• 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

GTBP, a 160-kilodalton protein essential for mismatch-binding activity in human cells.

作者信息

Palombo F, Gallinari P, Iaccarino I, Lettieri T, Hughes M, D'Arrigo A, Truong O, Hsuan J J, Jiricny J

机构信息

Istituto di Ricerche di Biologia Molecolare P. Angeletti, Pomezia, Italy.

出版信息

Science. 1995 Jun 30;268(5219):1912-4. doi: 10.1126/science.7604265.

DOI:10.1126/science.7604265
PMID:7604265
Abstract

DNA mismatch recognition and binding in human cells has been thought to be mediated by the hMSH2 protein. Here it is shown that the mismatch-binding factor consists of two distinct proteins, the 100-kilodalton hMSH2 and a 160-kilodalton polypeptide, GTBP (for G/T binding protein). Sequence analysis identified GTBP as a new member of the MutS homolog family. Both proteins are required for mismatch-specific binding, a result consistent with the finding that tumor-derived cell lines devoid of either protein are also devoid of mismatch-binding activity.

摘要

相似文献

1
GTBP, a 160-kilodalton protein essential for mismatch-binding activity in human cells.
Science. 1995 Jun 30;268(5219):1912-4. doi: 10.1126/science.7604265.
2
Isolation of an hMSH2-p160 heterodimer that restores DNA mismatch repair to tumor cells.一种能将DNA错配修复功能恢复至肿瘤细胞的hMSH2-p160异二聚体的分离。
Science. 1995 Jun 30;268(5219):1909-12. doi: 10.1126/science.7604264.
3
Appropriate partners make good matches.合适的伴侣成就美满的婚姻。
Science. 1995 Jun 30;268(5219):1857-8. doi: 10.1126/science.7604258.
4
hMutSbeta, a heterodimer of hMSH2 and hMSH3, binds to insertion/deletion loops in DNA.hMutSβ是hMSH2和hMSH3的异源二聚体,可与DNA中的插入/缺失环结合。
Curr Biol. 1996 Sep 1;6(9):1181-4. doi: 10.1016/s0960-9822(02)70685-4.
5
Mutations of GTBP in genetically unstable cells.基因不稳定细胞中GTBP的突变。
Science. 1995 Jun 30;268(5219):1915-7. doi: 10.1126/science.7604266.
6
DNA loop repair by human cell extracts.
Science. 1994 Nov 4;266(5186):814-6. doi: 10.1126/science.7973637.
7
hMSH2-independent DNA mismatch recognition by human proteins.人类蛋白质对hMSH2非依赖性DNA错配的识别
J Biol Chem. 1996 Jan 19;271(3):1789-96. doi: 10.1074/jbc.271.3.1789.
8
Construction and characterization of mismatch-containing circular DNA molecules competent for assessment of nick-directed human mismatch repair in vitro.用于体外评估切口导向的人类错配修复的含错配环状DNA分子的构建与表征。
Nucleic Acids Res. 2002 Feb 1;30(3):E14. doi: 10.1093/nar/30.3.e14.
9
Alternative splicing of GTBP in normal human tissues.
DNA Res. 1997 Oct 31;4(5):359-62. doi: 10.1093/dnares/4.5.359.
10
hMSH2 and hMSH6 play distinct roles in mismatch binding and contribute differently to the ATPase activity of hMutSalpha.人源错配修复蛋白hMSH2和hMSH6在错配结合中发挥不同作用,对人源错配修复蛋白hMutSα的ATP酶活性贡献也不同。
EMBO J. 1998 May 1;17(9):2677-86. doi: 10.1093/emboj/17.9.2677.

引用本文的文献

1
Prime Editing: Mechanistic Insights and DNA Repair Modulation.碱基编辑:作用机制洞察与DNA修复调控
Cells. 2025 Feb 13;14(4):277. doi: 10.3390/cells14040277.
2
MutLα suppresses error-prone DNA mismatch repair and preferentially protects noncoding DNA from mutations.MutLα 抑制易错 DNA 错配修复,并优先保护非编码 DNA 免受突变。
J Biol Chem. 2024 Jun;300(6):107406. doi: 10.1016/j.jbc.2024.107406. Epub 2024 May 21.
3
MutLα suppresses error-prone DNA mismatch repair and preferentially protects noncoding DNA from mutations.
MutLα抑制易出错的DNA错配修复,并优先保护非编码DNA免受突变。
bioRxiv. 2024 Apr 2:2024.04.01.587563. doi: 10.1101/2024.04.01.587563.
4
Mismatch Repair system protein deficiency as a resistance factor for locally advanced rectal adenocarcinoma patients receiving neoadjuvant chemo-radiotherapy.错配修复系统蛋白缺陷作为接受新辅助放化疗的局部晚期直肠腺癌患者的耐药因素。
Br J Cancer. 2023 Nov;129(10):1619-1624. doi: 10.1038/s41416-023-02444-2. Epub 2023 Sep 25.
5
MutSα and MutSβ as size-dependent cellular determinants for prime editing in human embryonic stem cells.MutSα和MutSβ作为人类胚胎干细胞中碱基编辑的大小依赖性细胞决定因素。
Mol Ther Nucleic Acids. 2023 May 18;32:914-922. doi: 10.1016/j.omtn.2023.05.015. eCollection 2023 Jun 13.
6
A conserved motif in the disordered linker of human MLH1 is vital for DNA mismatch repair and its function is diminished by a cancer family mutation.人类 MLH1 无规则连接区的一个保守模体对于 DNA 错配修复至关重要,而一个癌症家族突变则削弱了其功能。
Nucleic Acids Res. 2023 Jul 7;51(12):6307-6320. doi: 10.1093/nar/gkad418.
7
B cell class switch recombination is regulated by DYRK1A through MSH6 phosphorylation.B 细胞类别转换重组受 DYRK1A 通过 MSH6 磷酸化调节。
Nat Commun. 2023 Mar 16;14(1):1462. doi: 10.1038/s41467-023-37205-5.
8
DNA Damage Response Alterations in Ovarian Cancer: From Molecular Mechanisms to Therapeutic Opportunities.卵巢癌中的DNA损伤反应改变:从分子机制到治疗机遇
Cancers (Basel). 2023 Jan 10;15(2):448. doi: 10.3390/cancers15020448.
9
Mismatch repair is a double-edged sword in the battle against microsatellite instability.错配修复是对抗微卫星不稳定的双刃剑。
Expert Rev Mol Med. 2022 Sep 5;24:e32. doi: 10.1017/erm.2022.16.
10
The impact of rare germline variants on human somatic mutation processes.罕见种系变异对人类体细胞突变过程的影响。
Nat Commun. 2022 Jun 28;13(1):3724. doi: 10.1038/s41467-022-31483-1.