• 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
The yeast mitotic cyclin Clb2 cannot substitute for S phase cyclins in replication origin firing.酵母有丝分裂周期蛋白Clb2在复制起点激发过程中不能替代S期周期蛋白。
EMBO Rep. 2000 Dec;1(6):507-12. doi: 10.1093/embo-reports/kvd108.
2
Swe1 regulation and transcriptional control restrict the activity of mitotic cyclins toward replication proteins in Saccharomyces cerevisiae.Swe1调控和转录控制限制了酿酒酵母中有丝分裂周期蛋白对复制蛋白的活性。
Proc Natl Acad Sci U S A. 2005 Jun 21;102(25):8910-5. doi: 10.1073/pnas.0406987102. Epub 2005 Jun 14.
3
CLB5-dependent activation of late replication origins in S. cerevisiae.酿酒酵母中依赖CLB5的晚期复制起点激活。
Mol Cell. 1998 Aug;2(2):173-82. doi: 10.1016/s1097-2765(00)80127-6.
4
CLB5 and CLB6, a new pair of B cyclins involved in DNA replication in Saccharomyces cerevisiae.CLB5和CLB6,参与酿酒酵母DNA复制的一对新的B型细胞周期蛋白。
Genes Dev. 1993 Jul;7(7A):1160-75. doi: 10.1101/gad.7.7a.1160.
5
CLB5 and CLB6 are required for premeiotic DNA replication and activation of the meiotic S/M checkpoint.减数分裂前DNA复制和减数分裂S/M检查点的激活需要CLB5和CLB6。
Genes Dev. 1998 Sep 1;12(17):2698-710. doi: 10.1101/gad.12.17.2698.
6
Activation of S-phase-promoting CDKs in late G1 defines a "point of no return" after which Cdc6 synthesis cannot promote DNA replication in yeast.在G1晚期促进S期的细胞周期蛋白依赖性激酶(CDK)的激活定义了一个“不可逆转点”,在此之后,Cdc6的合成无法促进酵母中的DNA复制。
Genes Dev. 1996 Jun 15;10(12):1516-31. doi: 10.1101/gad.10.12.1516.
7
S-phase-promoting cyclin-dependent kinases prevent re-replication by inhibiting the transition of replication origins to a pre-replicative state.S期促进细胞周期蛋白依赖性激酶通过抑制复制起点向复制前状态的转变来防止重新复制。
Curr Biol. 1995 Nov 1;5(11):1257-69. doi: 10.1016/s0960-9822(95)00252-1.
8
Among B-type cyclins only CLB5 and CLB6 promote premeiotic S phase in Saccharomyces cerevisiae.在 B 型细胞周期蛋白中,只有 CLB5 和 CLB6 能够促进酿酒酵母的减数分裂前 S 期。
Genetics. 2012 Mar;190(3):1001-16. doi: 10.1534/genetics.111.134684. Epub 2011 Dec 29.
9
Negative regulation of G1 and G2 by S-phase cyclins of Saccharomyces cerevisiae.酿酒酵母S期细胞周期蛋白对G1期和G2期的负调控。
Mol Cell Biol. 1995 Sep;15(9):5030-42. doi: 10.1128/MCB.15.9.5030.
10
Cyclin specificity in the phosphorylation of cyclin-dependent kinase substrates.细胞周期蛋白依赖性激酶底物磷酸化中的细胞周期蛋白特异性
Nature. 2005 Mar 3;434(7029):104-8. doi: 10.1038/nature03329.

