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DNA单链断裂的延迟修复不会增加细胞遗传学损伤。

Delayed repair of DNA single-strand breaks does not increase cytogenetic damage.

作者信息

Morgan W F, Djordjevic M C, Jostes R F, Pantelias G E

出版信息

Int J Radiat Biol Relat Stud Phys Chem Med. 1985 Nov;48(5):711-21. doi: 10.1080/09553008514551811.

Abstract

DNA damage and cytogenetic effects of ionizing radiation were investigated in Chinese hamster ovary (CHO) cells and unstimulated human peripheral blood lymphocytes. DNA damage and repair were analysed by alkaline elution under conditions that predominantly measured DNA single-strand breaks (ssb). X-radiation (2.5 Gy) induced ssb in both CHO cells and unstimulated lymphocytes, and the breaks were repaired within 30 and 90 min, respectively. This rapid repair was delayed by the poly(ADP-ribose) polymerase inhibitor, 3-aminobenzamide (3AB). The cytogenetic effects of the 3AB-induced delay in DNA repair were examined by analysing sister chromatid exchange (SCE) frequency in CHO cells and fragmentation of prematurely condensed chromosomes (PCC) in unstimulated human lymphocytes after 2.5 Gy of X-rays. Although 3AB delayed the rejoining of DNA ssb, this delay did not result in increased cytogenetic damage manifested as either SCE or fragmentation of PCC. These results indicate that the rapidly rejoining DNA ssb are not important in the production of chromosome damage.

摘要

在中国仓鼠卵巢(CHO)细胞和未受刺激的人外周血淋巴细胞中研究了电离辐射的DNA损伤和细胞遗传学效应。通过碱性洗脱分析DNA损伤和修复情况,该条件主要检测DNA单链断裂(ssb)。X射线辐射(2.5 Gy)在CHO细胞和未受刺激的淋巴细胞中均诱导产生了ssb,且断裂分别在30分钟和90分钟内得到修复。聚(ADP-核糖)聚合酶抑制剂3-氨基苯甲酰胺(3AB)延迟了这种快速修复。通过分析2.5 Gy X射线照射后CHO细胞中的姐妹染色单体交换(SCE)频率和未受刺激的人淋巴细胞中早熟凝集染色体(PCC)的片段化,研究了3AB诱导的DNA修复延迟的细胞遗传学效应。尽管3AB延迟了DNA ssb的重新连接,但这种延迟并未导致表现为SCE或PCC片段化的细胞遗传学损伤增加。这些结果表明,快速重新连接的DNA ssb在染色体损伤的产生中并不重要。

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