Batzer M A, Tedeschi B, Fossett N G, Tucker A, Kilroy G, Arbour P, Lee W R
Department of Zoology and Physiology, Louisiana State University, Baton Rouge 70803.
Mutat Res. 1988 May;199(1):255-68. doi: 10.1016/0027-5107(88)90253-9.
Mutations induced in Drosophila spermatozoa at the alcohol dehydrogenase Adh locus by 1-ethyl-1-nitrosourea (ENU) were compared to X-ray-induced mutations using genetic tests for complementation, southern blotting, western blotting and northern blotting. 8 of 10 ENU-induced mutations complemented all known adjacent loci and were presumed to be intragenic. In contrast, 8 of 30 X-ray-induced mutations were intragenic. Southern blot analysis showed that 2 of 7 intragenic mutations induced by X-rays were altered at the Adh locus, whereas all 8 intragenic ENU mutants appeared normal. Western blot analysis showed 4 of 7 intragenic mutants induced by X-rays produced a detectable polypeptide; 1 of the 4 had normal molecular weight and charge. In contrast, 7 of the 8 intragenic mutants induced by ENU produced a polypeptide of normal molecular weight and charge. One ENU and two X-ray-induced mutants, which had normal southern blots and no detectable polypeptide, produced normal molecular weight mRNA by northern blots. The interpretation of these results is that in spermatozoa X-rays induce primarily deletions that either produce deficiencies of the Adh locus or nonsense mutations within the locus, whereas ENU induces primarily missense mutations. This forward mutation assay based on loss of enzymatic activity efficiently recovered a broad spectrum of mutations ranging from missense to intragenic deletions and multi-locus deficiencies. Only 3 of these 40 mutations produced a polypeptide detectable as an electrophoretic variant.
利用互补基因检测、Southern印迹法、Western印迹法和Northern印迹法,将1-乙基-1-亚硝基脲(ENU)诱导果蝇精子中乙醇脱氢酶Adh基因座发生的突变与X射线诱导的突变进行了比较。10个ENU诱导的突变中有8个与所有已知相邻基因座互补,推测为基因内突变。相比之下,30个X射线诱导的突变中有8个是基因内突变。Southern印迹分析表明,X射线诱导的7个基因内突变中有2个在Adh基因座发生了改变,而所有8个ENU诱导的基因内突变体看起来都是正常的。Western印迹分析表明,X射线诱导的7个基因内突变体中有4个产生了可检测到的多肽;其中4个中有1个具有正常的分子量和电荷。相比之下,ENU诱导的8个基因内突变体中有7个产生了分子量和电荷正常的多肽。1个ENU诱导的突变体和2个X射线诱导的突变体,其Southern印迹正常且未检测到多肽,但通过Northern印迹产生了分子量正常的mRNA。这些结果的解释是,在精子中,X射线主要诱导缺失,这些缺失要么导致Adh基因座的缺陷,要么导致该基因座内的无义突变,而ENU主要诱导错义突变。这种基于酶活性丧失的正向突变检测方法有效地恢复了从错义突变到基因内缺失和多位点缺陷的广泛突变谱。这40个突变中只有3个产生了可作为电泳变体检测到的多肽。