Survey of activation-induced genome architecture reveals a novel enhancer of Myc

IF 3.2 4区 医学 Q3 CELL BIOLOGY Immunology & Cell Biology Pub Date : 2023-01-30 DOI:10.1111/imcb.12626
Wing Fuk Chan, Hannah D Coughlan, Michelle Ruhle, Nadia Iannarella, Carolina Alvarado, Joanna R Groom, Christine R Keenan, Andrew J Kueh, Adam K Wheatley, Gordon K Smyth, Rhys S Allan, Timothy M Johanson
{"title":"Survey of activation-induced genome architecture reveals a novel enhancer of Myc","authors":"Wing Fuk Chan,&nbsp;Hannah D Coughlan,&nbsp;Michelle Ruhle,&nbsp;Nadia Iannarella,&nbsp;Carolina Alvarado,&nbsp;Joanna R Groom,&nbsp;Christine R Keenan,&nbsp;Andrew J Kueh,&nbsp;Adam K Wheatley,&nbsp;Gordon K Smyth,&nbsp;Rhys S Allan,&nbsp;Timothy M Johanson","doi":"10.1111/imcb.12626","DOIUrl":null,"url":null,"abstract":"<p>The transcription factor Myc is critically important in driving cell proliferation, a function that is frequently dysregulated in cancer. To avoid this dysregulation Myc is tightly controlled by numerous layers of regulation. One such layer is the use of distal regulatory enhancers to drive <i>Myc</i> expression. Here, using chromosome conformation capture to examine B cells of the immune system in the first hours after their activation, we reveal a previously unidentified enhancer of <i>Myc</i>. The interactivity of this enhancer coincides with a dramatic, but discrete, spike in <i>Myc</i> expression 3 h post-activation. However, genetic deletion of this region, has little impact on <i>Myc</i> expression, Myc protein level or <i>in vitro</i> and <i>in vivo</i> cell proliferation. Examination of the enhancer deleted regulatory landscape suggests that enhancer redundancy likely sustains <i>Myc</i> expression. This work highlights not only the importance of temporally examining enhancers, but also the complexity and dynamics of the regulation of critical genes such as <i>Myc</i>.</p>","PeriodicalId":179,"journal":{"name":"Immunology & Cell Biology","volume":"101 4","pages":"345-357"},"PeriodicalIF":3.2000,"publicationDate":"2023-01-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/imcb.12626","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Immunology & Cell Biology","FirstCategoryId":"2","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/imcb.12626","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

The transcription factor Myc is critically important in driving cell proliferation, a function that is frequently dysregulated in cancer. To avoid this dysregulation Myc is tightly controlled by numerous layers of regulation. One such layer is the use of distal regulatory enhancers to drive Myc expression. Here, using chromosome conformation capture to examine B cells of the immune system in the first hours after their activation, we reveal a previously unidentified enhancer of Myc. The interactivity of this enhancer coincides with a dramatic, but discrete, spike in Myc expression 3 h post-activation. However, genetic deletion of this region, has little impact on Myc expression, Myc protein level or in vitro and in vivo cell proliferation. Examination of the enhancer deleted regulatory landscape suggests that enhancer redundancy likely sustains Myc expression. This work highlights not only the importance of temporally examining enhancers, but also the complexity and dynamics of the regulation of critical genes such as Myc.

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
激活诱导的基因组结构研究揭示了一种新的Myc增强子
转录因子Myc在驱动细胞增殖中至关重要,这一功能在癌症中经常失调。为了避免这种失调,Myc受到多层调控的严格控制。其中一层是使用远端调控增强子来驱动Myc表达。在这里,利用染色体构象捕获在B细胞激活后的最初几个小时内检测免疫系统的B细胞,我们揭示了一种以前未识别的Myc增强子。这种增强子的相互作用与激活后3小时Myc表达的戏剧性但离散的峰值相吻合。然而,该区域的基因缺失,对Myc表达、Myc蛋白水平或体外和体内细胞增殖影响不大。对增强子缺失调控环境的检查表明,增强子冗余可能维持Myc表达。这项工作不仅强调了临时检查增强子的重要性,而且还强调了关键基因(如Myc)调控的复杂性和动态性。
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
Immunology & Cell Biology
Immunology & Cell Biology 医学-免疫学
CiteScore
7.50
自引率
2.50%
发文量
98
审稿时长
4-8 weeks
期刊介绍: The Australasian Society for Immunology Incorporated (ASI) was created by the amalgamation in 1991 of the Australian Society for Immunology, formed in 1970, and the New Zealand Society for Immunology, formed in 1975. The aim of the Society is to encourage and support the discipline of immunology in the Australasian region. It is a broadly based Society, embracing clinical and experimental, cellular and molecular immunology in humans and animals. The Society provides a network for the exchange of information and for collaboration within Australia, New Zealand and overseas. ASI members have been prominent in advancing biological and medical research worldwide. We seek to encourage the study of immunology in Australia and New Zealand and are active in introducing young scientists to the discipline.
期刊最新文献
Prenatal Skin Cell Atlas reveals macrophages' role beyond immunity. The journey of young scientists in Brazil: challenges and perspectives. When academia met industry: working toward a needle-free vaccination future in the sunshine state. Issue Information Choose your own T-cell fate: creation of a narrative-based, decision-making activity to engage students in immunology.
×
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