Wordeman L, Steuer E R, Sheetz M P, Mitchison T
Department of Pharmacology, University of California, San Francisco 94143.
J Cell Biol. 1991 Jul;114(2):285-94. doi: 10.1083/jcb.114.2.285.
We have used indirect immunofluorescence in combination with correlative EM to subdivide the mammalian kinetochore into two domains based on the localization of specific antigens. We demonstrate here that the fibrous corona on the distal face of the kinetochore plate contains tubulin (previously shown by Mitchison, T. J., and M. W. Kirschner. 1985. J. Cell Biol. 101:755-765) and the minus end-directed, ATP-dependent microtubule motor protein, dynein; whereas a 50-kD CREST antigen is located internal to these components in the kinetochore. Tubulin and dynein can be extracted from the kinetochore by 150 mM KI, leaving other, as yet uncharacterized, components of the kinetochore corona intact. Microtubules and tubulin subunits will associate with kinetochores in vitro after extraction with 150 mM KI, suggesting that other functionally significant, corona-associated molecules remain unextracted. Our results suggest that the corona region of the kinetochore contains the machinery for chromosome translocation along microtubules.
我们运用间接免疫荧光技术并结合相关电子显微镜技术,根据特定抗原的定位,将哺乳动物的动粒细分为两个结构域。我们在此证明,动粒盘远端表面的纤维冠含有微管蛋白(先前由米奇森和基尔希纳于1985年在《细胞生物学杂志》第101卷第755 - 765页所示)以及负端定向、依赖ATP的微管运动蛋白动力蛋白;而一种50-kD的抗着丝点抗体抗原位于动粒中这些成分的内部。微管蛋白和动力蛋白可通过150 mM KI从动粒中提取出来,而动粒冠的其他尚未明确特征的成分则保持完整。在用150 mM KI提取后,微管和微管蛋白亚基在体外会与动粒结合,这表明其他功能上重要的、与冠相关的分子仍未被提取出来。我们的结果表明,动粒的冠区域包含染色体沿微管进行易位的机制。