Patterson B, Spudich J A
Department of Biochemistry, Beckman Center, Stanford University, California 94305, USA.
Genetics. 1995 Jun;140(2):505-15. doi: 10.1093/genetics/140.2.505.
We developed a positive selection for myosin heavy chain mutants in Dictyostelium. This selection is based on the fact that brief exposure to azide causes wild-type cells to release from the substrate, whereas myosin null cells remain adherent. This procedure assays myosin function on a time scale of minutes and has therefore allowed us to select rapid-onset cold-sensitive mutants after random chemical mutagenesis of Dictyostelium cells. We developed a rapid technique for determining which mutations lie in sequences of the myosin gene that encode the head (motor) domain and localized 27 of 34 mutants to this domain. We recovered the appropriate sequences from five of the mutants and demonstrated that they retain their cold-sensitive properties when expressed from extrachromosomal plasmids.
我们开发了一种针对盘基网柄菌中肌球蛋白重链突变体的正向选择方法。这种选择基于这样一个事实:短暂暴露于叠氮化物会使野生型细胞从底物上脱离,而肌球蛋白缺失细胞仍保持附着。该程序在几分钟的时间尺度上检测肌球蛋白功能,因此使我们能够在对盘基网柄菌细胞进行随机化学诱变后选择快速起效的冷敏感突变体。我们开发了一种快速技术,用于确定哪些突变位于编码头部(运动)结构域的肌球蛋白基因序列中,并将34个突变体中的27个定位到该结构域。我们从其中5个突变体中回收了相应序列,并证明当从染色体外质粒表达时,它们保留了冷敏感特性。