Department of Molecular Genetics, The Ohio State University, Columbus, OH 43210, USA.
J Cell Biol. 2010 Aug 9;190(3):317-30. doi: 10.1083/jcb.201002105. Epub 2010 Aug 2.
A cold-sensitive gamma-tubulin allele of Aspergillus nidulans, mipAD159, causes defects in mitotic and cell cycle regulation at restrictive temperatures that are apparently independent of microtubule nucleation defects. Time-lapse microscopy of fluorescently tagged mitotic regulatory proteins reveals that cyclin B, cyclin-dependent kinase 1, and the Ancdc14 phosphatase fail to accumulate in a subset of nuclei at restrictive temperatures. These nuclei are permanently removed from the cell cycle, whereas other nuclei, in the same multinucleate cell, cycle normally, accumulating and degrading these proteins. After each mitosis, additional daughter nuclei fail to accumulate these proteins, resulting in an increase in noncycling nuclei over time and consequent inhibition of growth. Extensive analyses reveal that these noncycling nuclei result from a nuclear autonomous, microtubule-independent failure of inactivation of the anaphase-promoting complex/cyclosome. Thus, gamma-tubulin functions to regulate this key mitotic and cell cycle regulatory complex.
阿舒假囊霉冷敏感γ-微管蛋白等位基因 mipAD159 在限制温度下导致有丝分裂和细胞周期调控缺陷,这些缺陷显然与微管成核缺陷无关。对荧光标记的有丝分裂调节蛋白进行延时显微镜观察显示,细胞周期蛋白 B、细胞周期蛋白依赖性激酶 1 和 Ancdc14 磷酸酶在限制温度下无法在一部分核中积累。这些核永久地从细胞周期中去除,而同一多核细胞中的其他核则正常循环,积累和降解这些蛋白质。在每次有丝分裂后,额外的子核无法积累这些蛋白质,导致非循环核随时间增加,并导致生长受到抑制。广泛的分析表明,这些非循环核是由于有丝分裂促进复合物/细胞周期蛋白环的核自主、微管独立失活的失败导致的。因此,γ-微管蛋白的功能是调节这个关键的有丝分裂和细胞周期调节复合物。