• 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

HOP1基因编码酵母染色体中一种减数分裂特异性成分。

The HOP1 gene encodes a meiosis-specific component of yeast chromosomes.

作者信息

Hollingsworth N M, Goetsch L, Byers B

机构信息

Department of Genetics, University of Washington, Seattle 98195.

出版信息

Cell. 1990 Apr 6;61(1):73-84. doi: 10.1016/0092-8674(90)90216-2.

DOI:10.1016/0092-8674(90)90216-2
PMID:2107981
Abstract

The HOP1 gene in Saccharomyces cerevisiae is important for meiotic chromosomal pairing, because hop1 diploids fail to form synaptonemal complex during meiosis and are defective in crossing over between, but not within, chromosomes. We demonstrate here that the HOP1 gene is transcriptionally regulated during sporulation and that the HOP1 protein is situated along the lengths of meiotic chromosomes. Furthermore, the HOP1 protein contains a Cys2/Cys2 zinc finger motif. A mutation within this motif that changes a cysteine to serine results in the hop1 phenotype, consistent with the possibility that the HOP1 gene product acts in chromosome synapsis by directly interacting with DNA. These observations demonstrate that HOP1 encodes a component of meiotic chromosomes, perhaps serving as a constituent of the synaptonemal complex.

摘要

酿酒酵母中的HOP1基因对减数分裂染色体配对很重要,因为hop1二倍体在减数分裂过程中无法形成联会复合体,并且在染色体之间而非染色体内的交叉互换存在缺陷。我们在此证明,HOP1基因在孢子形成过程中受到转录调控,并且HOP1蛋白沿减数分裂染色体的长度分布。此外,HOP1蛋白包含一个Cys2/Cys2锌指基序。该基序内将一个半胱氨酸突变为丝氨酸的突变会导致hop1表型,这与HOP1基因产物通过直接与DNA相互作用参与染色体联会的可能性一致。这些观察结果表明,HOP1编码减数分裂染色体的一个组分,可能作为联会复合体的一个组成部分。

相似文献

1
The HOP1 gene encodes a meiosis-specific component of yeast chromosomes.HOP1基因编码酵母染色体中一种减数分裂特异性成分。
Cell. 1990 Apr 6;61(1):73-84. doi: 10.1016/0092-8674(90)90216-2.
2
HOP1: a yeast meiotic pairing gene.HOP1:一种酵母减数分裂配对基因。
Genetics. 1989 Mar;121(3):445-62. doi: 10.1093/genetics/121.3.445.
3
A conditional allele of the Saccharomyces cerevisiae HOP1 gene is suppressed by overexpression of two other meiosis-specific genes: RED1 and REC104.酿酒酵母HOP1基因的一个条件等位基因被另外两个减数分裂特异性基因RED1和REC104的过表达所抑制。
Genetics. 1993 Apr;133(4):785-97. doi: 10.1093/genetics/133.4.785.
4
Insertional mutations in the yeast HOP1 gene: evidence for multimeric assembly in meiosis.酵母HOP1基因中的插入突变:减数分裂中多聚体组装的证据。
Genetics. 1994 Feb;136(2):449-64. doi: 10.1093/genetics/136.2.449.
5
A DNA binding factor (UBF) interacts with a positive regulatory element in the promoters of genes expressed during meiosis and vegetative growth in yeast.一种DNA结合因子(UBF)与酵母减数分裂和营养生长过程中表达的基因启动子中的正调控元件相互作用。
Nucleic Acids Res. 1995 Sep 11;23(17):3449-56. doi: 10.1093/nar/23.17.3449.
6
The yeast Red1 protein localizes to the cores of meiotic chromosomes.酵母Red1蛋白定位于减数分裂染色体的核心部位。
J Cell Biol. 1997 Mar 10;136(5):957-67. doi: 10.1083/jcb.136.5.957.
7
Saccharomyces cerevisiae Hop1 zinc finger motif is the minimal region required for its function in vitro.酿酒酵母Hop1锌指基序是其体外功能所需的最小区域。
J Biol Chem. 2004 Jul 9;279(28):28961-9. doi: 10.1074/jbc.M403727200. Epub 2004 Apr 28.
8
DNA-binding activities of Hop1 protein, a synaptonemal complex component from Saccharomyces cerevisiae.霍普1蛋白的DNA结合活性,一种来自酿酒酵母的联会复合体成分。
Mol Cell Biol. 1998 Mar;18(3):1424-35. doi: 10.1128/MCB.18.3.1424.
9
Saccharomyces cerevisiae Hop1 protein zinc finger motif binds to the Holliday junction and distorts the DNA structure: implications for holliday junction migration.酿酒酵母Hop1蛋白锌指基序与霍利迪连接体结合并扭曲DNA结构:对霍利迪连接体迁移的影响
Biochemistry. 2007 Nov 6;46(44):12530-42. doi: 10.1021/bi701078v. Epub 2007 Oct 13.
10
Meiotic induction of the yeast HOP1 gene is controlled by positive and negative regulatory sites.
Mol Cell Biol. 1992 Sep;12(9):3706-14. doi: 10.1128/mcb.12.9.3706-3714.1992.

