Stearns T, Botstein D
Department of Biology, Massachusetts Institute of Technology, Cambridge 02139.
Genetics. 1988 Jun;119(2):249-60. doi: 10.1093/genetics/119.2.249.
Mutations in genes of Saccharomyces cerevisiae that code for proteins that interact with beta-tubulin were sought by screening for unlinked mutations that fail to complement mutations in the single beta-tubulin-encoding gene (TUB2). Among the first three noncomplementing mutations examined, two are linked to TUB2 while one is unlinked. The unlinked mutation was shown to be a conditional-lethal allele of the major alpha-tubulin-encoding gene (TUB1) and represents the first such mutation in that gene. The tub1-1 mutation itself causes a cold-sensitive cell-cycle arrest, and confers supersensitivity to the antimicrotubule drug benomyl. These phenotypes occur in the presence of a wild-type copy of the minor alpha-tubulin-encoding gene, TUB3; the combination of tub1-1 and a tub3 null mutation is inviable in haploids. Through further application of this method, new mutations in TUB2 and TUB3 were isolated as unlinked noncomplementers of tub1-1. The noncomplementation between tub1 and tub2 mutations is gene specific and allele specific, suggesting that the phenotype is due to an interaction at the protein level. We conclude that isolation of unlinked noncomplementing mutations is likely to be a generally useful method for isolating mutations in interacting gene products.
通过筛选与单个β-微管蛋白编码基因(TUB2)中的突变不能互补的非连锁突变,来寻找酿酒酵母中编码与β-微管蛋白相互作用的蛋白质的基因突变。在所检测的前三个非互补突变中,两个与TUB2连锁,而一个不连锁。该不连锁突变被证明是主要α-微管蛋白编码基因(TUB1)的一个条件致死等位基因,并且是该基因中的首个此类突变。tub1-1突变本身会导致冷敏感的细胞周期停滞,并赋予对抗微管药物苯菌灵的超敏感性。这些表型在次要α-微管蛋白编码基因TUB3的野生型拷贝存在的情况下出现;tub1-1与tub3缺失突变的组合在单倍体中是不可存活的。通过进一步应用该方法,分离出了TUB2和TUB3中的新突变,作为tub1-1的非连锁非互补突变。tub1和tub2突变之间的非互补是基因特异性和等位基因特异性的,表明该表型是由于蛋白质水平的相互作用所致。我们得出结论,分离非连锁非互补突变可能是分离相互作用基因产物中突变的一种普遍有用的方法。