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The effect of nonhomologous DNA sequences on interplasmidic recombination.非同源DNA序列对质粒间重组的影响。
Genetics. 1984 Sep;108(1):39-52. doi: 10.1093/genetics/108.1.39.
2
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本文引用的文献

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Transduction of linked genetic characters of the host by bacteriophage P1.噬菌体P1对宿主连锁遗传性状的转导
Virology. 1955 Jul;1(2):190-206. doi: 10.1016/0042-6822(55)90016-7.
2
recA-independent general genetic recombination of plasmids.质粒的不依赖recA的一般遗传重组
Nature. 1981 Nov 12;294(5837):184-6. doi: 10.1038/294184a0.
3
Effects of nonhomology on bacteriophage lambda recombination.非同源性对噬菌体λ重组的影响。
Genetics. 1983 Jan;103(1):5-22. doi: 10.1093/genetics/103.1.5.
4
Repair tracts in mismatched DNA heteroduplexes.修复错配DNA异源双链体中的修复片段。
Proc Natl Acad Sci U S A. 1976 Nov;73(11):4135-9. doi: 10.1073/pnas.73.11.4135.
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A general model for genetic recombination.遗传重组的通用模型。
Proc Natl Acad Sci U S A. 1975 Jan;72(1):358-61. doi: 10.1073/pnas.72.1.358.
6
pBR322 restriction map derived from the DNA sequence: accurate DNA size markers up to 4361 nucleotide pairs long.源自DNA序列的pBR322限制酶切图谱:长达4361个核苷酸对的精确DNA大小标记。
Nucleic Acids Res. 1978 Aug;5(8):2721-8. doi: 10.1093/nar/5.8.2721.
7
Genetic recombination: strand transfer and mismatch repair.基因重组:链转移与错配修复。
Annu Rev Biochem. 1978;47:847-80. doi: 10.1146/annurev.bi.47.070178.004215.
8
Construction and characterization of amplifiable multicopy DNA cloning vehicles derived from the P15A cryptic miniplasmid.源自P15A隐秘小质粒的可扩增多拷贝DNA克隆载体的构建与表征
J Bacteriol. 1978 Jun;134(3):1141-56. doi: 10.1128/jb.134.3.1141-1156.1978.

非同源DNA序列对质粒间重组的影响。

The effect of nonhomologous DNA sequences on interplasmidic recombination.

作者信息

Laban A, Silberstein Z, Cohen A

出版信息

Genetics. 1984 Sep;108(1):39-52. doi: 10.1093/genetics/108.1.39.

DOI:10.1093/genetics/108.1.39
PMID:6090270
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1202401/
Abstract

The effect of nonhomologous DNA sequences at one or both sides of short genetic intervals on recombination within that interval was investigated, using an interplasmidic recombination system in Escherichia coli K-12. The recombining plasmids were derivatives of pBR322 and pACYC184, which share a 1330-nucleotide sequence that includes the tet gene. The genetic interval was defined by the HindIII and BamHI or BamHI and the SalI restriction endonuclease sites of this gene. The substantial differences between recombination frequencies measured within intervals bracketed or bounded on one side by major nonhomologies suggests that, in this system, strand exchange is polar and is blocked by major nonhomologies. This conclusion is substantiated by results of three-factor crosses and by structural analysis of recombination products. Results of two-factor crosses in recA genetic background and structural analysis of recombination products suggest that strand exchange occurs in the absence of a functional recA gene. "Opening" a bracketed BamHI-SalI genetic interval of the tet gene, at the SalI site, by substituting a major insertion with a short deletion, results in an increase in recombination frequency, within this genetic interval, which is greater than expected on the basis of the ratio of the length of homology on the two sides of the SalI site. This observation suggests that a genetic element that may affect rate of recombination initiation, polarity of strand exchange, template specificity in mismatch repair or more than one of these events may be present on the outer side of the SalI site of the tet gene.

摘要

利用大肠杆菌K - 12中的质粒间重组系统,研究了短遗传间隔一侧或两侧的非同源DNA序列对该间隔内重组的影响。重组质粒是pBR322和pACYC184的衍生物,它们共享一段包含tet基因的1330个核苷酸的序列。遗传间隔由该基因的HindIII和BamHI或BamHI和SalI限制性内切酶位点定义。在一侧由主要非同源序列包围或界定的间隔内测得的重组频率之间的显著差异表明,在该系统中,链交换是极性的,并被主要非同源序列阻断。三因子杂交结果和重组产物的结构分析证实了这一结论。recA遗传背景下的双因子杂交结果和重组产物的结构分析表明,在没有功能性recA基因的情况下也会发生链交换。通过用短缺失替代主要插入片段,在tet基因的SalI位点“打开”括号内的BamHI - SalI遗传间隔,导致该遗传间隔内的重组频率增加,其增加幅度大于基于SalI位点两侧同源长度比所预期的幅度。这一观察结果表明,可能影响重组起始速率、链交换极性、错配修复中的模板特异性或这些事件中的多个事件的遗传元件可能存在于tet基因SalI位点的外侧。