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用8-甲氧基补骨脂素和近紫外线或X射线处理后,正常和范科尼贫血成纤维细胞中的DNA半保留合成

DNA semi-conservative synthesis in normal and Fanconi anemia fibroblasts following treatment with 8-methoxypsoralen and near ultraviolet light or with X-rays.

作者信息

Moustacchi E, Diatloff-Zito C

出版信息

Hum Genet. 1985;70(3):236-42. doi: 10.1007/BF00273448.

Abstract

The effect of treatment with 8-methoxypsoralen (8-MOP) plus near-UV radiation (UVA) or with X-rays on the rate of DNA semi-conservative synthesis of fibroblasts from 10 Fanconi anemia (FA), two heterozygous, and three normal cell lines was studied. Following treatments with either X-rays or low doses of 8-MOP plus UVA leading to a majority of monoadducts over cross-links per genome, the FA and heterozygous cell lines were indistinguishable from normals: the transient inhibition of semi-conservative DNA synthesis was followed by the recovery of a normal rate of synthesis. In contrast treatment with higher (but not saturating) doses of 8-MOP plus UVA allowed us to distinguish two classes among the FA cell lines. One class demonstrated a pattern of recovery similar to that of heterozygous and normal cell lines. This indicates that in such cell lines, the predominant lesion in this condition, the cross-links, do not arrest DNA synthesis and are likely to be normally repaired. Another class of FA cell lines did not show a recovery of a normal rate of DNA synthesis even after prolonged post-treatment incubation and although the proportion of cells in S phase was similar to that of the strains of the first category. This indicates that in such cell lines the repair of cross-links is inhibited at some step which is not necessarily the incision one.

摘要

研究了用8-甲氧基补骨脂素(8-MOP)加近紫外线辐射(UVA)或X射线处理对来自10个范可尼贫血(FA)、2个杂合子和3个正常细胞系的成纤维细胞DNA半保留合成速率的影响。在用X射线或低剂量的8-MOP加UVA处理后,每个基因组中大多数为单加合物而非交联物,FA和杂合子细胞系与正常细胞系没有区别:半保留DNA合成的短暂抑制之后是合成速率恢复正常。相比之下,用较高(但不饱和)剂量的8-MOP加UVA处理使我们能够在FA细胞系中区分出两类。一类表现出与杂合子和正常细胞系相似的恢复模式。这表明在这类细胞系中,这种情况下的主要损伤——交联物,不会阻止DNA合成,并且可能被正常修复。另一类FA细胞系即使在处理后长时间孵育后也没有显示出DNA合成速率恢复正常,尽管S期细胞的比例与第一类细胞系相似。这表明在这类细胞系中,交联物的修复在某个步骤受到抑制,而不一定是切口步骤。

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