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一种与噬菌体T4的v基因产物相关的嘧啶二聚体-DNA糖基化酶活性。

A pyrimidine dimer-DNA glycosylase activity associated with the v gene product of bacterophage T4.

作者信息

Radany E H, Friedberg E C

出版信息

Nature. 1980 Jul 10;286(5769):182-5. doi: 10.1038/286182a0.

Abstract

Mutations in the v gene of bacteriophage T4 are associated with a marked increase in sensitivity to killing by UV radiation at 254 nm, but not to a variety of other forms of base damage to DNA. Early studies from this laboratory provided evidence for a role of the v gene in the excision of pyrimidine dimers (PD) from DNA. Specifically, it was shown that extracts of T4v+-infected Escherichia coli catalyse the formation of single-strand breaks (nicks) and/or alkali-labile sites in UIV-irradiated duplex DNA. Comparable hydrolysis of phosphodiester bonds is not observed with extracts of E. coli infected with the mutant T4v1 (ref. 5). The product of the v gene has been extensively purified in a number of laboratories; however, convincing evidence of purification to physical homogeneity has not yet been presented.

摘要

噬菌体T4的v基因发生突变与对254nm紫外线辐射杀伤的敏感性显著增加有关,但与DNA的多种其他形式的碱基损伤无关。本实验室早期的研究为v基因在从DNA中切除嘧啶二聚体(PD)中的作用提供了证据。具体而言,研究表明,受T4v +感染的大肠杆菌提取物可催化紫外线照射的双链DNA中单链断裂(切口)和/或碱不稳定位点的形成。用突变体T4v1感染的大肠杆菌提取物未观察到磷酸二酯键的类似水解(参考文献5)。v基因的产物已在多个实验室中得到广泛纯化;然而,尚未有令人信服的证据表明已纯化至物理均一性。

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