STRUCTURAL-ANALYSES OF DNA FRAGMENTS INTEGRATED BY ILLEGITIMATE RECOMBINATION IN SCHIZOSACCHAROMYCES-POMBE

被引:11
|
作者
TATEBAYASHI, K [1 ]
KATO, J [1 ]
IKEDA, H [1 ]
机构
[1] UNIV TOKYO, INST MED SCI, DEPT MOLEC BIOL, TOKYO 108, JAPAN
来源
MOLECULAR AND GENERAL GENETICS | 1994年 / 244卷 / 02期
关键词
ILLEGITIMATE RECOMBINATION; S-POMBE; NONHOMOLOGOUS INTEGRATION; RECOMBINATION JUNCTIONS;
D O I
10.1007/BF00283511
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In order to elucidate the mechanisms of illegitimate recombination in eukaryotes, we have studied the structure of DNA fragments integrated by illegitimate recombination into the genome of fission yeast. Nonhomologous recombination was rarely identified when a long region of homology with the chromosomal leu1(+) gene was present in the introduced leu1::ura4(+) DNA fragment; but a decrease in length of homology leads to an increase in the ratio of nonhomologous to homologous recombination events. The introduced DNA fragments were integrated into different sites in the chromosomes by nonhomologous recombination. The results suggested that there are multiple modes of integration; most events simply involve both ends of the fragments, while in other cases, fragments were integrated in a more complicated manner, probably via circularization or multimerization. To analyze the mechanism of the major type of integration, DNA fragments containing the recombination junctions of three recombinants were amplified by inverted polymerase chain reaction (IPCR) and their nucleotide sequences were determined. There was no obvious homology between introduced DNA and chromosomal DNA at these recombination sites. Furthermore it was found that each terminal region of the introduced DNA was deleted, but that there were no or very small deletions in the target sites of chromosomal DNA. Two models are proposed to explain the mechanism of nonhomologous integration.
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页码:111 / 119
页数:9
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