Paweletz N, Lang U
Institute of Cell and Tumor Biology, German Cancer Research Center, Heidelberg, Federal Republic of Germany.
Eur J Cell Biol. 1988 Dec;47(2):334-45.
When cells in mitosis are treated with nocodazole, a microtubule-disrupting drug, it can be shown in comparison to untreated cells that microtubules are responsible for the polarized formation of indentations, folds, tubes, and crypts of the nuclear envelope in prophase nuclei. No translocation of chromosomes within the nucleus takes place. Microtubules are not necessary for chromosome condensation, nuclear envelope breakdown, the formation of trilaminar kinetochores, and the orientation of sister-kinetochores within one chromosome in relation to each other. The orientation of kinetochores in relation to the mitotic poles, however, is mediated by microtubules. The data shown here support the working hypothesis about chromosome translocation in prophase nuclei which was presented in an earlier paper.
当用诺考达唑(一种破坏微管的药物)处理处于有丝分裂期的细胞时,与未处理的细胞相比,可以发现微管负责前期细胞核中核膜凹陷、褶皱、管状结构和隐窝的极化形成。细胞核内染色体不会发生易位。微管对于染色体凝聚、核膜破裂、三层动粒的形成以及一条染色体中姐妹动粒彼此之间的定向并非必需。然而,动粒相对于有丝分裂极的定向是由微管介导的。此处所示数据支持了早期一篇论文中提出的关于前期细胞核中染色体易位的工作假说。