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首页> 外文期刊>Frontiers in Cell and Developmental Biology >Anaphase Chromosomes in Crane-Fly Spermatocytes Treated With Taxol (Paclitaxel) Accelerate When Their Kinetochore Microtubules Are Cut: Evidence for Spindle Matrix Involvement With Spindle Forces
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Anaphase Chromosomes in Crane-Fly Spermatocytes Treated With Taxol (Paclitaxel) Accelerate When Their Kinetochore Microtubules Are Cut: Evidence for Spindle Matrix Involvement With Spindle Forces

机译:用紫杉醇(紫杉醇)治疗的起重机 - 飞染细胞中的后染色体在切割运动中切割时加速:主轴矩阵的证据参与主轴力

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Various experiments have indicated that anaphase chromosomes continue to move after their kinetochore microtubules are severed. The chromosomes move poleward at an accelerated rate after the microtubules are cut but they slow down 1-3 minutes later and move poleward at near the original speed. There are two published interpretations of chromosome movements with severed kinetochore microtubules. One interpretation is that dynein relocates to the severed microtubule ends and propels them poleward by pushing against non-kinetochore microtubules. The other interpretation is that components of a putative ‘spindle matrix’ normally push kinetochore microtubules poleward and continue to do so after the microtubules are severed from the pole. In this study we distinguish between these interpretations by treating cells with taxol. Taxol eliminates microtubule dynamics, alters spindle microtubule arrangements, and inhibits dynein motor activity in vivo. If the dynein interpretation is correct, taxol should interfere with chromosome movements after kinetochore microtubules are severed because it alters the arrangements of spindle microtubules and because it blocks dynein activity. If the ‘spindle matrix’ interpretation is correct, on the other hand, taxol should not interfere with the accelerated movements. Our results support the spindle matrix interpretation: anaphase chromosomes in taxol-treated crane-fly spermatocytes accelerated after their kinetochore microtubules were severed.
机译:各种实验表明,在切断的运动芯管微管后,外延染色体继续移动。切割微管后,染色体以加速速率向极端移动,但它们后1-3分钟后速度减慢,并在近原始速度下移动。用切断的Kinetochore微管有两种发布的染色体运动解释。一种解释是Dynein迁移到切断的微管末端,并通过推动非运动棘爪微管来推动它们。另一个解释是推定的“主轴矩阵”的部件通常推动KINETOCHORE微管杆极端,并且在从杆中切断微管后,继续这样做。在这项研究中,我们通过用紫杉醇治疗细胞来区分这些解释。紫杉醇消除了微管动态,改变了主轴微管布置,并抑制体内Dynein Motor活性。如果Dynein解释是正确的,紫杉醇应该干扰Kinetochore Microtubules切断后的染色体运动,因为它改变了主轴微管的布置,因为它阻断了Dynein活性。另一方面,如果“主轴矩阵”解释是正确的,则紫杉醇不应干扰加速运动。我们的结果支持主轴矩阵解释:紫杉醇治疗的起重机的染色体染色体在切断其Kinetochore微管后加速。

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