• 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

XRCC4功能的分子遗传学特征分析。

Molecular genetic characterization of XRCC4 function.

作者信息

Mizuta R, Cheng H L, Gao Y, Alt F W

机构信息

Howard Hughes Medical Institute, Children's Hospital, Boston, MA 02115, USA.

出版信息

Int Immunol. 1997 Oct;9(10):1607-13. doi: 10.1093/intimm/9.10.1607.

DOI:10.1093/intimm/9.10.1607
PMID:9352367
Abstract

XRCC4 is a generally expressed protein of 334 amino acids that is involved in the repair of DNA double-strand breaks and in V(D)J recombination, but its function is unknown. In this study, we have used a mutational approach and the yeast two-hybrid method to perform an initial characterization of this protein. We show that the XRCC4 protein is located in the nucleus. We also demonstrate that several potential phosphorylation sites are not required for XRCC4 function in a transient V(D)J recombination assay. In addition, we show that XRCC4 forms a homodimer in vivo with the homodimerization domain being located within amino acids 115-204. Finally, we define a core domain of XRCC4 that functions in V(D)J recombination and comprises amino acids 18-204. Potential functions of XRCC4 are discussed.

摘要

XRCC4是一种普遍表达的蛋白质,由334个氨基酸组成,参与DNA双链断裂修复和V(D)J重组,但其功能尚不清楚。在本研究中,我们采用突变方法和酵母双杂交方法对该蛋白质进行了初步表征。我们发现XRCC4蛋白定位于细胞核。我们还证明,在瞬时V(D)J重组试验中,几个潜在的磷酸化位点对于XRCC4的功能并非必需。此外,我们表明XRCC4在体内形成同二聚体,同二聚化结构域位于氨基酸115 - 204内。最后,我们确定了XRCC4在V(D)J重组中发挥作用的核心结构域,该结构域由氨基酸18 - 204组成。文中还讨论了XRCC4的潜在功能。

相似文献

1
Molecular genetic characterization of XRCC4 function.XRCC4功能的分子遗传学特征分析。
Int Immunol. 1997 Oct;9(10):1607-13. doi: 10.1093/intimm/9.10.1607.
2
The XRCC4 gene encodes a novel protein involved in DNA double-strand break repair and V(D)J recombination.XRCC4基因编码一种参与DNA双链断裂修复和V(D)J重组的新型蛋白质。
Cell. 1995 Dec 29;83(7):1079-89. doi: 10.1016/0092-8674(95)90135-3.
3
DNA binding of Xrcc4 protein is associated with V(D)J recombination but not with stimulation of DNA ligase IV activity.Xrcc4蛋白与DNA的结合与V(D)J重组相关,但与DNA连接酶IV活性的刺激无关。
EMBO J. 1999 Apr 1;18(7):2008-18. doi: 10.1093/emboj/18.7.2008.
4
V(D)J recombination intermediates and non-standard products in XRCC4-deficient cells.XRCC4缺陷细胞中的V(D)J重组中间体和非标准产物。
Nucleic Acids Res. 1998 Aug 15;26(16):3769-75. doi: 10.1093/nar/26.16.3769.
5
Crystal structure of the Xrcc4 DNA repair protein and implications for end joining.Xrcc4 DNA修复蛋白的晶体结构及其对末端连接的影响。
EMBO J. 2000 Nov 15;19(22):5962-70. doi: 10.1093/emboj/19.22.5962.
6
Requirement for an interaction of XRCC4 with DNA ligase IV for wild-type V(D)J recombination and DNA double-strand break repair in vivo.体内野生型V(D)J重组和DNA双链断裂修复中XRCC4与DNA连接酶IV相互作用的要求。
J Biol Chem. 1998 Sep 18;273(38):24708-14. doi: 10.1074/jbc.273.38.24708.
7
Saccharomyces cerevisiae LIF1: a function involved in DNA double-strand break repair related to mammalian XRCC4.酿酒酵母LIF1:一种与哺乳动物XRCC4相关的参与DNA双链断裂修复的功能。
EMBO J. 1998 Jul 15;17(14):4188-98. doi: 10.1093/emboj/17.14.4188.
8
Activity of DNA ligase IV stimulated by complex formation with XRCC4 protein in mammalian cells.在哺乳动物细胞中,与XRCC4蛋白形成复合物刺激DNA连接酶IV的活性。
Nature. 1997 Jul 31;388(6641):492-5. doi: 10.1038/41358.
9
Asparagine 326 in the extremely C-terminal region of XRCC4 is essential for the cell survival after irradiation.XRCC4极端C末端区域的天冬酰胺326对于辐射后的细胞存活至关重要。
Biochem Biophys Res Commun. 2015 Feb 20;457(4):526-31. doi: 10.1016/j.bbrc.2015.01.015. Epub 2015 Jan 15.
10
An xrcc4 defect or Wortmannin stimulates homologous recombination specifically induced by double-strand breaks in mammalian cells.Xrcc4缺陷或渥曼青霉素可刺激哺乳动物细胞中由双链断裂特异性诱导的同源重组。
Nucleic Acids Res. 2002 Aug 1;30(15):3454-63. doi: 10.1093/nar/gkf452.

