studies using targeted mutagenesis in mice have revealed essential roles for many bHLH-O genes in embryonic development, cell fate decisions, differentiation of a number of cell types and in apoptosis. Furthermore, growing evidence of crosstalk between bHLH-O proteins with the tumor suppressors p53 and hypoxia-inducible factor, have started to shed light on their possible roles in oncogenesis. Consistently, deregulated expression of several bHLH-O factors is associated with various human cancers. Here, we review the structure and biological functions of bHLH-O factors, and discuss recent studies that suggest a potential role for these factors in tumorigenesis and tumor progression.

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
bhlh -橙色转录因子在发育和癌症中的作用。
碱性螺旋-环-螺旋(bHLH)蛋白是一个庞大的转录因子超家族,在细胞分化、细胞周期阻滞和细胞凋亡等许多生理过程中发挥关键作用。根据结构和系统发育分析,哺乳动物bHLH- orange (bHLH- o)蛋白构成bHLH因子抑制家族,可分为Hes、Hey、Helt和Stra13/Dec四个亚家族。除了介导dna结合和蛋白质二聚化的bHLH结构域外,该家族的所有成员都具有独特的基元,称为“橙色结构域”,仅存在于这些因子中。在小鼠中使用靶向诱变的遗传学研究揭示了许多bHLH-O基因在胚胎发育、细胞命运决定、多种细胞类型的分化和凋亡中的重要作用。此外,越来越多的证据表明bHLH-O蛋白与肿瘤抑制因子p53和缺氧诱导因子之间的串扰,已经开始阐明它们在肿瘤发生中的可能作用。一致地,几种bHLH-O因子的表达失调与各种人类癌症有关。在这里,我们回顾了bHLH-O因子的结构和生物学功能,并讨论了最近的研究表明这些因子在肿瘤发生和肿瘤进展中的潜在作用。
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
自引率
0.00%
发文量
0
期刊最新文献
Advances in Sarcoma Genomics and Therapeutic Management Single Nucleotide Polymorphisms in Cancer Research and Treatment Rationale for Immunotherapy in Gastrointestinal Malignancies Proteomics Profiling of Pancreatic Cancer Molecular Pathways in Melanomagenesis
×
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