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大肠杆菌DNA聚合酶III的必需复制亚基ε的水平受热休克蛋白调控。

Levels of epsilon, an essential replication subunit of Escherichia coli DNA polymerase III, are controlled by heat shock proteins.

作者信息

Foster P L, Marinus M G

机构信息

Department of Environmental Health, Boston University School of Public Health, Massachusetts 02118.

出版信息

J Bacteriol. 1992 Dec;174(23):7509-16. doi: 10.1128/jb.174.23.7509-7516.1992.

Abstract

In Escherichia coli, epsilon, the proofreading subunit of DNA polymerase III, is encoded by dnaQ. A random search for mutants that affect the expression of dnaQ revealed that mutations in the genes encoding the heat shock proteins (HSPs) DnaK, DnaJ, and GrpE result in dramatic decreases in the cellular levels of epsilon. dnaQ is arranged in an overlapping divergent transcriptional unit with rnhA, which encodes RNase H1, and mutations in the same HSPs also reduced the apparent levels of RNase H1. The HSPs had only small effects on transcriptional fusions to these genes; thus, it is likely that they operate primarily at the protein level. Since survival and mutagenesis after DNA damage are affected by epsilon and RNase H1, HSPs may have a broad influence on various aspects of DNA replication and repair.

摘要

在大肠杆菌中,DNA聚合酶III的校对亚基ε由dnaQ编码。对影响dnaQ表达的突变体进行随机筛选发现,编码热休克蛋白(HSP)DnaK、DnaJ和GrpE的基因发生突变会导致ε的细胞水平显著下降。dnaQ与编码核糖核酸酶H1的rnhA排列在一个重叠的反向转录单元中,相同热休克蛋白的突变也降低了核糖核酸酶H1的表观水平。热休克蛋白对这些基因的转录融合只有很小的影响;因此,它们可能主要在蛋白质水平发挥作用。由于DNA损伤后的存活和诱变受到ε和核糖核酸酶H1的影响,热休克蛋白可能对DNA复制和修复的各个方面有广泛影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a649/207460/400cbe18f9c9/jbacter00089-0030-a.jpg

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