• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
RAD53, DUN1 and PDS1 define two parallel G2/M checkpoint pathways in budding yeast.RAD53、DUN1和PDS1在芽殖酵母中定义了两条平行的G2/M期检验点通路。
EMBO J. 1999 Jun 1;18(11):3173-85. doi: 10.1093/emboj/18.11.3173.
2
Activation of the budding yeast securin Pds1 but not Rad53 correlates with double-strand break-associated G2/M cell cycle arrest in a mec1 hypomorphic mutant.在mec1低表达突变体中,出芽酵母securin Pds1的激活而非Rad53的激活与双链断裂相关的G2/M期细胞周期阻滞有关。
Cell Cycle. 2007 Aug 1;6(15):1896-902. doi: 10.4161/cc.6.15.4510. Epub 2007 May 25.
3
RAD9 and RAD24 define two additive, interacting branches of the DNA damage checkpoint pathway in budding yeast normally required for Rad53 modification and activation.RAD9和RAD24定义了芽殖酵母中DNA损伤检查点途径的两个相加且相互作用的分支,这两个分支通常是Rad53修饰和激活所必需的。
EMBO J. 1998 May 1;17(9):2687-98. doi: 10.1093/emboj/17.9.2687.
4
Two distinct pathways for inhibiting pds1 ubiquitination in response to DNA damage.响应DNA损伤时抑制Pds1泛素化的两条不同途径。
J Biol Chem. 2003 Nov 7;278(45):45027-33. doi: 10.1074/jbc.M306783200. Epub 2003 Aug 28.
5
Control of the DNA damage checkpoint by chk1 and rad53 protein kinases through distinct mechanisms.chk1和rad53蛋白激酶通过不同机制对DNA损伤检查点进行调控。
Science. 1999 Nov 5;286(5442):1166-71. doi: 10.1126/science.286.5442.1166.
6
A Tel1/MRX-dependent checkpoint inhibits the metaphase-to-anaphase transition after UV irradiation in the absence of Mec1.在缺乏Mec1的情况下,一种依赖Tel1/MRX的检查点会在紫外线照射后抑制中期到后期的转变。
Mol Cell Biol. 2004 Dec;24(23):10126-44. doi: 10.1128/MCB.24.23.10126-10144.2004.
7
Saccharomyces cerevisiae RAD53 (CHK2) but not CHK1 is required for double-strand break-initiated SCE and DNA damage-associated SCE after exposure to X rays and chemical agents.酿酒酵母RAD53(CHK2)而非CHK1是暴露于X射线和化学试剂后双链断裂引发的姐妹染色单体交换(SCE)以及与DNA损伤相关的SCE所必需的。
DNA Repair (Amst). 2005 Nov 21;4(11):1240-51. doi: 10.1016/j.dnarep.2005.06.006. Epub 2005 Jul 21.
8
Dun1, a Chk2-related kinase, is the central regulator of securin-separase dynamics during DNA damage signaling.邓 1 号,一种 Chk2 相关激酶,是 DNA 损伤信号传导过程中 securin-separase 动态的中央调节因子。
Nucleic Acids Res. 2020 Jun 19;48(11):6092-6107. doi: 10.1093/nar/gkaa355.
9
The Saccharomyces cerevisiae checkpoint genes RAD9, CHK1 and PDS1 are required for elevated homologous recombination in a mec1 (ATR) hypomorphic mutant.酿酒酵母检查点基因RAD9、CHK1和PDS1是mec1(ATR)亚效突变体中同源重组增加所必需的。
Cell Cycle. 2008 Aug;7(15):2418-26. doi: 10.4161/cc.6411. Epub 2008 Jun 9.
10
Distinct roles of yeast MEC and RAD checkpoint genes in transcriptional induction after DNA damage and implications for function.酵母MEC和RAD检查点基因在DNA损伤后转录诱导中的不同作用及其功能意义
Mol Biol Cell. 1996 May;7(5):703-18. doi: 10.1091/mbc.7.5.703.

