Cryo-EM structure of the CBF3-core-Ndc10-DBD complex of the budding yeast kinetochore

IF 16.8 1区 生物学 Nature Structural &Molecular Biology Pub Date : 2018-11-26 DOI:10.2210/PDB6GYP/PDB
K. Yan, Ziguo Zhang, Jing Yang, S. McLaughlin, D. Barford
{"title":"Cryo-EM structure of the CBF3-core-Ndc10-DBD complex of the budding yeast kinetochore","authors":"K. Yan, Ziguo Zhang, Jing Yang, S. McLaughlin, D. Barford","doi":"10.2210/PDB6GYP/PDB","DOIUrl":null,"url":null,"abstract":"Kinetochores are multicomponent complexes responsible for coordinating the attachment of centromeric DNA to mitotic-spindle microtubules. The point centromeres of budding yeast are organized into three centromeric determining elements (CDEs), and are associated with the centromere-specific nucleosome Cse4. Deposition of Cse4 at CEN loci is dependent on the CBF3 complex that engages CDEIII to direct Cse4 nucleosomes to CDEII. To understand how CBF3 recognizes CDEIII and positions Cse4, we determined a cryo-EM structure of a CBF3-CEN complex. CBF3 interacts with CEN DNA as a head-to-head dimer that includes the whole of CDEIII and immediate 3' regions. Specific CEN-binding of CBF3 is mediated by a Cep3 subunit of one of the CBF3 protomers that forms major groove interactions with the conserved and essential CCG and TGT motifs of CDEIII. We propose a model for a CBF3-Cse4-CEN complex with implications for understanding CBF3-directed deposition of the Cse4 nucleosome at CEN loci.","PeriodicalId":18836,"journal":{"name":"Nature Structural &Molecular Biology","volume":"25 1","pages":"1103-1110"},"PeriodicalIF":16.8000,"publicationDate":"2018-11-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nature Structural &Molecular Biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2210/PDB6GYP/PDB","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 3

Abstract

Kinetochores are multicomponent complexes responsible for coordinating the attachment of centromeric DNA to mitotic-spindle microtubules. The point centromeres of budding yeast are organized into three centromeric determining elements (CDEs), and are associated with the centromere-specific nucleosome Cse4. Deposition of Cse4 at CEN loci is dependent on the CBF3 complex that engages CDEIII to direct Cse4 nucleosomes to CDEII. To understand how CBF3 recognizes CDEIII and positions Cse4, we determined a cryo-EM structure of a CBF3-CEN complex. CBF3 interacts with CEN DNA as a head-to-head dimer that includes the whole of CDEIII and immediate 3' regions. Specific CEN-binding of CBF3 is mediated by a Cep3 subunit of one of the CBF3 protomers that forms major groove interactions with the conserved and essential CCG and TGT motifs of CDEIII. We propose a model for a CBF3-Cse4-CEN complex with implications for understanding CBF3-directed deposition of the Cse4 nucleosome at CEN loci.
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
出芽酵母着丝点CBF3-core-Ndc10-DBD复合物的低温电镜结构
着丝点是多组分复合物,负责协调着丝DNA与有丝分裂纺锤体微管的连接。出芽酵母的点着丝粒被组织成三个着丝粒决定元件(cde),并与着丝粒特异性核小体Cse4相关。Cse4在CEN位点的沉积依赖于CBF3复合物,该复合物与CDEIII结合,将Cse4核小体引导至CDEII。为了了解CBF3如何识别CDEIII并定位Cse4,我们确定了CBF3- cen配合物的低温电镜结构。CBF3与CEN DNA作为头对头二聚体相互作用,包括整个CDEIII和直接3'区。CBF3的特异性ccn结合是由CBF3原蛋白之一的Cep3亚基介导的,该亚基与CDEIII的保守和必需的CCG和TGT基序形成主要的凹槽相互作用。我们提出了一个CBF3-Cse4-CEN复合物的模型,这对理解Cse4核小体在CEN位点上的cbf3定向沉积具有重要意义。
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
Nature Structural &Molecular Biology
Nature Structural &Molecular Biology 生物-生化与分子生物学
自引率
1.80%
发文量
160
期刊介绍: Nature Structural & Molecular Biology is a monthly journal that focuses on the functional and mechanistic understanding of how molecular components in a biological process work together. It serves as an integrated forum for structural and molecular studies. The journal places a strong emphasis on the functional and mechanistic understanding of how molecular components in a biological process work together. Some specific areas of interest include the structure and function of proteins, nucleic acids, and other macromolecules, DNA replication, repair and recombination, transcription, regulation of transcription and translation, protein folding, processing and degradation, signal transduction, and intracellular signaling.
期刊最新文献
The ribosome termination complex remodels release factor RF3 and ejects GDP. Structural basis for Parkinson’s disease-linked LRRK2’s binding to microtubules Structural basis for context-specific inhibition of translation by oxazolidinone antibiotics Higher-order phosphatase–substrate contacts terminate the integrated stress response Structural basis of nucleosome transcription mediated by Chd1 and FACT
×
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