引用本文的文献

1
The ATPase activity of yeast chromosome axis protein Hop1 affects the frequency of meiotic crossovers.酵母染色体轴蛋白Hop1的ATP酶活性影响减数分裂交叉的频率。
Nucleic Acids Res. 2025 Jan 24;53(3). doi: 10.1093/nar/gkae1264.
2
ASYNAPSIS3 has diverse dosage-dependent effects on meiotic crossover formation in Brassica napus.ASYNAPSIS3 在甘蓝型油菜减数分裂交叉形成中具有多种剂量依赖性效应。
Plant Cell. 2024 Sep 3;36(9):3838-3856. doi: 10.1093/plcell/koae207.
3
Canonical and noncanonical roles of Hop1 are crucial for meiotic prophase in the fungus Sordaria macrospora.
Hop1 的规范和非规范作用对真菌大孢子菌减数分裂前期至关重要。
PLoS Biol. 2024 Jul 1;22(7):e3002705. doi: 10.1371/journal.pbio.3002705. eCollection 2024 Jul.
4
Meiosis through three centuries.减数分裂的三个世纪。
Chromosoma. 2024 Apr;133(2):93-115. doi: 10.1007/s00412-024-00822-0.
5
Replication protein-A, RPA, plays a pivotal role in the maintenance of recombination checkpoint in yeast meiosis.复制蛋白A(RPA)在酵母减数分裂中重组检查点的维持中起关键作用。
Sci Rep. 2024 Apr 25;14(1):9550. doi: 10.1038/s41598-024-60082-x.
6
Absence of chromosome axis protein recruitment prevents meiotic recombination chromosome-wide in the budding yeast .染色体轴蛋白募集的缺失阻止了芽殖酵母减数分裂过程中染色体的广泛重组。
Proc Natl Acad Sci U S A. 2024 Mar 19;121(12):e2312820121. doi: 10.1073/pnas.2312820121. Epub 2024 Mar 13.
7
Physical interaction with Spo11 mediates the localisation of Mre11 to chromatin in meiosis and promotes its nuclease activity.与 Spo11 的物理相互作用将 Mre11 定位于减数分裂中的染色质,并促进其核酸酶活性。
Nucleic Acids Res. 2024 May 8;52(8):4328-4343. doi: 10.1093/nar/gkae111.
8
The N-terminal modification of HORMAD2 causes its ectopic persistence on synapsed chromosomes without meiotic blockade.HORMAD2 的 N 端修饰导致其在联会染色体上的异位持续存在,而没有减数分裂阻滞。
Reproduction. 2024 Mar 13;167(4). doi: 10.1530/REP-23-0330. Print 2024 Apr 1.
9
Chromatin binding by HORMAD proteins regulates meiotic recombination initiation.HORMAD 蛋白与染色质的结合调控减数分裂重组起始。
EMBO J. 2024 Mar;43(5):836-867. doi: 10.1038/s44318-024-00034-3. Epub 2024 Feb 8.
10
Exportin-mediated nucleocytoplasmic transport maintains Pch2 homeostasis during meiosis.导出蛋白介导的核质转运在减数分裂过程中维持 Pch2 的细胞内平衡。
PLoS Genet. 2023 Nov 10;19(11):e1011026. doi: 10.1371/journal.pgen.1011026. eCollection 2023 Nov.