首页> 美国卫生研究院文献>Journal of Bacteriology >Characterization of dinY a new Escherichia coli DNA repair gene whose products are damage inducible even in a lexA(Def) background.
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Characterization of dinY a new Escherichia coli DNA repair gene whose products are damage inducible even in a lexA(Def) background.

机译:dinY的表征一种新的大肠杆菌DNA修复基因其产物即使在lexA(Def)背景下也可诱导损伤。

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摘要

Bacteriophage Mu dX(Ap lac) was used to isolate a mutation in an Escherichia coli lexA(Def) strain representing a previously undescribed gene (dinY) which does not seem to be under the direct control of LexA. The insertion created a dinY::lacZ fusion in which beta-galactosidase expression required a DNA-damaging treatment (UV irradiation or mitomycin) and activable RecA protein. This strain showed a decreased Weigle reactivation of bacteriophage lambda. However, it was fully inducible for UV mutagenesis. Two-dimensional gel electrophoresis analysis identified two spots absent in the mutant which were both UV inducible only in the presence of activated RecA protein (RecA*). This finding suggests that the dinY::lacZ fusion lies in a gene either that is under the direct control of activated RecA or whose product undergoes RecA*-dependent posttranscriptional/posttranslational modification(s). The dinY gene may also control the expression of some other gene(s) and/or lie in an operon. The fusion was mapped at a position between 41 and 41.5 min on the E. coli chromosome, in the vicinity of the ruv operon.
机译:噬菌体Mu dX(Ap lac)用于分离代表以前未描述的基因(dinY)的大肠杆菌lexA(Def)菌株中的一个突变,该突变似乎不受LexA的直接控制。该插入产生了dinY :: lacZ融合体,其中β-半乳糖苷酶的表达需要DNA损伤处理(紫外线照射或丝裂霉素)和可激活的RecA蛋白。该菌株显示出噬菌体λ的Weigle重新活化降低。但是,它完全可诱导紫外线诱变。二维凝胶电泳分析确定了突变体中不存在的两个斑点,这两个斑点只有在激活的RecA蛋白(RecA *)存在下才可被紫外线诱导。这一发现表明,dinY :: lacZ融合位于一个基因中,该基因处于激活的RecA的直接控制下,或者其产物经历了RecA *依赖性的转录后/翻译后修饰。 dinY基因还可以控制某些其他基因的表达和/或位于操纵子中。将融合体定位在ruv操纵子附近的大肠杆菌染色体上41至41.5分钟之间的位置。

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