• 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

来自正常人及着色性干皮病染色质的两种DNA内切酶活性,对补骨脂素加紫外线处理的DNA具有活性。

Two DNA endonuclease activities from normal human and xeroderma pigmentosum chromatin active on psoralen plus ultraviolet light treated DNA.

作者信息

Lambert M W, Fenkart D, Clarke M

机构信息

Department of Pathology, UMDNJ-New Jersey Medical School, Newark 07103.

出版信息

Mutat Res. 1988 Jan;193(1):65-73. doi: 10.1016/0167-8817(88)90008-9.

DOI:10.1016/0167-8817(88)90008-9
PMID:3336371
Abstract

DNA endonuclease activities from the chromatin of normal human and xeroderma pigmentosum, complementation group A (XPA), lymphoblastoid cells were examined on DNA treated with 8-methoxypsoralen (8-MOP) or 4,5',8-trimethylpsoralen (TMP) plus long wavelength ultraviolet (UVA) light, which produce monoadducts and DNA interstrand cross-links, and angelicin plus UVA light, which produces mainly monoadducts. 9 chromatin-associated DNA endonuclease activities were isolated from normal and XPA cells and assayed for activity on PM2 bacteriophage DNA that had been treated with 8-MOP or TMP in the dark and then exposed to UVA light. Unbound psoralen was removed by dialysis and a second dose of UVA light was given. Cross-linking of DNA molecules was confirmed by alkaline gel electrophoresis. In both normal and XPA cells, two DNA endonuclease activities were found which were active on 8-MOP and TMP plus UVA light treated DNA. One of these endonuclease activities, pI 4.6, is also active on intercalated DNA and a second one, pI 7.6, is also active on UVC (254 nm) light irradiated DNA. The major activity against angelicin plus UVA light treated DNA in both normal and XPA cells was found in the fraction, pI 7.6. The levels of activity of both of these fractions on all 3 psoralen-damaged DNAs were similar between normal and XPA cells. These results indicate that in both normal and XPA cells there are at least two different DNA endonucleases which act on both 8-MOP and TMP plus UVA light treated DNA.

摘要

对正常人及着色性干皮病A组(XPA)淋巴母细胞染色质中的DNA内切酶活性进行了检测,检测对象为经8-甲氧基补骨脂素(8-MOP)或4,5',8-三甲基补骨脂素(TMP)加长波紫外线(UVA)照射处理的DNA,这两种处理会产生单加合物和DNA链间交联,以及经当归素加UVA照射处理的DNA,这种处理主要产生单加合物。从正常细胞和XPA细胞中分离出9种与染色质相关的DNA内切酶活性,并检测其对在黑暗中用8-MOP或TMP处理后再暴露于UVA光的PM2噬菌体DNA的活性。通过透析去除未结合的补骨脂素,并给予第二剂UVA光。通过碱性凝胶电泳确认DNA分子的交联。在正常细胞和XPA细胞中,均发现两种对8-MOP和TMP加UVA光处理的DNA有活性的DNA内切酶活性。其中一种内切酶活性,pI为4.6,对插入的DNA也有活性,另一种,pI为7.6,对紫外线C(254nm)照射的DNA也有活性。在正常细胞和XPA细胞中,针对当归素加UVA光处理的DNA的主要活性存在于pI为7.6的组分中。正常细胞和XPA细胞中这两种组分对所有3种补骨脂素损伤的DNA的活性水平相似。这些结果表明,在正常细胞和XPA细胞中,至少有两种不同的DNA内切酶作用于8-MOP和TMP加UVA光处理的DNA。

相似文献

1
Two DNA endonuclease activities from normal human and xeroderma pigmentosum chromatin active on psoralen plus ultraviolet light treated DNA.来自正常人及着色性干皮病染色质的两种DNA内切酶活性,对补骨脂素加紫外线处理的DNA具有活性。
Mutat Res. 1988 Jan;193(1):65-73. doi: 10.1016/0167-8817(88)90008-9.
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
Defective DNA endonuclease activities in Fanconi's anemia cells, complementation groups A and B.范可尼贫血症细胞中A组和B组互补群的DNA内切酶活性缺陷
Mutat Res. 1992 Jan;273(1):57-71. doi: 10.1016/0921-8777(92)90050-d.
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
Correction of the ultraviolet light induced DNA-repair defect in xeroderma pigmentosum cells by electroporation of a normal human endonuclease.通过电穿孔导入正常人内切核酸酶纠正着色性干皮病细胞中紫外线诱导的DNA修复缺陷
Mutat Res. 1990 Jul;244(3):257-63. doi: 10.1016/0165-7992(90)90138-a.
6
Electroporation of normal human DNA endonucleases into xeroderma pigmentosum cells corrects their DNA repair defect.将正常人DNA内切酶电穿孔导入着色性干皮病细胞可纠正其DNA修复缺陷。
Carcinogenesis. 1990 Mar;11(3):499-503. doi: 10.1093/carcin/11.3.499.
7
Induction and repair of psoralen cross-links in DNA of normal human and xeroderma pigmentosum fibroblasts.补骨脂素在正常人及着色性干皮病成纤维细胞DNA中交联的诱导与修复
Mutat Res. 1982 Mar;93(1):221-34. doi: 10.1016/0027-5107(82)90137-3.
8
A processive versus a distributive mechanism of action correlates with differences in ability of normal and xeroderma pigmentosum group A endonucleases to incise damaged nucleosomal DNA.持续性作用机制与分布性作用机制的差异,与正常内切酶和着色性干皮病A组内切酶切割受损核小体DNA能力的差异相关。
Carcinogenesis. 1997 Feb;18(2):279-86. doi: 10.1093/carcin/18.2.279.
9
Deficient DNA binding of an apurinic/apyrimidinic DNA endonuclease activity from xeroderma pigmentosum cells.
Cell Biol Int Rep. 1988 Mar;12(3):231-7. doi: 10.1016/0309-1651(88)90100-2.
10
Xeroderma pigmentosum complementation group A protein acts as a processivity factor.着色性干皮病A互补组蛋白作为一种持续合成因子发挥作用。
Biochem Biophys Res Commun. 2000 May 19;271(3):782-7. doi: 10.1006/bbrc.2000.2714.

引用本文的文献

1
Defining the roles of nucleotide excision repair and recombination in the repair of DNA interstrand cross-links in mammalian cells.确定核苷酸切除修复和重组在哺乳动物细胞DNA链间交联修复中的作用。
Mol Cell Biol. 2000 Nov;20(21):7980-90. doi: 10.1128/MCB.20.21.7980-7990.2000.
2
8-Methoxypsoralen induced mutations are highly targeted at crosslinkable sites of photoaddition on the non-transcribed strand of a mammalian chromosomal gene.8-甲氧基补骨脂素诱导的突变高度靶向于哺乳动物染色体基因非转录链上光加成的可交联位点。
EMBO J. 1993 Feb;12(2):397-402. doi: 10.1002/j.1460-2075.1993.tb05671.x.
3
A damage-recognition protein which binds to DNA containing interstrand cross-links is absent or defective in Fanconi anemia, complementation group A, cells.
在范可尼贫血互补组A细胞中,一种与含有链间交联的DNA结合的损伤识别蛋白缺失或存在缺陷。
Nucleic Acids Res. 1993 Sep 11;21(18):4187-92. doi: 10.1093/nar/21.18.4187.
4
Genomic damage and its repair in young and aging brain.年轻及衰老大脑中的基因组损伤及其修复
Mol Neurobiol. 1993 Spring;7(1):23-48. doi: 10.1007/BF02780607.