De Stasio E, Lephoto C, Azuma L, Holst C, Stanislaus D, Uttam J
Department of Biology, Lawrence University, Appleton, Wisconsin 54911, USA.
Genetics. 1997 Oct;147(2):597-608. doi: 10.1093/genetics/147.2.597.
Phenotypic reversion of the rubber-band, muscle-defective phenotype conferred by unc-93(e1500) was used to determine the utility of N-ethyl-N-nitrosourea (ENU) as a mutagen for genetic research in Caenorhabditis elegans. In this system, ENU produces revertants at a frequency of 3 x 10(-4), equivalent to that of the commonly used mutagen, EMS. The gene identity of 154 ENU-induced revertants shows that the distribution of alleles between three possible suppressor genes differs from induced by EMS. A higher percentage of revertants are alleles of unc-93 and many fewer are alleles of sup-9 and sup-10. Three revertants complement the three known suppressor genes; they may therefore identify a new gene product(s) involved in this system of excitation-contraction coupling in C. elegans. Molecular characterization of putative unc-93 null alleles reveals that the base changes induced by ENU are quite different from those induced by EMS; specifically we see an increased frequency of A/T-->G/C transitions. The frequency of ENU-induced intragenic deletions is found to be 13%. We suggest that ENU, at concentrations below 5 mM, will be a superior mutagen for studies of protein function in C. elegans.
利用unc-93(e1500)赋予的橡皮筋状、肌肉缺陷型表型的表型回复来确定N-乙基-N-亚硝基脲(ENU)作为秀丽隐杆线虫遗传研究诱变剂的效用。在这个系统中,ENU产生回复突变体的频率为3×10^(-4),与常用诱变剂EMS相当。154个ENU诱导的回复突变体的基因鉴定表明,三个可能的抑制基因之间的等位基因分布与EMS诱导的不同。较高比例的回复突变体是unc-93的等位基因,而sup-9和sup-10的等位基因则少得多。三个回复突变体与三个已知的抑制基因互补;因此,它们可能鉴定出参与秀丽隐杆线虫兴奋-收缩偶联系统的一种新的基因产物。假定的unc-93无效等位基因的分子特征表明,ENU诱导的碱基变化与EMS诱导的有很大不同;具体来说,我们观察到A/T→G/C转换的频率增加。发现ENU诱导的基因内缺失频率为13%。我们认为,浓度低于5 mM的ENU将是秀丽隐杆线虫蛋白质功能研究的一种更优诱变剂。