Buster Daniel W, Zhang Dong, Sharp David J
Department of Physiology and Biophysics, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Mol Biol Cell. 2007 Aug;18(8):3094-104. doi: 10.1091/mbc.e06-11-0994. Epub 2007 Jun 6.
The poleward flux of tubulin subunits through spindle microtubules is a striking and conserved phenomenon whose function and molecular components remain poorly understood. To screen for novel components of the flux machinery, we utilized RNA interference to deplete regulators of microtubule dynamics, individually and in various combinations, from S2 cells and examined the resulting impact on flux rate. This led to the identification of two previously unknown flux inhibitors, KLP59C and KLP67A, and a flux promoter, Mini-spindles. Furthermore, we find that flux rate is regulated by functional antagonism among microtubule stabilizers and destabilizers specifically at plus ends. Finally, by examining mitosis on spindles in which flux has been up- or down-regulated or restored after the codepletion of antagonistic flux regulators, we show that flux is an integral contributor to anaphase A but is not responsible for chromosome congression, interkinetochore tension, or the establishment of normal spindle length during prometaphase/metaphase.
微管蛋白亚基通过纺锤体微管向极区的通量是一种显著且保守的现象,但其功能和分子组成仍知之甚少。为了筛选通量机制的新组分,我们利用RNA干扰技术,从S2细胞中单独或多种组合地耗尽微管动力学的调节因子,并检查其对通量率的影响。这导致鉴定出两种先前未知的通量抑制剂KLP59C和KLP67A,以及一种通量促进因子Mini-spindles。此外,我们发现通量率由微管稳定剂和去稳定剂之间特别是在正端的功能拮抗作用调节。最后,通过检查在拮抗通量调节因子共耗尽后通量已上调、下调或恢复的纺锤体上的有丝分裂,我们表明通量是后期A的一个重要贡献因素,但对染色体排列、动粒间张力或前中期/中期正常纺锤体长度的建立没有作用。