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肺炎链球菌互补性DpnI和DpnII限制系统的遗传基础:一种细胞间盒式机制。

Genetic basis of the complementary DpnI and DpnII restriction systems of S. pneumoniae: an intercellular cassette mechanism.

作者信息

Lacks S A, Mannarelli B M, Springhorn S S, Greenberg B

出版信息

Cell. 1986 Sep 26;46(7):993-1000. doi: 10.1016/0092-8674(86)90698-7.

Abstract

Cells of S. pneumoniae contain either DpnI, a restriction endonuclease that cleaves only the methylated DNA sequence 5'-GmeATC-3', or DpnII, which cleaves the same sequence when not methylated. A chromosomal DNA segment containing DpnII genes was cloned in S. pneumoniae. Nucleotide sequencing of this segment revealed genes encoding the methylase and endonuclease and a third protein of unknown function. When the plasmid was introduced into DpnI cells, recombination during chromosomal facilitation of its establishment substituted genes encoding the DpnI endonuclease and another protein in place of the DpnII genes. DNA hybridization and sequencing showed that the DpnI and DpnII segments share homology on either side but not between themselves or with other regions of the chromosome. Thus, the complementary restriction systems are found on nonhomologous and mutually exclusive cassettes that can be inserted into a particular point in the chromosome of S. pneumoniae on the basis of neighboring homology.

摘要

肺炎链球菌的细胞要么含有DpnI,一种仅切割甲基化DNA序列5'-GmeATC-3'的限制性内切酶,要么含有DpnII,当该序列未甲基化时它会切割相同序列。一段包含DpnII基因的染色体DNA片段在肺炎链球菌中被克隆。该片段的核苷酸测序揭示了编码甲基化酶、内切酶以及第三种功能未知蛋白质的基因。当将该质粒导入含有DpnI的细胞时,在其建立过程中的染色体促进作用期间的重组用编码DpnI内切酶和另一种蛋白质的基因取代了DpnII基因。DNA杂交和测序表明,DpnI和DpnII片段在两侧具有同源性,但它们自身之间或与染色体的其他区域没有同源性。因此,互补的限制系统存在于非同源且相互排斥的盒式结构上,这些盒式结构可基于相邻同源性插入到肺炎链球菌染色体的特定位置。

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