Liu C P, Lim J K
Genetics. 1975 Apr;79(4):601-11. doi: 10.1093/genetics/79.4.601.
Recessive lethan mutations in the 3A1 to 3C2 region of the X-chromosome of Drosophila melanogaster were detected in 113 of 33,544 sperm treated by feeding 5 mM methyl methanesulfonate in 1% sucrose for 22 hours. Seven of the 113 lethans were sterile, leaving 106 for analysis by complementation tests. With only one exception, these mutants were found to have lesions restricted to single loci. One of these single-site mutations was in qt, 2 in tko, 18 in zw-1, 12 in zw-8, 6 in zw-4, 3 in zw-10, 3 in zw-13, 21 in zw-2, 7 in zw-3, 5 in zw-6, 6 in zw-12, 1 in zw-7, 12 in zw-5, 5 in zw-11, and 3 in zw-9. One of the lethals, m69, was non-complementary to two adjacent loci, zw-2 and zw-3, possible indicating a deletion encompassing two loci. The results confirm that there are at least 15 recessive lethal loci in the region and are consistent with the hypothesis of LIM and SYNDER (1968 and 1974) that inability of monofunctional alkylating chemicals to induce deletion associated mutations is a characteristic of the compounds.
在用含5 mM甲磺酸甲酯的1%蔗糖溶液处理22小时后的33544个黑腹果蝇精子中,检测到位于X染色体3A1至3C2区域的隐性致死突变113个。113个致死突变中有7个是不育的,剩下106个用于互补测验分析。除了一个例外,这些突变体被发现其损伤仅限于单个位点。这些单一位点突变中,一个位于qt,2个位于tko,18个位于zw-1,12个位于zw-8,6个位于zw-4,3个位于zw-10,3个位于zw-13,21个位于zw-2,7个位于zw-3,5个位于zw-6,6个位于zw-12,1个位于zw-7,12个位于zw-5,5个位于zw-11,3个位于zw-9。其中一个致死突变体m69与两个相邻位点zw-2和zw-3不互补,这可能表明存在一个包含两个位点的缺失。结果证实该区域至少有15个隐性致死位点,并且与LIM和SYNDER(1968年和1974年)的假说一致,即单功能烷基化化学物质不能诱导缺失相关突变是这些化合物的一个特征。