RAD9, RAD24, RAD16 and RAD26 are required for the inducible nucleotide excision repair of UV-induced cyclobutane pyrimidine dimers from the transcribed and non-transcribed regions of the Saccharomyces cerevisiae MFA2 gene

Shirong Yu , Yumin Teng , Noel F. Lowndes , Raymond Waters
{"title":"RAD9, RAD24, RAD16 and RAD26 are required for the inducible nucleotide excision repair of UV-induced cyclobutane pyrimidine dimers from the transcribed and non-transcribed regions of the Saccharomyces cerevisiae MFA2 gene","authors":"Shirong Yu ,&nbsp;Yumin Teng ,&nbsp;Noel F. Lowndes ,&nbsp;Raymond Waters","doi":"10.1016/S0921-8777(01)00061-1","DOIUrl":null,"url":null,"abstract":"<div><p><span>In this study, the effect of a prior UV irradiation on the removal of cyclobutane pyrimidine dimers (CPDs) from the transcribed strand (TS) and non-transcribed strand (NTS) of the </span><em>MFA</em>2 gene in haploid <span><em>Saccharomyces</em><em> cerevisiae</em></span> (<em>S. cerevisiae</em>) cells was investigated. In NER competent cells, the pre-irradiation with a dose of 20<!--> <!-->J/m<sup>2</sup> enhances the removal of CPDs induced by a second UV dose of 100<!--> <!-->J/m<sup>2</sup> in the TS and the NTS of <em>MFA</em>2 gene except for the CPDs in the region +258 to +298 in the NTS, where the enhanced repair was absent. No inducible repair was observed in <em>rad9</em>, <em>rad24</em>, <em>rad16</em> and <em>rad26</em> cells, indicating two checkpoint genes <em>RAD</em>9 and <em>RAD</em>24, the global repair gene <em>RAD</em>16 and the transcription coupled repair gene <em>RAD</em>26 are essential for inducible NER.</p></div>","PeriodicalId":100935,"journal":{"name":"Mutation Research/DNA Repair","volume":"485 3","pages":"Pages 229-236"},"PeriodicalIF":0.0000,"publicationDate":"2001-04-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0921-8777(01)00061-1","citationCount":"19","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Mutation Research/DNA Repair","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0921877701000611","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 19

Abstract

In this study, the effect of a prior UV irradiation on the removal of cyclobutane pyrimidine dimers (CPDs) from the transcribed strand (TS) and non-transcribed strand (NTS) of the MFA2 gene in haploid Saccharomyces cerevisiae (S. cerevisiae) cells was investigated. In NER competent cells, the pre-irradiation with a dose of 20 J/m2 enhances the removal of CPDs induced by a second UV dose of 100 J/m2 in the TS and the NTS of MFA2 gene except for the CPDs in the region +258 to +298 in the NTS, where the enhanced repair was absent. No inducible repair was observed in rad9, rad24, rad16 and rad26 cells, indicating two checkpoint genes RAD9 and RAD24, the global repair gene RAD16 and the transcription coupled repair gene RAD26 are essential for inducible NER.

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
在Saccharomyces cerevisiae MFA2基因的转录区和非转录区,紫外线诱导的环丁烷嘧啶二聚体的核苷酸切除修复需要RAD9、RAD24、RAD16和RAD26
本研究研究了紫外线照射对单倍体酿酒酵母细胞MFA2基因转录链(TS)和非转录链(NTS)上环丁烷嘧啶二聚体(CPDs)去除的影响。在NER感态细胞中,20 J/m2的预照射增强了MFA2基因TS和NTS中第二次100 J/m2的紫外线剂量诱导的CPDs的去除,但NTS中+258至+298区域的CPDs不存在增强修复。在rad9、rad24、rad16和rad26细胞中均未观察到诱导性修复,说明两个检查点基因rad9和rad24、全局修复基因rad16和转录偶联修复基因rad26是诱导性NER的必要条件。
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
S. cerevisiae has three pathways for DNA interstrand crosslink repair Molecular characterization of ionizing radiation-hypersensitive mutant M10 cells Backbone dynamics of DNA containing 8-oxoguanine: importance for substrate recognition by base excision repair glycosylases Relationship between base excision repair capacity and DNA alkylating agent sensitivity in mouse monocytes Disruption of Xpg increases spontaneous mutation frequency, particularly A:T to C:G transversion
×
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