首页> 美国卫生研究院文献>Cell Regulation >A Highlights from MBoC Selection: Self-organization of stabilized microtubules by both spindle and midzone mechanisms in Xenopus egg cytosol
【2h】

A Highlights from MBoC Selection: Self-organization of stabilized microtubules by both spindle and midzone mechanisms in Xenopus egg cytosol

机译:MBoC选择的一个亮点:非洲爪蟾卵胞质溶胶中梭形和中区机制对稳定化微管的自组织

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Previous study of self-organization of Taxol-stabilized microtubules into asters in Xenopus meiotic extracts revealed motor-dependent organizational mechanisms in the spindle. We revisit this approach using clarified cytosol with glycogen added back to supply energy and reducing equivalents. We added probes for NUMA and Aurora B to reveal microtubule polarity. Taxol and dimethyl sulfoxide promote rapid polymerization of microtubules that slowly self-organize into assemblies with a characteristic morphology consisting of paired lines or open circles of parallel bundles. Minus ends align in NUMA-containing foci on the outside, and plus ends in Aurora B–containing foci on the inside. Assemblies have a well-defined width that depends on initial assembly conditions, but microtubules within them have a broad length distribution. Electron microscopy shows that plus-end foci are coated with electron-dense material and resemble similar foci in monopolar midzones in cells. Functional tests show that two key spindle assembly factors, dynein and kinesin-5, act during assembly as they do in spindles, whereas two key midzone assembly factors, Aurora B and Kif4, act as they do in midzones. These data reveal the richness of self-organizing mechanisms that operate on microtubules after they polymerize in meiotic cytoplasm and provide a biochemically tractable system for investigating plus-end organization in midzones.
机译:在非洲爪蟾减数分裂提取物中紫杉醇稳定的微管自组织为紫苑的先前研究揭示了纺锤体中运动依赖性的组织机制。我们使用澄清的细胞质和糖原重新添加以提供能量和减少当量的方法来重新研究这种方法。我们添加了NUMA和Aurora B探针,以揭示微管极性。紫杉醇和二甲基亚砜促进了微管的快速聚合,这些微管缓慢地自组织成具有由平行线束的成对线或开环组成的特征形态的组件。负端在外侧对齐包含NUMA的焦点,正端在内侧对齐包含Aurora B的焦点。装配体的宽度明确,取决于初始装配条件,但其中的微管长度分布较宽。电子显微镜显示,正向病灶覆盖有电子致密材料,类似于细胞中单极中间区的相似病灶。功能测试表明,两个关键的主轴装配因子dynein和kinesin-5在装配过程中像在主轴中一样起作用,而两个关键的中间区域装配因子Aurora B和Kif4在中间区域中起作用。这些数据揭示了微管在减数分裂细胞质中聚合后对微管起作用的自组织机制的丰富性,并为研究中区的加端组织提供了可生化处理的系统。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号