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范可尼贫血中丝裂霉素C交联修复缺陷以及汇合的正常人细胞和着色性干皮病细胞中的修复缺失。

Defective repair of mitomycin C crosslinks in Fanconi's anemia and loss in confluent normal human and xeroderma pigmentosum cells.

作者信息

Fujiwara Y

出版信息

Biochim Biophys Acta. 1982 Dec 31;699(3):217-25. doi: 10.1016/0167-4781(82)90110-5.

Abstract

Crosslink repair of mitomycin C-induced interstrand crosslinks was studied in exponentially growing and confluent normal human, transformed W138CT-1, Fanconi's anemia (FA) and xeroderma pigmentosum (XP) group-A fibroblasts by the assay methods of alkaline sucrose centrifugation, hydroxyapatite column chromatography and S1-nuclease digestion. These three methods demonstrated unequivocally that crosslinking occurred at a rate of 0.13 crosslinks/10(8) Da per microgram per ml mitomycin C (less than or equal to 10 micrograms/ml) and the first half-excision of crosslinks followed the rapid first-order kinetics of 2-3 h half-life in exponentially-growing normal, WI38CT-1 and XP group-A cells. However, the first half-excision was completely defective in three out of the four FA strains tested and severely retarded in an FA strain. These results strongly support our previous observations in different strains of normal human, FA and XP group-A cells. An important new addition is that confluent, otherwise proficient, normal and XP cells almost completely lost the ability of the first, rapid half-excision of mitomycin C crosslinks in their DNA. This probably suggests that the enzyme or regulatory factor responsible for the half-excision, which differs from that for nucleotide excision repair, present constitutively in confluent cells, may be induced or activated only in the cycling cells. However, its relation to a defective FA factor is not clear at present.

摘要

通过碱性蔗糖密度梯度离心、羟基磷灰石柱层析和S1核酸酶消化等检测方法,对指数生长期和汇合状态的正常人成纤维细胞、转化的W138CT - 1细胞、范可尼贫血(FA)细胞和着色性干皮病(XP)A组细胞中丝裂霉素C诱导的链间交联修复进行了研究。这三种方法明确表明,交联以每毫升每微克丝裂霉素C(≤10微克/毫升)0.13个交联/10⁸道尔顿的速率发生,在指数生长期的正常细胞、WI38CT - 1细胞和XP A组细胞中,交联的首次半切除遵循半衰期为2 - 3小时的快速一级动力学。然而,在所检测的4个FA细胞株中有3个的首次半切除完全缺陷,另一个FA细胞株中则严重延迟。这些结果有力地支持了我们之前在不同株正常人、FA和XP A组细胞中的观察结果。一个重要的新发现是,汇合状态下原本修复能力正常的正常细胞和XP细胞几乎完全丧失了对其DNA中丝裂霉素C交联进行首次快速半切除的能力。这可能表明,负责半切除的酶或调节因子不同于核苷酸切除修复相关的酶或调节因子,在汇合细胞中组成性存在,可能仅在增殖细胞中被诱导或激活。然而,目前其与缺陷的FA因子的关系尚不清楚。

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