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pBR322中聚[d(GT)-d(CA)]的RecA非依赖性重组

RecA independent recombination of poly[d(GT)-d(CA)] in pBR322.

作者信息

Murphy K E, Stringer J R

出版信息

Nucleic Acids Res. 1986 Sep 25;14(18):7325-40. doi: 10.1093/nar/14.18.7325.

Abstract

Short sequence tracts composed of alternating guanosine and thymidine nucleotide residues poly[d(GT)-d(CA)] carried in a derivative of pBR322 were recombinogenic in a recA host. Recombination brought about by poly[d(GT)-d(CA)] tracts displayed two interesting properties: (i) the reaction was quasi-sequence-specific in that while recombination usually occurred between two poly[d(GT)-d(CA)] tracts, recombination also occurred between sequences bordering the dinucleotide repeats. (ii) recombination was enhanced when two poly[d(GT)-d(CA)] tracts were clustered within 250 base pairs of each other, but not when the repeats were separated by 3 kilobase pairs. The mechanism by which poly[d(GT)-d(CA)] stimulated recombination remains to be determined, but the behavior of these sequences is consistent with the idea that general recombination in E. coli may involve formation of Z-DNA.

摘要

携带于pBR322衍生物中的由鸟苷和胸苷核苷酸残基交替组成的短序列片段聚[d(GT)-d(CA)]在recA宿主中具有重组活性。由聚[d(GT)-d(CA)]片段引发的重组表现出两个有趣的特性:(i) 该反应具有准序列特异性,即虽然重组通常发生在两个聚[d(GT)-d(CA)]片段之间,但也会发生在二核苷酸重复序列相邻的序列之间。(ii) 当两个聚[d(GT)-d(CA)]片段彼此聚集在250个碱基对范围内时,重组增强,但当重复序列被3千碱基对隔开时则不然。聚[d(GT)-d(CA)]刺激重组的机制尚待确定,但这些序列的行为与大肠杆菌中的一般重组可能涉及Z-DNA形成的观点一致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a33/311754/8ee12ddaa410/nar00287-0191-a.jpg

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