引用本文的文献

1
The RNA-binding protein Puf5 and the HMGB protein Ixr1 regulate cell cycle-specific expression of CLB1 and CLB2 in Saccharomyces cerevisiae.RNA结合蛋白Puf5和高迁移率族蛋白Ixr1调节酿酒酵母中CLB1和CLB2的细胞周期特异性表达。
PLoS One. 2025 Feb 3;20(2):e0316433. doi: 10.1371/journal.pone.0316433. eCollection 2025.
2
CDK activity provides temporal and quantitative cues for organizing genome duplication.CDK 活性为基因组复制的组织提供了时间和数量上的线索。
PLoS Genet. 2018 Feb 21;14(2):e1007214. doi: 10.1371/journal.pgen.1007214. eCollection 2018 Feb.
3
Sequential phosphorylation of CST subunits by different cyclin-Cdk1 complexes orchestrate telomere replication.不同的细胞周期蛋白-Cdk1复合物对CST亚基进行顺序磷酸化,从而协调端粒复制。
Cell Cycle. 2017 Jul 3;16(13):1271-1287. doi: 10.1080/15384101.2017.1312235. Epub 2017 Jun 26.
4
Method for identifying phosphorylated substrates of specific cyclin/cyclin-dependent kinase complexes.特定细胞周期蛋白/细胞周期蛋白依赖性激酶复合物的磷酸化底物鉴定方法。
Proc Natl Acad Sci U S A. 2014 Aug 5;111(31):11323-8. doi: 10.1073/pnas.1409666111. Epub 2014 Jul 21.
5
Quantitative analysis of triple-mutant genetic interactions.三重突变体遗传相互作用的定量分析。
Nat Protoc. 2014 Aug;9(8):1867-81. doi: 10.1038/nprot.2014.127. Epub 2014 Jul 10.
6
Systematic triple-mutant analysis uncovers functional connectivity between pathways involved in chromosome regulation.系统三重突变分析揭示了参与染色体调控的途径之间的功能连接。
Cell Rep. 2013 Jun 27;3(6):2168-78. doi: 10.1016/j.celrep.2013.05.007. Epub 2013 Jun 6.
7
Molecular basis of the functional distinction between Cln1 and Cln2 cyclins.Cln1 和 Cln2 细胞周期蛋白功能差异的分子基础。
Cell Cycle. 2012 Aug 15;11(16):3117-31. doi: 10.4161/cc.21505. Epub 2012 Aug 14.
8
Among B-type cyclins only CLB5 and CLB6 promote premeiotic S phase in Saccharomyces cerevisiae.在 B 型细胞周期蛋白中,只有 CLB5 和 CLB6 能够促进酿酒酵母的减数分裂前 S 期。
Genetics. 2012 Mar;190(3):1001-16. doi: 10.1534/genetics.111.134684. Epub 2011 Dec 29.
9
Dynamics of Cdk1 substrate specificity during the cell cycle.细胞周期中 CDK1 底物特异性的动力学。
Mol Cell. 2011 Jun 10;42(5):610-23. doi: 10.1016/j.molcel.2011.05.016.
10
Candida albicans cyclin Clb4 carries S-phase cyclin activity.白色念珠菌细胞周期蛋白Clb4具有S期细胞周期蛋白活性。
Eukaryot Cell. 2010 Sep;9(9):1311-9. doi: 10.1128/EC.00038-10. Epub 2010 Jul 16.

