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酿酒酵母DNA修复基因RAD25是RNA聚合酶II转录所必需的。

The Saccharomyces cerevisiae DNA repair gene RAD25 is required for transcription by RNA polymerase II.

作者信息

Qiu H, Park E, Prakash L, Prakash S

机构信息

Department of Biology, University of Rochester, New York 14642.

出版信息

Genes Dev. 1993 Nov;7(11):2161-71. doi: 10.1101/gad.7.11.2161.

Abstract

The RAD25 gene of Saccharomyces cerevisiae is required for excision repair of ultraviolet-damaged DNA and, in addition, is essential for viability. RAD25 shares a high degree of homology with the human ERCC3/XPBC-encoded protein, and the yeast and human proteins resemble one another in containing the conserved ATPase/DNA helicase sequence motifs. To determine the nature of the essential role of RAD25, we have isolated a recessive temperature-sensitive conditional lethal mutation of the gene and have examined its effect on transcription. Upon shift to the nonpermissive temperature, the rad25 temperature-sensitive (ts) mutant stops growth rapidly and shows a large decrease in the synthesis of poly(A)+ RNA. Transcription of a large number of yeast genes, including HIS3, TRP3, STE2, MET19, RAD23, CDC9, and ACT1 is inhibited at the restrictive temperature in the rad25 ts mutant, and the galactose-inducible synthesis of GAL7 and GAL10 mRNAs is also severely affected by the loss of RAD25 activity. These findings implicate a general requirement of RAD25 in RNA polymerase II transcription.

摘要

酿酒酵母的RAD25基因对于紫外线损伤DNA的切除修复是必需的,此外,对于细胞存活也是必不可少的。RAD25与人类ERCC3/XPBC编码的蛋白质具有高度同源性,并且酵母和人类蛋白质在包含保守的ATP酶/DNA解旋酶序列基序方面彼此相似。为了确定RAD25的基本作用的性质,我们分离了该基因的隐性温度敏感型条件致死突变,并研究了其对转录的影响。转移到非允许温度后,rad25温度敏感(ts)突变体迅速停止生长,并显示出多聚腺苷酸(poly(A)+)RNA合成的大幅下降。在rad25 ts突变体中,包括HIS3、TRP3、STE2、MET19、RAD23、CDC9和ACT1在内的大量酵母基因的转录在限制温度下受到抑制,并且RAD25活性的丧失也严重影响了GAL7和GAL10 mRNA的半乳糖诱导合成。这些发现表明RAD25在RNA聚合酶II转录中具有普遍需求。

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