Moore J D, Endow S A
Department of Microbiology, Duke University Medical Center, Durham, NC 27710, USA.
Bioessays. 1996 Mar;18(3):207-19. doi: 10.1002/bies.950180308.
The cellular processes of transport, division and, possibly, early development all involve microtubule-based motors. Recent work shows that, unexpectedly, many of these cellular functions are carried out by different types of kinesin and kinesin-related motor proteins. The kinesin proteins are a large and rapidly growing family of microtubule-motor proteins that share a 340-amino-acid motor domain. Phylogenetic analysis of the conserved motor domains groups the kinesin proteins into a number of subfamilies, the members of which exhibit a common molecular organization and related functions. The kinesin proteins that belong to different subfamilies differ in their rates and polarity of movement along microtubules, and probably in the particles/organelles that they transport. The kinesins arose early in eukaryotic evolution and gene duplication has allowed functional specialization to occur, resulting in a surprisingly large number of different classes of these proteins adapted for intracellular transport of vesicles and organelles, and for assembly and force generation in the meiotic and mitotic spindles.
运输、分裂以及可能的早期发育等细胞过程均涉及基于微管的马达蛋白。最近的研究表明,出人意料的是,许多此类细胞功能是由不同类型的驱动蛋白和与驱动蛋白相关的马达蛋白执行的。驱动蛋白是一个庞大且数量迅速增长的微管马达蛋白家族,它们共享一个由340个氨基酸组成的马达结构域。对保守马达结构域的系统发育分析将驱动蛋白分为若干亚家族,其中的成员展现出共同的分子结构和相关功能。属于不同亚家族的驱动蛋白在沿微管移动的速度和极性方面存在差异,并且在它们所运输的颗粒/细胞器方面可能也有所不同。驱动蛋白在真核生物进化早期就已出现,基因复制使得功能特化得以发生,从而产生了数量惊人的不同类别的此类蛋白,这些蛋白适用于囊泡和细胞器的细胞内运输,以及减数分裂和有丝分裂纺锤体的组装和力的产生。