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一种黑腹果蝇品系中的诱变因子:通过突变、回复突变率和雄性重组来鉴定。

A mutator factor in a strain of Drosophila melanogaster: identified by use of mutation, reversion rates and male recombination.

作者信息

Scobie N N, Schaffer H E

出版信息

Genetics. 1982 Jul-Aug;101(3-4):417-29. doi: 10.1093/genetics/101.3-4.417.

Abstract

A set of 1,000 "mutation accumulation" lines Drosophila melanogaster, which originated from two different wild-type, lethal-bearing second chromosomes (Yamaguchi and Mukai 1974; Mukai and Cockerham 1977), was examined for evidence of a mutator factor by using the occurrence of recessive visible mutations and male recombination to identify its presence. The 1,000 lines were screened at approximately generation 240 for the presence of recessive visible mutation at twelve loci, by outcrossing to a balanced multiply marked second chromosome stock (Muller's "12ple" Bowling Green). Twenty-three lines were found to carry a visible mutation at one of the vg locus. mutations found in three lines, two at the dp locus and one at the vg locus, demonstrated instability as revertants to the wild type and were recovered and verified in these three cases. The three revertant lines, and three lines showing no reversion, were tested for their ability to induce male recombination. Male recombination was observed in the three lines in which revertants were recovered. Male and female sterility assays indicated conclusively that these "hybrid dysgenic" characteristics could not be used to identify lines potentially carrying mutator factors, whereas the consistent ability of the lines to induce high rates of reversion and male recombination was successful in determining that the "mutation accumulation lines" do possess mutator factors.

摘要

一组1000个黑腹果蝇的“突变积累”品系,源自两条不同的野生型、携带致死基因的第二染色体(山口和向井,1974年;向井和科克伦,1977年),通过利用隐性可见突变的出现和雄性重组来确定其存在,以检测是否存在突变因子。在大约第240代时,通过与一个平衡的多重标记第二染色体品系(穆勒的“12ple”,鲍灵格林)杂交,对这1000个品系进行筛选,以检测12个位点上隐性可见突变的存在。发现有23个品系在vg位点之一携带可见突变。在三个品系中发现的突变,两个在dp位点,一个在vg位点,表现出向野生型回复突变的不稳定性,并在这三个案例中得到了恢复和验证。对三个回复品系和三个未表现出回复的品系进行了诱导雄性重组能力的测试。在恢复了回复突变体的三个品系中观察到了雄性重组。雄性和雌性不育测定最终表明,这些“杂种劣生”特征不能用于识别可能携带突变因子的品系,而这些品系一致诱导高频率回复突变和雄性重组的能力成功地确定了“突变积累品系”确实具有突变因子。

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