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大肠杆菌中编码赖氨酰 - tRNA合成酶的两个基因的差异调控:lysU组成型突变可补偿lysS缺失突变。

Differential regulation of two genes encoding lysyl-tRNA synthetases in Escherichia coli: lysU-constitutive mutations compensate for a lysS null mutation.

作者信息

Kawakami K, Ito K, Nakamura Y

机构信息

Department of Tumour Biology, University of Tokyo, Japan.

出版信息

Mol Microbiol. 1992 Jul;6(13):1739-45. doi: 10.1111/j.1365-2958.1992.tb01346.x.

Abstract

Lysyl-tRNA synthetases are synthesized in Escherichia coli from two distinct genes, lysS and lysU, which are regulated differentially. A strain which is null for lysS, the constitutive gene, was created by gene disruption (lysS1) and exhibited cold-sensitive lethality. Hence, lysS is dispensable at high temperatures. This cold sensitivity was suppressed by a multi-copy plasmid carrying lysU, the inducible gene. These data are interpreted as indicating that lysS is functionally replaceable by lysU for cell growth, and that the cold sensitivity of lysS1 is caused by insufficient expression of lysU at low temperatures. To investigate the mechanism of lysU expression, cold-resistant bypass mutations were isolated from lysS1, and named als (for abandonment of lysS). Two als mutations which were linked to lysU contain IS2 insertions upstream of the lysU promoter. They caused a 16-19-fold increase in the lysU-mRNA level. Furthermore, deletion mutations created immediately upstream of the lysU promoter restored growth of lysS1. These results suggest that transcription of lysU is negatively controlled by a cis-element located upstream of the promoter.

摘要

赖氨酰 - tRNA合成酶在大肠杆菌中由两个不同的基因lysS和lysU合成,它们受到不同的调控。通过基因破坏(lysS1)构建了一个对组成型基因lysS无效的菌株,该菌株表现出冷敏感致死性。因此,lysS在高温下是可有可无的。这种冷敏感性被携带诱导型基因lysU的多拷贝质粒所抑制。这些数据被解释为表明lysS在功能上可被lysU替代以支持细胞生长,并且lysS1的冷敏感性是由低温下lysU表达不足引起的。为了研究lysU表达的机制,从lysS1中分离出抗冷旁路突变,并命名为als(代表放弃lysS)。与lysU连锁的两个als突变在lysU启动子上游含有IS2插入。它们使lysU - mRNA水平增加了16 - 19倍。此外,在lysU启动子紧邻上游产生的缺失突变恢复了lysS1的生长。这些结果表明,lysU的转录受到启动子上游一个顺式元件的负调控。

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