引用本文的文献

1
DNA Damage Checkpoints Govern Global Gene Transcription and Exhibit Species-Specific Regulation on in .DNA损伤检查点调控全局基因转录并在……中表现出物种特异性调控 。 (你提供的原文似乎不完整,“on in.”表述有误,可能影响准确理解。)
J Fungi (Basel). 2024 May 29;10(6):387. doi: 10.3390/jof10060387.
2
The increase in cell death rates in caloric restricted cells of the yeast helicase mutant rrm3 is Sir complex dependent.热量限制条件下酵母解旋酶突变体 rrm3 细胞死亡率的增加依赖于 Sir 复合物。
Sci Rep. 2023 Oct 19;13(1):17832. doi: 10.1038/s41598-023-45125-z.
3
Coupling DNA Replication and Spindle Function in .在. 中连接 DNA 复制和纺锤体功能
Cells. 2021 Nov 30;10(12):3359. doi: 10.3390/cells10123359.
4
Dun1, a Chk2-related kinase, is the central regulator of securin-separase dynamics during DNA damage signaling.邓 1 号,一种 Chk2 相关激酶,是 DNA 损伤信号传导过程中 securin-separase 动态的中央调节因子。
Nucleic Acids Res. 2020 Jun 19;48(11):6092-6107. doi: 10.1093/nar/gkaa355.
5
Checkpoint Responses to DNA Double-Strand Breaks.DNA 双链断裂的检查点反应。
Annu Rev Biochem. 2020 Jun 20;89:103-133. doi: 10.1146/annurev-biochem-011520-104722. Epub 2020 Mar 16.
6
Regulation of Mitotic Exit by Cell Cycle Checkpoints: Lessons From .细胞周期检查点对有丝分裂后期的调控:来自. 的启示。
Genes (Basel). 2020 Feb 12;11(2):195. doi: 10.3390/genes11020195.
7
Inhibition of spindle extension through the yeast S phase checkpoint is coupled to replication fork stability and the integrity of centromeric DNA.通过酵母 S 期检查点抑制纺锤体延伸与复制叉稳定性和着丝粒 DNA 的完整性相关联。
Mol Biol Cell. 2019 Oct 15;30(22):2771-2789. doi: 10.1091/mbc.E19-03-0156. Epub 2019 Sep 11.
8
S-phase checkpoint regulations that preserve replication and chromosome integrity upon dNTP depletion.在脱氧核苷酸三磷酸(dNTP)耗竭时维持复制和染色体完整性的S期检查点调控。
Cell Mol Life Sci. 2017 Jul;74(13):2361-2380. doi: 10.1007/s00018-017-2474-4. Epub 2017 Feb 20.
9
Asf1 facilitates dephosphorylation of Rad53 after DNA double-strand break repair.在DNA双链断裂修复后,Asf1促进Rad53的去磷酸化。
Genes Dev. 2016 May 15;30(10):1211-24. doi: 10.1101/gad.280685.116.
10
The eukaryotic protein kinase superfamily of the necrotrophic fungal plant pathogen, Sclerotinia sclerotiorum.坏死营养型真菌植物病原菌核盘菌的真核蛋白激酶超家族。
Mol Plant Pathol. 2016 May;17(4):634-47. doi: 10.1111/mpp.12321. Epub 2015 Dec 8.

本文引用的文献

1
Analysis of Rad3 and Chk1 protein kinases defines different checkpoint responses.对Rad3和Chk1蛋白激酶的分析确定了不同的检查点反应。
EMBO J. 1998 Dec 15;17(24):7239-49. doi: 10.1093/emboj/17.24.7239.
2
A suppressor of two essential checkpoint genes identifies a novel protein that negatively affects dNTP pools.两个关键检查点基因的一个抑制因子鉴定出一种对脱氧核苷酸三磷酸库产生负面影响的新蛋白质。
Mol Cell. 1998 Sep;2(3):329-40. doi: 10.1016/s1097-2765(00)80277-4.
3
The budding yeast Rad9 checkpoint protein is subjected to Mec1/Tel1-dependent hyperphosphorylation and interacts with Rad53 after DNA damage.出芽酵母Rad9检查点蛋白会经历Mec1/Tel1依赖性的过度磷酸化,并在DNA损伤后与Rad53相互作用。
EMBO J. 1998 Oct 1;17(19):5679-88. doi: 10.1093/emboj/17.19.5679.
4
DNA damage checkpoint in budding yeast.芽殖酵母中的DNA损伤检查点。
EMBO J. 1998 Oct 1;17(19):5525-8. doi: 10.1093/emboj/17.19.5525.
5
Recovery from DNA replicational stress is the essential function of the S-phase checkpoint pathway.从DNA复制应激中恢复是S期检查点通路的基本功能。
Genes Dev. 1998 Sep 15;12(18):2956-70. doi: 10.1101/gad.12.18.2956.
6
The DNA replication and damage checkpoint pathways induce transcription by inhibition of the Crt1 repressor.DNA复制和损伤检查点途径通过抑制Crt1阻遏物来诱导转录。
Cell. 1998 Sep 4;94(5):595-605. doi: 10.1016/s0092-8674(00)81601-3.
7
MEC1-dependent phosphorylation of Rad9p in response to DNA damage.响应DNA损伤时,Rad9p的MEC1依赖性磷酸化。
Mol Cell. 1998 Aug;2(2):183-9. doi: 10.1016/s1097-2765(00)80128-8.
8
Mec1p is essential for phosphorylation of the yeast DNA damage checkpoint protein Ddc1p, which physically interacts with Mec3p.Mec1p对于酵母DNA损伤检查点蛋白Ddc1p的磷酸化至关重要,而Ddc1p与Mec3p存在物理相互作用。
EMBO J. 1998 Jul 15;17(14):4199-209. doi: 10.1093/emboj/17.14.4199.
9
Rad53 FHA domain associated with phosphorylated Rad9 in the DNA damage checkpoint.在DNA损伤检查点中,Rad53 FHA结构域与磷酸化的Rad9相关联。
Science. 1998 Jul 10;281(5374):272-4. doi: 10.1126/science.281.5374.272.
10
An ESP1/PDS1 complex regulates loss of sister chromatid cohesion at the metaphase to anaphase transition in yeast.一种ESP1/PDS1复合物在酵母中期到后期转换过程中调节姐妹染色单体黏连的丧失。
Cell. 1998 Jun 12;93(6):1067-76. doi: 10.1016/s0092-8674(00)81211-8.

