• 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
NDT80 and the meiotic recombination checkpoint regulate expression of middle sporulation-specific genes in Saccharomyces cerevisiae.NDT80和减数分裂重组检查点调节酿酒酵母中孢子形成中期特异性基因的表达。
Mol Cell Biol. 1998 Oct;18(10):5750-61. doi: 10.1128/MCB.18.10.5750.
2
Role of Ndt80, Sum1, and Swe1 as targets of the meiotic recombination checkpoint that control exit from pachytene and spore formation in Saccharomyces cerevisiae.Ndt80、Sum1和Swe1作为减数分裂重组检查点的靶点在酿酒酵母中控制粗线期退出和孢子形成的作用。
Mol Cell Biol. 2002 Sep;22(18):6430-40. doi: 10.1128/MCB.22.18.6430-6440.2002.
3
The pachytene checkpoint in Saccharomyces cerevisiae requires the Sum1 transcriptional repressor.酿酒酵母中的粗线期检查点需要Sum1转录抑制因子。
EMBO J. 2000 Dec 1;19(23):6489-97. doi: 10.1093/emboj/19.23.6489.
4
Phosphorylation and maximal activity of Saccharomyces cerevisiae meiosis-specific transcription factor Ndt80 is dependent on Ime2.酿酒酵母减数分裂特异性转录因子Ndt80的磷酸化和最大活性依赖于Ime2。
Mol Cell Biol. 2002 Oct;22(20):7024-40. doi: 10.1128/MCB.22.20.7024-7040.2002.
5
Gametogenesis in yeast is regulated by a transcriptional cascade dependent on Ndt80.酵母中的配子发生受依赖于Ndt80的转录级联调控。
Mol Cell. 1998 Apr;1(5):685-96. doi: 10.1016/s1097-2765(00)80068-4.
6
Saccharomyces cerevisiae checkpoint genes MEC1, RAD17 and RAD24 are required for normal meiotic recombination partner choice.酿酒酵母检查点基因MEC1、RAD17和RAD24是正常减数分裂重组伴侣选择所必需的。
Genetics. 1999 Oct;153(2):607-20. doi: 10.1093/genetics/153.2.607.
7
The Sum1/Ndt80 transcriptional switch and commitment to meiosis in Saccharomyces cerevisiae.酿酒酵母中 Sum1/Ndt80 转录开关和减数分裂的决定。
Microbiol Mol Biol Rev. 2012 Mar;76(1):1-15. doi: 10.1128/MMBR.05010-11.
8
Regulation of the premiddle and middle phases of expression of the NDT80 gene during sporulation of Saccharomyces cerevisiae.酿酒酵母孢子形成过程中NDT80基因表达前期和中期的调控
Mol Cell Biol. 2002 Sep;22(18):6417-29. doi: 10.1128/MCB.22.18.6417-6429.2002.
9
Meiosis: step-by-step through sporulation.减数分裂:通过孢子形成的逐步过程。
Curr Biol. 1998 Jun 18;8(13):R461-3. doi: 10.1016/s0960-9822(98)70293-3.
10
Activity of phosphoforms and truncated versions of Ndt80, a checkpoint-regulated sporulation-specific transcription factor of Saccharomyces cerevisiae.酿酒酵母中Ndt80(一种检查点调节的孢子形成特异性转录因子)的磷酸化形式和截短版本的活性。
Mol Genet Genomics. 2003 Dec;270(4):324-36. doi: 10.1007/s00438-003-0922-3. Epub 2003 Nov 7.

