Maddox P S, Bloom K S, Salmon E D
Department of Biology, CB3280, University of North Carolina, Chapel Hill, North Carolina 27599-3280, USA.
Nat Cell Biol. 2000 Jan;2(1):36-41. doi: 10.1038/71357.
Microtubule assembly in Saccharomyces cerevisiae is initiated from sites within spindle pole bodies (SPBs) in the nuclear envelope. Microtubule plus ends are thought to be organized distal to the SPBs, while minus ends are proximal. Several hypotheses for the function of microtubule motor proteins in force generation and regulation of microtubule assembly propose that assembly and disassembly occur at minus ends as well as at plus ends. Here we analyse microtubule assembly relative to the SPBs in haploid yeast cells expressing green fluorescent protein fused to alpha-tubulin, a microtubule subunit. Throughout the cell cycle, analysis of fluorescent speckle marks on cytoplasmic astral microtubules reveals that there is no detectable assembly or disassembly at minus ends. After laser-photobleaching, metaphase spindles recover about 63% of the bleached fluorescence, with a half-life of about 1 minute. After anaphase onset, photobleached marks in the interpolar spindle are persistent and do not move relative to the SPBs. In late anaphase, the elongated spindles disassemble at the microtubule plus ends. These results show for astral and anaphase interpolar spindle microtubules, and possibly for metaphase spindle microtubules, that microtubule assembly and disassembly occur at plus, and not minus, ends.
酿酒酵母中的微管组装起始于核膜内纺锤极体(SPB)内的位点。微管的正端被认为位于SPB的远端,而负端则位于近端。关于微管运动蛋白在力的产生和微管组装调节中的作用,有几种假说提出组装和解聚在负端以及正端都会发生。在这里,我们分析了在表达与微管亚基α-微管蛋白融合的绿色荧光蛋白的单倍体酵母细胞中,微管相对于SPB的组装情况。在整个细胞周期中,对细胞质星状微管上的荧光斑点标记进行分析发现,负端没有可检测到的组装或解聚。激光漂白后,中期纺锤体恢复了约63%的漂白荧光,半衰期约为1分钟。后期开始后,极间纺锤体中的漂白标记持续存在,并且相对于SPB不移动。在后期末期,伸长的纺锤体在微管正端解聚。这些结果表明,对于星状和后期极间纺锤体微管,可能对于中期纺锤体微管也是如此,微管的组装和解聚发生在正端,而不是负端。