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缺乏HU蛋白的大肠杆菌突变体中的DNA复制

DNA replication in Escherichia coli mutants that lack protein HU.

作者信息

Ogawa T, Wada M, Kano Y, Imamoto F, Okazaki T

机构信息

Department of Molecular Biology, School of Science, Nagoya University, Japan.

出版信息

J Bacteriol. 1989 Oct;171(10):5672-9. doi: 10.1128/jb.171.10.5672-5679.1989.

Abstract

DNA replication in Escherichia coli cells lacking protein HU was studied. HU has been suggested to be involved in the initiation of replication from in vitro studies. The isolated HU mutants, however, are viable under normal growth conditions (M. Wada, Y. Kano, T. Ogawa, T. Okazaki, and F. Imamoto, J. Mol. Biol. 204:581-591, 1988). Chromosomal replication in the mutants appeared to be normal with respect to bidirectional replication from oriC and to its dependence on dnaA and some other dna gene products. No significant defect was observed in DNA synthesis in vitro with a crude enzyme fraction prepared from the mutant cells. These results, along with the earlier in vitro studies, suggest that other histonelike protein(s) may substitute for HU in the initiation of replication in the mutant cells. Minichromosomes were more unstable in the mutants. In the absence of either the mioC promoter, from which transcription enters oriC, or the DnaA box (DnaA protein-binding site) just upstream of the mioC promoter, the minichromosomes were especially unstable in the HU mutant and were integrated into the chromosomal oriC region under conditions selective for the plasmid-harboring cells.

摘要

对缺乏蛋白质HU的大肠杆菌细胞中的DNA复制进行了研究。体外研究表明HU参与复制起始。然而,分离得到的HU突变体在正常生长条件下是存活的(M. Wada、Y. Kano、T. Ogawa、T. Okazaki和F. Imamoto,《分子生物学杂志》204:581 - 591,1988)。突变体中的染色体复制在从oriC双向复制以及对dnaA和其他一些dna基因产物的依赖性方面似乎是正常的。用从突变体细胞制备的粗酶组分进行体外DNA合成时,未观察到明显缺陷。这些结果与早期的体外研究一起表明,其他类组蛋白可能在突变体细胞的复制起始中替代HU。微型染色体在突变体中更不稳定。在缺乏转录进入oriC的mioC启动子或mioC启动子上游的DnaA框(DnaA蛋白结合位点)的情况下,微型染色体在HU突变体中特别不稳定,并在对携带质粒的细胞有选择性的条件下整合到染色体oriC区域。

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