McDonald H B, Goldstein L S
Department of Cellular and Developmental Biology, Harvard University, Cambridge, Massachusetts 02138.
Cell. 1990 Jun 15;61(6):991-1000. doi: 10.1016/0092-8674(90)90064-l.
We identified and sequenced a cDNA clone encoding a kinesin-like protein from Drosophila. The predicted product of this cDNA has a carboxy-terminal domain that is substantially similar to the motor domain of kinesin heavy chain. The amino-terminal domain is unlike that found in previously identified kinesins or kinesin-like proteins. Analyses of this new sequence suggest that the maximal motor unit in the kinesin superfamily may be as little as 350 amino acids, and that the existence of both kinesin and kinesin-like molecules must be an evolutionarily ancient feature of eukaryotes. We also tested some of the biochemical properties of the protein encoded by this cDNA and found them to be similar to those of kinesin. Finally, the clone we isolated appears to correspond to the non-claret disjunctional (ncd) gene, which when mutant causes defects in meiotic and early embryonic mitotic chromosome segregation, and whose recently determined sequence predicts a kinesin-like domain.
我们从果蝇中鉴定并测序了一个编码类驱动蛋白的cDNA克隆。该cDNA的预测产物具有一个羧基末端结构域,它与驱动蛋白重链的运动结构域基本相似。氨基末端结构域与先前鉴定的驱动蛋白或类驱动蛋白中的结构域不同。对这个新序列的分析表明,驱动蛋白超家族中的最大运动单元可能只有350个氨基酸,并且驱动蛋白和类驱动蛋白分子的存在必定是真核生物进化史上古老的特征。我们还测试了该cDNA编码的蛋白质的一些生化特性,发现它们与驱动蛋白的生化特性相似。最后,我们分离出的克隆似乎对应于非红葡萄酒不分离(ncd)基因,该基因发生突变时会导致减数分裂和早期胚胎有丝分裂染色体分离缺陷,并且其最近确定的序列预测有一个类驱动蛋白结构域。