Cizeau J, Decoville M, Leng M, Locker D
CBM CNRS, Orléans, France.
Mutat Res. 1994 Nov 1;311(1):31-8. doi: 10.1016/0027-5107(94)90070-1.
This paper describes the analysis of cisplatin induced mutations at the white (w) and vermilion (v) loci located on the X chromosome of Drosophila melanogaster. Twenty-eight w and eight v mutants have been found in a male genetic context and 42 w mutants in a female genetic context. In these latter experiments, genetic analysis showed the presence of multi-locus deficiencies in 18 out of 42 w mutants. Eighteen w and three v intragenic mutations were analyzed at the molecular level. Seventeen w and three v mutants carry deletions within the gene, ranging in size from 4 to 109 base pairs. Sequence analysis of the mutants indicates that most of them were produced by non-homologous recombinational events occurring between short (2-5 bp) sequence repeats on both sides of the deletion, one repeat being retained at the new junction. These results differ largely from those obtained in prokaryotic and other eukaryotic cells.
本文描述了对顺铂诱导位于黑腹果蝇X染色体上的白眼(w)和朱红眼(v)位点突变的分析。在雄性遗传背景下发现了28个w突变体和8个v突变体,在雌性遗传背景下发现了42个w突变体。在这些后续实验中,遗传分析表明42个w突变体中有18个存在多位点缺失。对18个w基因内突变和3个v基因内突变进行了分子水平分析。17个w突变体和3个v突变体在基因内携带缺失,缺失大小从4到109个碱基对不等。对这些突变体的序列分析表明,它们大多数是由缺失两侧短(2 - 5个碱基对)序列重复之间发生的非同源重组事件产生的,其中一个重复保留在新的连接处。这些结果与在原核细胞和其他真核细胞中获得的结果有很大不同。