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当归素光敏化哺乳动物细胞中RNA合成的损伤及其恢复。一种DNA损伤与修复的探针。

Impairment of RNA synthesis and its recovery in angelicin photosensitized mammalian cells. A probe for DNA damage and repair.

作者信息

Nocentini S

出版信息

Biochim Biophys Acta. 1978 Nov 21;521(1):160-8. doi: 10.1016/0005-2787(78)90259-9.

Abstract

The template activity of DNA for ribosomal RNA transcription has been investigated in monkey kidney CV-1 cells after angelicin photosensitization in order to monitor the induction of lesions in the DNA and their possible subsequent disappearance, i.e. repair. Separate confluent cultures were submitted to a single angelicin treatment at different time intervals before incubation with [3H]uridine. The labeled RNA prepared from whole cells was analysed by polyacrylamide-agarose gel electrophoresis. The results indicate that: Angelicin monoadditions on DNA constitute transcription-terminating lesions which depress overall RNA synthesis, give rise to shortened RNA chains and modify the expression of transcriptional linked genes. CV-1 cells are able to repair, at least partially, the induced transcription-terminating lesions and progressively recover RNA synthesis with a reversion of the initially observed modifications. The repair seems to be independent of semiconservative DNA synthesis since fluorodeoxyuridine does not affect the recovery of RNA transcription. The present work also confirms the arrangement of rRNA genes in tandem behind a common operator in the order 18--28 S as previously determined in the same cells by a radiological mapping technique and reinforces the potential applicability of transcription analysis to the study of repair processes operating on physically or chemically induced damage in DNA.

摘要

为监测DNA损伤的诱导及其可能随后的消失,即修复,在用补骨脂素进行光敏处理后,对猴肾CV - 1细胞中核糖体RNA转录的DNA模板活性进行了研究。在与[³H]尿苷孵育之前,将不同汇合的培养物在不同时间间隔进行单次补骨脂素处理。从全细胞制备的标记RNA通过聚丙烯酰胺 - 琼脂糖凝胶电泳进行分析。结果表明:DNA上的补骨脂素单加成构成转录终止损伤,其抑制整体RNA合成,产生缩短的RNA链并改变转录连锁基因的表达。CV - 1细胞能够至少部分修复诱导的转录终止损伤,并随着最初观察到的修饰的逆转而逐渐恢复RNA合成。修复似乎独立于半保留DNA合成,因为氟脱氧尿苷不影响RNA转录的恢复。本研究还证实了rRNA基因在同一细胞中先前通过放射图谱技术确定的顺序为18 - 28 S的共同操纵子后面串联排列,并加强了转录分析在研究DNA物理或化学诱导损伤的修复过程中的潜在适用性。

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