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定量分析recA、recB、recC、recF、recJ、recN、lexA、radA、radB、uvrD和umuC基因在大肠杆菌修复X射线诱导的DNA双链断裂中的作用。

Quantitation of the involvement of the recA, recB, recC, recF, recJ, recN, lexA, radA, radB, uvrD, and umuC genes in the repair of X-ray-induced DNA double-strand breaks in Escherichia coli.

作者信息

Sargentini N J, Smith K C

出版信息

Radiat Res. 1986 Jul;107(1):58-72.

PMID:3526390
Abstract

Isogenic Escherichia coli strains carrying single DNA-repair mutations were compared for their capacity for (i) the repair of X-ray-induced DNA double-strand breaks (DSB) as measured using neutral sucrose gradients; (ii) medium-dependent resistance, i.e., a recA-dependent X-ray survival phenomenon that correlates closely with the capacity for repairing DSB; and (iii) the growth medium-dependent, recA-dependent repair of X-ray-induced DNA single-strand breaks (SSB) as measured using alkaline sucrose gradients (about 80% of these SSB are actually parts of DSB). These three capacities were measured to quantitate more accurately the involvement of the various genes in the repair of DSB over a wide dose range. The mutations tested were grouped into five classes according to their effect on the repair of X-ray-induced DSB: (I) the recA, recB, recC, and lexA mutants were completely deficient; (II) the radB and recN mutants were about 90% deficient; (III) the recF and recJ mutants were about 70% deficient; (IV) the radA and uvrD mutants were about 30% deficient; and (V) the umuC mutant resembled the wild-type strains in its capacity for the repair of DSB.

摘要

对携带单个DNA修复突变的同基因大肠杆菌菌株进行了以下方面能力的比较:(i)使用中性蔗糖梯度测量X射线诱导的DNA双链断裂(DSB)的修复能力;(ii)培养基依赖性抗性,即一种与recA相关的X射线存活现象,与DSB修复能力密切相关;(iii)使用碱性蔗糖梯度测量X射线诱导的DNA单链断裂(SSB)的生长培养基依赖性、recA依赖性修复(这些SSB中约80%实际上是DSB的一部分)。测量这三种能力是为了在较宽剂量范围内更准确地定量各种基因在DSB修复中的参与情况。根据对X射线诱导的DSB修复的影响,测试的突变分为五类:(I)recA、recB、recC和lexA突变体完全缺陷;(II)radB和recN突变体约90%缺陷;(III)recF和recJ突变体约70%缺陷;(IV)radA和uvrD突变体约30%缺陷;(V)umuC突变体在DSB修复能力方面与野生型菌株相似。

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