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自发和诱变诱导的缺失:沙门氏菌测试菌株TA102中的机制研究。

Spontaneous and mutagen-induced deletions: mechanistic studies in Salmonella tester strain TA102.

作者信息

Levin D E, Marnett L J, Ames B N

出版信息

Proc Natl Acad Sci U S A. 1984 Jul;81(14):4457-61. doi: 10.1073/pnas.81.14.4457.

Abstract

Salmonella tester strain TA102 carries the hisG428 ochre mutation on the multicopy plasmid pAQ1. DNA sequence analysis of 45 spontaneous revertants of hisG428 on the chromosome in the presence of pKM101 (strain TA103) indicates that hisG428 revertants fall into three major categories: (i) small, in-frame deletions (3 or 6 base pairs) that remove part or all of the ochre triplet; (ii) base substitution mutations at the ochre site; (iii) extragenic ochre suppressors. Deletion revertants are identified in a simple phenotypic screen by their resistance to the inhibitory histidine analog thiazolealanine, which feedback inhibits the wild-type hisG enzyme but not the enzyme resulting from the deletions. The effect of various genetic backgrounds on the generation of spontaneous deletion revertants was examined. The error-prone repair system encoded in the pKM101 plasmid markedly increased the frequency of total spontaneous reversion events in all genetic backgrounds except recA but did not affect the frequency of spontaneous deletion revertants in any background except polA. The presence of a polA mutation increased the frequency of spontaneous deletion revertants by 2-fold in the absence of pKM101 and by 20-fold with pKM101. The presence of a uvrB mutation or a recA mutation suppressed the generation of spontaneous deletion revertants to approximately 1/2.5. When hisG428 was in multiple copies on pAQ1, the frequency of spontaneous deletion revertants increased by 40-fold, which is the approximate copy number of pAQ1. Mutagenic agents that induce single-strand breaks in DNA (e.g., x-rays, bleomycin, and nalidixic acid) induced deletion revertants in TA102. These agents induced deletion revertants only in hisG428 on pAQ1 and only in the presence of pKM101. Deletion revertants were not induced by frameshift mutagens (i.e., ICR-191 and 9-aminoacridine). These results indicate that different pathways exist for the generation of spontaneous and mutagen-induced deletion revertants of hisG428.

摘要

沙门氏菌测试菌株TA102在多拷贝质粒pAQ1上携带hisG428赭石突变。对存在pKM101(菌株TA103)时染色体上hisG428的45个自发回复突变体进行DNA序列分析表明,hisG428回复突变体分为三大类:(i)小的框内缺失(3或6个碱基对),去除部分或全部赭石三联体;(ii)赭石位点的碱基替代突变;(iii)基因外赭石抑制子。缺失回复突变体通过对抑制性组氨酸类似物噻唑丙氨酸的抗性在简单的表型筛选中得以鉴定,噻唑丙氨酸通过反馈抑制野生型hisG酶,但不抑制缺失产生的酶。研究了各种遗传背景对自发缺失回复突变体产生的影响。pKM101质粒中编码的易错修复系统在除recA外的所有遗传背景中均显著增加了总自发回复事件的频率,但在除polA外的任何背景中均不影响自发缺失回复突变体的频率。在不存在pKM101时,polA突变的存在使自发缺失回复突变体的频率增加2倍,而在存在pKM101时增加20倍。uvrB突变或recA突变的存在将自发缺失回复突变体的产生抑制至约1/2.5。当hisG428在pAQ1上以多拷贝存在时,自发缺失回复突变体的频率增加了40倍,这大约是pAQ1的拷贝数。诱导DNA单链断裂的诱变剂(如X射线、博来霉素和萘啶酸)在TA102中诱导缺失回复突变体。这些诱变剂仅在pAQ1上的hisG428中且仅在存在pKM101时诱导缺失回复突变体。移码诱变剂(即ICR - 191和9 - 氨基吖啶)不会诱导缺失回复突变体。这些结果表明,hisG428的自发和诱变诱导缺失回复突变体的产生存在不同途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94cb/345609/b5508860b0b3/pnas00615-0226-a.jpg

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