Suppr超能文献

可渗透人成纤维细胞中的DNA切除修复

DNA excision repair in permeable human fibroblasts.

作者信息

Kaufmann W K, Bodell W J, Cleaver J E

出版信息

Carcinogenesis. 1983;4(2):179-84. doi: 10.1093/carcin/4.2.179.

Abstract

U.v. irradiation of confluent human fibroblasts activated DNA repair, aspects of which were characterized in the cells after they were permeabilized. Incubation of intact cells for 20 min between irradiation and harvesting was necessary to obtain a maximum rate of reparative DNA synthesis. Cells harvested immediately after irradiation before repair was initiated displayed only a small stimulation of DNA synthesis, indicating that permeable cells have a reduced capacity to recognize pyrimidine dimers and activate repair. The distribution of sizes of DNA strands labeled during 10 min of reparative DNA synthesis resembled that of parental DNA. However, during a 60-min incubation of permeable cells at 37 degrees C, parental DNA and DNA labeled by reparative DNA synthesis were both cleaved to smaller sizes. Cleavage also occurred in unirradiated cells, indicating that endogenous nuclease was active during incubation. Repair patches synthesized in permeable cells displayed increased sensitivity to digestion by micrococcal nuclease. However, the change in sensitivity during a chase with unlabeled DNA precursors was small, suggesting that reassembly of nucleosome structure at sites of repair was impaired. To examine whether this deficiency was due to a preponderance of incomplete or unligated repair patches, 3H-labeled (repaired) DNA was purified, then digested with exonuclease III and nuclease S1 to probe for free 3' ends and single-stranded regions. About 85% of the [3H]DNA synthesized during a 10-min pulse resisted digestion, suggesting that a major fraction of the repair patches that were filled were also ligated. U.v. light-activated DNA synthesis in permeable cells, therefore, appears to represent the continuation of reparative gap-filling at sites of excision repair activated within intact cells. Gap-filling and ligation were comparatively efficient processes in permeable cells, whereas activation of reparative DNA synthesis and reassembly of native chromatin structure upon completion of repair were not.

摘要

紫外线照射汇合的人成纤维细胞可激活DNA修复,其中一些方面在细胞透化后进行了表征。在照射和收获之间将完整细胞孵育20分钟对于获得最大的修复性DNA合成速率是必要的。在修复开始前照射后立即收获的细胞仅显示出对DNA合成的轻微刺激,这表明可渗透细胞识别嘧啶二聚体并激活修复的能力降低。在10分钟的修复性DNA合成过程中标记的DNA链大小分布类似于亲本DNA。然而,在37℃下将可渗透细胞孵育60分钟期间,亲本DNA和由修复性DNA合成标记的DNA都被切割成更小的尺寸。未照射的细胞中也发生了切割,这表明内源性核酸酶在孵育期间具有活性。在可渗透细胞中合成的修复补丁对微球菌核酸酶消化的敏感性增加。然而,在用未标记的DNA前体追踪期间敏感性的变化很小,这表明修复位点处核小体结构的重新组装受损。为了检查这种缺陷是否是由于不完全或未连接的修复补丁占优势,纯化了3H标记的(已修复)DNA,然后用核酸外切酶III和核酸酶S1消化以探测游离的3'末端和单链区域。在10分钟脉冲期间合成的约85%的[3H]DNA抵抗消化,这表明填充的修复补丁的大部分也被连接。因此,紫外线激活的可渗透细胞中的DNA合成似乎代表了在完整细胞内激活的切除修复位点处修复性缺口填充的延续。在可渗透细胞中,缺口填充和连接是相对有效的过程,而修复性DNA合成的激活和修复完成后天然染色质结构的重新组装则不然。

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