• 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

用着色性干皮病和正常组蛋白重构的核小体的定位

Positioning of nucleosomes reconstituted with xeroderma pigmentosum and normal histones.

作者信息

Kaysen J H, Amari N M, Lambert M W

出版信息

Cell Biol Int Rep. 1987 Feb;11(2):95-101. doi: 10.1016/0309-1651(87)90109-3.

DOI:10.1016/0309-1651(87)90109-3
PMID:3030571
Abstract

Positioning of nucleosomes was examined in a reconstituted system using a plasmid DNA and histones from normal human and xeroderma pigmentosum, complementation group A (XPA), lymphoblastoid cells. The present studies indicate that the arrangement of nucleosomes, composed of normal human histones, in a region near the SV40 origin of replication on the plasmid DNA, is nonrandom. The alignment of nucleosomes in this region was not affected by the presence of histone H1. No difference in nucleosome positioning was observed when the nucleosomes were composed of histones from XPA cells.

摘要

使用来自正常人及着色性干皮病A组(XPA)淋巴母细胞样细胞的质粒DNA和组蛋白,在一个重组系统中检测核小体的定位。目前的研究表明,由正常人组蛋白组成的核小体在质粒DNA上SV40复制起点附近区域的排列是非随机的。该区域核小体的排列不受组蛋白H1存在的影响。当核小体由XPA细胞的组蛋白组成时,未观察到核小体定位有差异。

相似文献

1
Positioning of nucleosomes reconstituted with xeroderma pigmentosum and normal histones.用着色性干皮病和正常组蛋白重构的核小体的定位
Cell Biol Int Rep. 1987 Feb;11(2):95-101. doi: 10.1016/0309-1651(87)90109-3.
2
Chromatin-associated DNA endonucleases from xeroderma pigmentosum cells are defective in interaction with damaged nucleosomal DNA.来自着色性干皮病细胞的染色质相关DNA内切核酸酶在与受损核小体DNA的相互作用中存在缺陷。
Mutat Res. 1990 Mar;235(2):65-80. doi: 10.1016/0921-8777(90)90059-e.
3
Enhancement of two apurinic/apyrimidinic endonuclease activities from normal but not xeroderma pigmentosum lymphoblastoid cells by nucleosome structure.
Mutat Res. 1986 May;165(3):221-31. doi: 10.1016/0167-8817(86)90057-x.
4
Xeroderma pigmentosum endonuclease complexes show reduced activity on and affinity for psoralen cross-linked nucleosomal DNA.
Mutat Res. 1992 Mar;273(2):157-70. doi: 10.1016/0921-8777(92)90077-g.
5
Nucleosome positioning as a critical determinant for the DNA cleavage sites of mammalian DNA topoisomerase II in reconstituted simian virus 40 chromatin.核小体定位作为重组猴病毒40染色质中哺乳动物DNA拓扑异构酶II的DNA切割位点的关键决定因素。
Nucleic Acids Res. 1990 Aug 11;18(15):4553-9. doi: 10.1093/nar/18.15.4553.
6
Phasing of nucleosomes in SV40 chromatin reconstituted in vitro.体外重构的SV40染色质中核小体的相位分析。
J Biochem. 1981 May;89(5):1375-89. doi: 10.1093/oxfordjournals.jbchem.a133329.
7
Unique positioning of reconstituted nucleosomes occurs in one region of simian virus 40 DNA.重组核小体的独特定位出现在猿猴病毒40 DNA的一个区域中。
J Biol Chem. 1987 Mar 15;262(8):3872-9.
8
Immortalization of xeroderma pigmentosum cells by simian virus 40 DNA having a defective origin of DNA replication.通过具有缺陷性DNA复制起点的猿猴病毒40 DNA使着色性干皮病细胞永生化。
Somat Cell Mol Genet. 1986 Jan;12(1):13-20. doi: 10.1007/BF01560723.
9
Biological and biochemical characterization of an SV40-transformed xeroderma pigmentosum cell line.一种经SV40转化的着色性干皮病细胞系的生物学和生化特性
Exp Cell Res. 1984 Apr;151(2):408-20. doi: 10.1016/0014-4827(84)90391-4.
10
Transformation of DNA repair-deficient human diploid fibroblasts with a simian virus 40 plasmid.用猿猴病毒40质粒转化DNA修复缺陷的人类二倍体成纤维细胞。
Exp Cell Res. 1987 Apr;169(2):543-53. doi: 10.1016/0014-4827(87)90214-x.