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[RAD57基因在酿酒酵母双链DNA缺口修复中的作用]

[Role of the RAD57 gene in the repair of double-stranded DNA gaps in the yeast Saccharomyces cerevisiae].

作者信息

Glazer V M, Glazunov A V

出版信息

Genetika. 1997 Sep;33(9):1221-8.

PMID:9445816
Abstract

The linearized plasmid with complementary (cohesive) ends was shown to restore the circular form in cells of the rad57 mutant with a lower efficiency than in Rad+ cells. This process proved to be cold-sensitive in mutant cells, in contrast to wild-type cells. When mutant cells were shifted from 23 up to 36 degrees C, the repair efficiency increased approximately 1.5 times. In most cases examined, the repair was not accompanied by the doublestrand gap repair within the break site and did not depend on temperature. Homology between chromosomal and plasmid DNA sequences in the break region and the presence of cohesive ends were shown to be essential for the repair of linearized plasmids with a double-strand gap in cells of the rad57 mutant. Degradation of cohesive ends of the linearized plasmid during its repair in rad57 cells is insignificant. Possible mechanisms of linearized plasmid repair in the rad57 mutant are proposed.

摘要

具有互补(粘性)末端的线性化质粒在rad57突变体细胞中恢复为环状形式的效率低于在Rad+细胞中。与野生型细胞相比,这一过程在突变体细胞中被证明是冷敏感的。当突变体细胞从23℃转移到36℃时,修复效率提高了约1.5倍。在大多数检测的情况下,修复过程中断裂位点内不伴有双链缺口修复,且不依赖于温度。已表明断裂区域中染色体与质粒DNA序列之间的同源性以及粘性末端的存在对于rad57突变体细胞中具有双链缺口的线性化质粒的修复至关重要。线性化质粒在rad57细胞修复过程中粘性末端的降解并不显著。本文提出了rad57突变体中线性化质粒修复的可能机制。

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