RAD53、DUN1和PDS1在芽殖酵母中定义了两条平行的G2/M期检验点通路。

RAD53, DUN1 and PDS1 define two parallel G2/M checkpoint pathways in budding yeast.

作者信息

Gardner R, Putnam C W, Weinert T

机构信息

Department of Molecular and Cellular Biology, The University of Arizona, PO Box 21016, Tucson, AZ 85721-0106, USA.

出版信息

EMBO J. 1999 Jun 1;18(11):3173-85. doi: 10.1093/emboj/18.11.3173.

DOI:10.1093/emboj/18.11.3173
PMID:10357828
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1171398/
Abstract

Eukaryotic checkpoint genes regulate multiple cellular responses to DNA damage. In this report, we examine the roles of budding yeast genes involved in G2/M arrest and tolerance to UV exposure. A current model posits three gene classes: those encoding proteins acting on damaged DNA (e.g. RAD9 and RAD24), those transducing a signal (MEC1, RAD53 and DUN1) or those participating more directly in arrest (PDS1). Here, we define important features of the pathways subserved by those genes. MEC1, which we find is required for both establishment and maintenance of G2/M arrest, mediates this arrest through two parallel pathways. One pathway requires RAD53 and DUN1 (the 'RAD53 pathway'); the other pathway requires PDS1. Each pathway independently contributes approximately 50% to G2/M arrest, effects demonstrable after cdc13-induced damage or a double-stranded break inflicted by the HO endonuclease. Similarly, both pathways contribute independently to tolerance of UV irradiation. How the parallel pathways might interact ultimately to achieve arrest is not yet understood, but we do provide evidence that neither the RAD53 nor the PDS1 pathway appears to maintain arrest by inhibiting adaptation. Instead, we think it likely that both pathways contribute to establishing and maintaining arrest.

摘要

真核生物的检查点基因调控细胞对DNA损伤的多种反应。在本报告中,我们研究了芽殖酵母中参与G2/M期阻滞和对紫外线照射耐受性的基因的作用。目前的模型提出了三类基因:一类编码作用于受损DNA的蛋白质(如RAD9和RAD24),一类转导信号(MEC1、RAD53和DUN1),还有一类更直接地参与阻滞(PDS1)。在这里,我们定义了这些基因所支持的通路的重要特征。我们发现MEC1是G2/M期阻滞的建立和维持所必需的,它通过两条平行的通路介导这种阻滞。一条通路需要RAD53和DUN1(“RAD53通路”);另一条通路需要PDS1。每条通路对G2/M期阻滞的独立贡献约为50%,这在cdc13诱导的损伤或HO内切核酸酶造成的双链断裂后得到了证实。同样,这两条通路对紫外线照射的耐受性也有独立贡献。目前尚不清楚这两条平行通路最终如何相互作用以实现阻滞,但我们确实提供了证据表明,RAD53通路和PDS1通路似乎都不是通过抑制适应来维持阻滞的。相反,我们认为这两条通路可能都有助于建立和维持阻滞。