引用本文的文献

1
A Conserved Disruption of the Nuclear Permeability Barrier in Meiosis is Controlled by a Kinase-Phosphatase Pair in .减数分裂中核渗透屏障的保守破坏由一对激酶-磷酸酶控制。
bioRxiv. 2025 May 15:2025.05.14.654091. doi: 10.1101/2025.05.14.654091.
2
Membrane and organelle rearrangement during ascospore formation in budding yeast.出芽酵母中分生孢子形成过程中的膜和细胞器重排。
Microbiol Mol Biol Rev. 2024 Sep 26;88(3):e0001324. doi: 10.1128/mmbr.00013-24. Epub 2024 Jun 20.
3
Meiotic prophase length modulates Tel1-dependent DNA double-strand break interference.减数分裂前期长度调节 Tel1 依赖性 DNA 双链断裂干扰。
PLoS Genet. 2024 Mar 1;20(3):e1011140. doi: 10.1371/journal.pgen.1011140. eCollection 2024 Mar.
4
Spo13/MEIKIN ensures a Two-Division meiosis by preventing the activation of APC/C at meiosis I.Spo13/MEIKIN 通过防止 APC/C 在减数分裂 I 中激活来确保二分裂减数分裂。
EMBO J. 2023 Oct 16;42(20):e114288. doi: 10.15252/embj.2023114288. Epub 2023 Sep 20.
5
Conservation and Expansion of Transcriptional Factor Repertoire in the Species Complex.物种复合体中转录因子库的保守与扩展
J Fungi (Basel). 2023 Mar 15;9(3):359. doi: 10.3390/jof9030359.
6
Conservation and Expansion of Transcriptional Factor Repertoire in the Species Complex.物种复合体中转录因子库的保守与扩展
bioRxiv. 2023 Feb 10:2023.02.09.527873. doi: 10.1101/2023.02.09.527873.
7
High-throughput genetic screening of meiotic commitment using fluorescence microscopy in .使用荧光显微镜进行减数分裂承诺的高通量遗传筛选。
STAR Protoc. 2022 Oct 27;3(4):101797. doi: 10.1016/j.xpro.2022.101797. eCollection 2022 Dec 16.
8
Transcription Factor Negatively Regulates Conidiation by Affecting Utilization of Carbon and Nitrogen Source in .转录因子通过影响……中碳源和氮源的利用对分生孢子形成起负调控作用。
J Fungi (Basel). 2022 Jun 1;8(6):594. doi: 10.3390/jof8060594.
9
Identification of 14-3-3 proteins, Polo kinase, and RNA-binding protein Pes4 as key regulators of meiotic commitment in budding yeast.鉴定出 14-3-3 蛋白、Polo 激酶和 RNA 结合蛋白 Pes4 是芽殖酵母减数分裂起始的关键调节因子。
Curr Biol. 2022 Apr 11;32(7):1534-1547.e9. doi: 10.1016/j.cub.2022.02.022. Epub 2022 Mar 2.
10
Distinct requirements for the COMPASS core subunits Set1, Swd1, and Swd3 during meiosis in the budding yeast Saccharomyces cerevisiae.在酿酒酵母有丝分裂过程中,COMPASS 核心亚基 Set1、Swd1 和 Swd3 有不同的需求。
G3 (Bethesda). 2021 Oct 19;11(11). doi: 10.1093/g3journal/jkab283.

本文引用的文献

1
Gametogenesis in yeast is regulated by a transcriptional cascade dependent on Ndt80.酵母中的配子发生受依赖于Ndt80的转录级联调控。
Mol Cell. 1998 Apr;1(5):685-96. doi: 10.1016/s1097-2765(00)80068-4.
2
Transcriptional repression by UME6 involves deacetylation of lysine 5 of histone H4 by RPD3.UME6介导的转录抑制作用涉及RPD3对组蛋白H4赖氨酸5位的去乙酰化过程。
Nature. 1998 Apr 23;392(6678):831-5. doi: 10.1038/33952.
3
The Schizosaccharomyces pombe mei4+ gene encodes a meiosis-specific transcription factor containing a forkhead DNA-binding domain.粟酒裂殖酵母mei4+基因编码一种含有叉头DNA结合结构域的减数分裂特异性转录因子。
Mol Cell Biol. 1998 Apr;18(4):2118-29. doi: 10.1128/MCB.18.4.2118.
4
Histone deacetylase activity of Rpd3 is important for transcriptional repression in vivo.Rpd3的组蛋白去乙酰化酶活性对于体内转录抑制很重要。
Genes Dev. 1998 Mar 15;12(6):797-805. doi: 10.1101/gad.12.6.797.
5
Histone acetylation and transcriptional regulatory mechanisms.组蛋白乙酰化与转录调控机制。
Genes Dev. 1998 Mar 1;12(5):599-606. doi: 10.1101/gad.12.5.599.
6
Prospore membrane formation defines a developmentally regulated branch of the secretory pathway in yeast.芽孢膜的形成定义了酵母分泌途径中一个受发育调控的分支。
J Cell Biol. 1998 Jan 12;140(1):29-37. doi: 10.1083/jcb.140.1.29.
7
Interaction of yeast repressor-activator protein Ume6p with glycogen synthase kinase 3 homolog Rim11p.酵母阻遏物-激活蛋白Ume6p与糖原合酶激酶3同源物Rim11p的相互作用。
Mol Cell Biol. 1997 Dec;17(12):7230-6. doi: 10.1128/MCB.17.12.7230.
8
A large protein complex containing the yeast Sin3p and Rpd3p transcriptional regulators.一种包含酵母Sin3p和Rpd3p转录调节因子的大型蛋白质复合物。
Mol Cell Biol. 1997 Aug;17(8):4852-8. doi: 10.1128/MCB.17.8.4852.
9
Mutations in Saccharomyces cerevisiae that block meiotic prophase chromosome metabolism and confer cell cycle arrest at pachytene identify two new meiosis-specific genes SAE1 and SAE3.酿酒酵母中阻断减数分裂前期染色体代谢并使细胞周期在粗线期停滞的突变,鉴定出两个新的减数分裂特异性基因SAE1和SAE3。
Genetics. 1997 Jul;146(3):817-34. doi: 10.1093/genetics/146.3.817.
10
A general method for identifying recessive diploid-specific mutations in Saccharomyces cerevisiae, its application to the isolation of mutants blocked at intermediate stages of meiotic prophase and characterization of a new gene SAE2.一种鉴定酿酒酵母中隐性二倍体特异性突变的通用方法,其在分离减数分裂前期中间阶段受阻突变体中的应用以及新基因SAE2的表征
Genetics. 1997 Jul;146(3):797-816. doi: 10.1093/genetics/146.3.797.

