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大肠杆菌复制起点的DnaA结合位点的突变

Mutations in the DnaA binding sites of the replication origin of Escherichia coli.

作者信息

Holz A, Schaefer C, Gille H, Jueterbock W R, Messer W

机构信息

Max-Planck-Institut für Molekulare Genetik, Berlin, FRG.

出版信息

Mol Gen Genet. 1992 May;233(1-2):81-8. doi: 10.1007/BF00587564.

Abstract

Mutations (base changes) were introduced into the four DnaA binding sites (DnaA boxes) of the Escherichia coli replication origin, oriC. Mutations in a single DnaA box did not impair the ability of these origins to replicate in vivo and in vitro. A combination of mutations in two DnaA boxes, R1 and R4, resulted in slower growth of the oriC plasmid-bearing host cells. DnaA protein interaction with mutant and wild-type DnaA boxes was analyzed by DNase I footprinting. Binding of DnaA protein to a mutated DnaA box R1 was not affected by a mutation in DnaA box R4 and vice versa. Mutations in DnaA boxes R1 and R4 did not modify the ability of the DnaA protein to bind to other DnaA boxes in oriC.

摘要

突变(碱基变化)被引入大肠杆菌复制起点oriC的四个DnaA结合位点(DnaA框)。单个DnaA框中的突变并不损害这些起点在体内和体外的复制能力。两个DnaA框R1和R4中的突变组合导致携带oriC质粒的宿主细胞生长缓慢。通过DNase I足迹法分析了DnaA蛋白与突变型和野生型DnaA框的相互作用。DnaA蛋白与突变的DnaA框R1的结合不受DnaA框R4中突变的影响,反之亦然。DnaA框R1和R4中的突变并未改变DnaA蛋白与oriC中其他DnaA框结合的能力。

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