The CoREST complex regulates multiple histone modifications temporal-specifically in clock neurons.

IF 4.5 3区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Open Biology Pub Date : 2024-07-01 Epub Date: 2024-07-10 DOI:10.1098/rsob.230355
Pengfei Lv, Zhangwu Zhao, Yukinori Hirano, Juan Du
{"title":"The CoREST complex regulates multiple histone modifications temporal-specifically in clock neurons.","authors":"Pengfei Lv, Zhangwu Zhao, Yukinori Hirano, Juan Du","doi":"10.1098/rsob.230355","DOIUrl":null,"url":null,"abstract":"<p><p>Epigenetic regulation is important for circadian rhythm. In previous studies, multiple histone modifications were found at the <i>Period</i> (<i>Per</i>) locus. However, most of these studies were not conducted in clock neurons. In our screen, we found that a <i>CoREST</i> mutation resulted in defects in circadian rhythm by affecting <i>Per</i> transcription. Based on previous studies, we hypothesized that <i>CoREST</i> regulates circadian rhythm by regulating multiple histone modifiers at the <i>Per</i> locus. Genetic and physical interaction experiments supported these regulatory relationships. Moreover, through tissue-specific chromatin immunoprecipitation assays in clock neurons, we found that the <i>CoREST</i> mutation led to time-dependent changes in corresponding histone modifications at the <i>Per</i> locus. Finally, we proposed a model indicating the role of the CoREST complex in the regulation of circadian rhythm. This study revealed the dynamic changes of histone modifications at the <i>Per</i> locus specifically in clock neurons. Importantly, it provides insights into the role of epigenetic factors in the regulation of dynamic gene expression changes in circadian rhythm.</p>","PeriodicalId":19629,"journal":{"name":"Open Biology","volume":"14 7","pages":"230355"},"PeriodicalIF":4.5000,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11285899/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Open Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1098/rsob.230355","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/7/10 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Epigenetic regulation is important for circadian rhythm. In previous studies, multiple histone modifications were found at the Period (Per) locus. However, most of these studies were not conducted in clock neurons. In our screen, we found that a CoREST mutation resulted in defects in circadian rhythm by affecting Per transcription. Based on previous studies, we hypothesized that CoREST regulates circadian rhythm by regulating multiple histone modifiers at the Per locus. Genetic and physical interaction experiments supported these regulatory relationships. Moreover, through tissue-specific chromatin immunoprecipitation assays in clock neurons, we found that the CoREST mutation led to time-dependent changes in corresponding histone modifications at the Per locus. Finally, we proposed a model indicating the role of the CoREST complex in the regulation of circadian rhythm. This study revealed the dynamic changes of histone modifications at the Per locus specifically in clock neurons. Importantly, it provides insights into the role of epigenetic factors in the regulation of dynamic gene expression changes in circadian rhythm.

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
CoREST复合体在时钟神经元中调节多种组蛋白修饰的时间特异性。
表观遗传调控对昼夜节律非常重要。以往的研究发现,Per(周期)基因座存在多种组蛋白修饰。然而,这些研究大多不是在时钟神经元中进行的。在我们的筛选中,我们发现 CoREST 突变会影响 Per 的转录,从而导致昼夜节律缺陷。基于之前的研究,我们假设 CoREST 通过调节 Per 基因座上的多个组蛋白修饰因子来调节昼夜节律。遗传和物理相互作用实验证实了这些调控关系。此外,通过在时钟神经元中进行组织特异性染色质免疫沉淀实验,我们发现 CoREST 突变会导致 Per 基因座上相应组蛋白修饰的时间依赖性变化。最后,我们提出了一个模型,表明了CoREST复合物在昼夜节律调控中的作用。这项研究揭示了Per基因座组蛋白修饰在时钟神经元中的动态变化。重要的是,它提供了关于表观遗传因素在调控昼夜节律动态基因表达变化中的作用的见解。
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
Open Biology
Open Biology BIOCHEMISTRY & MOLECULAR BIOLOGY-
CiteScore
10.00
自引率
1.70%
发文量
136
审稿时长
6-12 weeks
期刊介绍: Open Biology is an online journal that welcomes original, high impact research in cell and developmental biology, molecular and structural biology, biochemistry, neuroscience, immunology, microbiology and genetics.
期刊最新文献
Axon demyelination and degeneration in a zebrafish spastizin model of hereditary spastic paraplegia. Cebpa is required for haematopoietic stem and progenitor cell generation and maintenance in zebrafish. SID-2 is a conserved extracellular vesicle protein that is not associated with environmental RNAi in parasitic nematodes. Mathematical model of RNA-directed DNA methylation predicts tuning of negative feedback required for stable maintenance. Learning-induced remodelling of inhibitory synapses in the motor cortex.
×
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