引用本文的文献

1
Specific Roles of XRCC4 Paralogs PAXX and XLF during V(D)J Recombination.XRCC4旁系同源物PAXX和XLF在V(D)J重组过程中的特定作用。
Cell Rep. 2016 Sep 13;16(11):2967-2979. doi: 10.1016/j.celrep.2016.08.069. Epub 2016 Sep 2.
2
Ionizing radiation-induced XRCC4 phosphorylation is mediated through ATM in addition to DNA-PK.除DNA-PK外,电离辐射诱导的XRCC4磷酸化还通过ATM介导。
Proc Jpn Acad Ser B Phys Biol Sci. 2014;90(9):365-72. doi: 10.2183/pjab.90.365.
3
Interaction of DNA repair gene polymorphisms and aflatoxin B1 in the risk of hepatocellular carcinoma.
DNA修复基因多态性与黄曲霉毒素B1在肝细胞癌风险中的相互作用。
Int J Clin Exp Pathol. 2014 Aug 15;7(9):6231-44. eCollection 2014.
4
Normal Sequence and Activity but Reduced Levels of DNA-Pkcs in Human Lymphoblastic Cells Implicate Impaired Protein Stability with Radiosensitive Phenotype.人类淋巴细胞中DNA-Pkcs水平降低但序列和活性正常,提示蛋白质稳定性受损并伴有放射敏感表型。
J Cancer. 2013 Sep 7;4(8):606-13. doi: 10.7150/jca.6453.
5
Ancient and recent adaptive evolution of primate non-homologous end joining genes.灵长类非同源末端连接基因的古老和近期适应性进化。
PLoS Genet. 2010 Oct 21;6(10):e1001169. doi: 10.1371/journal.pgen.1001169.
6
Structural biology of DNA repair: spatial organisation of the multicomponent complexes of nonhomologous end joining.DNA修复的结构生物学:非同源末端连接多组分复合物的空间组织
J Nucleic Acids. 2010 Aug 25;2010:621695. doi: 10.4061/2010/621695.
7
Loss of DNA ligase IV prevents recognition of DNA by double-strand break repair proteins XRCC4 and XLF.DNA连接酶IV的缺失会阻止双链断裂修复蛋白XRCC4和XLF对DNA的识别。
Nucleic Acids Res. 2008 Oct;36(18):5773-86. doi: 10.1093/nar/gkn552. Epub 2008 Sep 9.
8
SUMO modification of human XRCC4 regulates its localization and function in DNA double-strand break repair.人类XRCC4的SUMO修饰调节其在DNA双链断裂修复中的定位和功能。
Mol Cell Biol. 2006 Mar;26(5):1786-94. doi: 10.1128/MCB.26.5.1786-1794.2006.
9
Crystal structure of the Xrcc4 DNA repair protein and implications for end joining.Xrcc4 DNA修复蛋白的晶体结构及其对末端连接的影响。
EMBO J. 2000 Nov 15;19(22):5962-70. doi: 10.1093/emboj/19.22.5962.
10
Ku recruits the XRCC4-ligase IV complex to DNA ends.Ku将XRCC4-连接酶IV复合物招募至DNA末端。
Mol Cell Biol. 2000 May;20(9):2996-3003. doi: 10.1128/MCB.20.9.2996-3003.2000.