本文引用的文献

1
Evidence that a free-running oscillator drives G1 events in the budding yeast cell cycle.有证据表明,一个自主运行的振荡器驱动芽殖酵母细胞周期中的G1期事件。
Nature. 1999 Sep 23;401(6751):394-7. doi: 10.1038/43927.
2
Specialization and targeting of B-type cyclins.
Mol Cell. 1999 Jul;4(1):11-9. doi: 10.1016/s1097-2765(00)80183-5.
3
Comprehensive identification of cell cycle-regulated genes of the yeast Saccharomyces cerevisiae by microarray hybridization.通过微阵列杂交全面鉴定酿酒酵母细胞周期调控基因。
Mol Biol Cell. 1998 Dec;9(12):3273-97. doi: 10.1091/mbc.9.12.3273.
4
CLB5-dependent activation of late replication origins in S. cerevisiae.酿酒酵母中依赖CLB5的晚期复制起点激活。
Mol Cell. 1998 Aug;2(2):173-82. doi: 10.1016/s1097-2765(00)80127-6.
5
Additional modules for versatile and economical PCR-based gene deletion and modification in Saccharomyces cerevisiae.用于酿酒酵母中基于PCR的通用且经济的基因缺失和修饰的附加模块。
Yeast. 1998 Jul;14(10):953-61. doi: 10.1002/(SICI)1097-0061(199807)14:10<953::AID-YEA293>3.0.CO;2-U.
6
Replication profile of Saccharomyces cerevisiae chromosome VI.酿酒酵母第六条染色体的复制图谱。
Genes Cells. 1997 Nov;2(11):667-78. doi: 10.1046/j.1365-2443.1997.1520350.x.
7
Flow cytometric analysis of DNA content in budding yeast.芽殖酵母DNA含量的流式细胞仪分析
Methods Enzymol. 1997;283:322-32. doi: 10.1016/s0076-6879(97)83026-1.
8
At the heart of the budding yeast cell cycle.在出芽酵母细胞周期的核心。
Trends Genet. 1996 Oct;12(10):405-12. doi: 10.1016/0168-9525(96)10041-x.
9
Multiple determinants controlling activation of yeast replication origins late in S phase.多个决定因素控制酵母复制起点在S期后期的激活。
Genes Dev. 1996 Jul 1;10(13):1595-607. doi: 10.1101/gad.10.13.1595.
10
Analysis of replication intermediates by two-dimensional agarose gel electrophoresis.通过二维琼脂糖凝胶电泳分析复制中间体。
Methods Enzymol. 1995;262:613-27. doi: 10.1016/0076-6879(95)62048-6.

酵母有丝分裂周期蛋白Clb2在复制起点激发过程中不能替代S期周期蛋白。

The yeast mitotic cyclin Clb2 cannot substitute for S phase cyclins in replication origin firing.

作者信息

Donaldson A D

机构信息

Department of Biochemistry, University of Dundee, Scotland, UK.

出版信息

EMBO Rep. 2000 Dec;1(6):507-12. doi: 10.1093/embo-reports/kvd108.

DOI:10.1093/embo-reports/kvd108
PMID:11263495
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1083780/
Abstract

Cyclin-dependent kinases (CDKs) drive the cell cycle, central to which is the accurate control of chromosome replication. In Saccharomyces cerevisiae, six closely related B-type cyclins (Clb1-6) drive the events of S phase and mitosis. Either Clb5 or Clb6 can activate early-firing replication origins, whereas only Clb5 can activate late origins. Clb1-4 are expressed later in the cell cycle. Whether Clb cyclins differ only in timing of expression, or else impart different kinase specificities is under ongoing investigation. This study shows that the expression of Clb2 during S phase in cells lacking Clb5 failed to rescue late origin activation. Early expression of Clb2 in cells lacking both Clb5 and Clb6 did not activate early origins on schedule to restore the correct S phase entry time. Therefore, Clb2 cannot drive timely activation of either early or late replication origins, demonstrating that Clb2-directed CDK has a specificity distinct from that driven by Clb5 and Clb6.

摘要

细胞周期蛋白依赖性激酶(CDK)驱动细胞周期,其中对染色体复制的精确控制至关重要。在酿酒酵母中,六种密切相关的B型细胞周期蛋白(Clb1 - 6)驱动S期和有丝分裂事件。Clb5或Clb6均可激活早期启动的复制起点,而只有Clb5能激活晚期起点。Clb1 - 4在细胞周期后期表达。Clb细胞周期蛋白是仅在表达时间上有所不同,还是具有不同的激酶特异性,仍在研究中。本研究表明,在缺乏Clb5的细胞中,S期时Clb2的表达未能挽救晚期起点激活。在同时缺乏Clb5和Clb6的细胞中,Clb2的早期表达未能按时激活早期起点以恢复正确的S期进入时间。因此,Clb2不能驱动早期或晚期复制起点的及时激活,这表明Clb2指导的CDK具有与Clb5和Clb6驱动的CDK不同的特异性。