NDT80和减数分裂重组检查点调节酿酒酵母中孢子形成中期特异性基因的表达。

NDT80 and the meiotic recombination checkpoint regulate expression of middle sporulation-specific genes in Saccharomyces cerevisiae.

作者信息

Hepworth S R, Friesen H, Segall J

机构信息

Department of Biochemistry, University of Toronto, Toronto, Ontario, Canada M5S 1A8.

出版信息

Mol Cell Biol. 1998 Oct;18(10):5750-61. doi: 10.1128/MCB.18.10.5750.

DOI:10.1128/MCB.18.10.5750
PMID:9742092
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC109161/
Abstract

Distinct classes of sporulation-specific genes are sequentially expressed during the process of spore formation in Saccharomyces cerevisiae. The transition from expression of early meiotic genes to expression of middle sporulation-specific genes occurs at about the time that cells exit from pachytene and form the meiosis I spindle. To identify genes encoding potential regulators of middle sporulation-specific gene expression, we screened for mutants that expressed early meiotic genes but failed to express middle sporulation-specific genes. We identified mutant alleles of RPD3, SIN3, and NDT80 in this screen. Rpd3p, a histone deacetylase, and Sin3p are global modulators of gene expression. Ndt80p promotes entry into the meiotic divisions. We found that entry into the meiotic divisions was not required for activation of middle sporulation genes; these genes were efficiently expressed in a clb1 clb3 clb4 strain, which fails to enter the meiotic divisions due to reduced Clb-dependent activation of Cdc28p kinase. In contrast, middle sporulation genes were not expressed in a dmc1 strain, which fails to enter the meiotic divisions because a defect in meiotic recombination leads to a RAD17-dependent checkpoint arrest. Expression of middle sporulation genes, as well as entry into the meiotic divisions, was restored to a dmc1 strain by mutation of RAD17. Our studies also revealed that NDT80 was a temporally distinct, pre-middle sporulation gene and that its expression was reduced, but not abolished, on mutation of DMC1, RPD3, SIN3, or NDT80 itself. In summary, our data indicate that Ndt80p is required for expression of middle sporulation genes and that the activity of Ndt80p is controlled by the meiotic recombination checkpoint. Thus, middle genes are expressed only on completion of meiotic recombination and subsequent generation of an active form of Ndt80p.

摘要

在酿酒酵母的孢子形成过程中,不同类别的孢子形成特异性基因会被顺序表达。从早期减数分裂基因的表达过渡到中期孢子形成特异性基因的表达,大约发生在细胞离开粗线期并形成减数分裂I纺锤体的时候。为了鉴定编码中期孢子形成特异性基因表达潜在调节因子的基因,我们筛选了那些表达早期减数分裂基因但未能表达中期孢子形成特异性基因的突变体。在这个筛选过程中,我们鉴定出了RPD3、SIN3和NDT80的突变等位基因。Rpd3p是一种组蛋白去乙酰化酶,Sin3p是基因表达的全局调节因子。Ndt80p促进进入减数分裂。我们发现,进入减数分裂对于中期孢子形成基因的激活并非必需;这些基因在clb1 clb3 clb4菌株中能有效表达,该菌株由于Cdc28p激酶的Clb依赖性激活降低而无法进入减数分裂。相比之下,中期孢子形成基因在dmc1菌株中不表达,该菌株由于减数分裂重组缺陷导致RAD17依赖性检查点停滞而无法进入减数分裂。通过RAD17突变,dmc1菌株恢复了中期孢子形成基因的表达以及进入减数分裂的能力。我们的研究还表明,NDT80是一个时间上不同的、孢子形成前期的基因,并且在DMC1、RPD3、SIN3或NDT80自身发生突变时,其表达会降低但不会被消除。总之,我们的数据表明Ndt80p是中期孢子形成基因表达所必需的,并且Ndt80p的活性受减数分裂重组检查点的控制。因此,只有在减数分裂重组完成并随后产生活性形式的Ndt80p后,中期基因才会表达。