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在减数分裂提取物中微管的组装需要糖原。

Microtubule assembly in meiotic extract requires glycogen.

机构信息

Department of Systems Biology, Harvard Medical School, Boston, MA 02115, USA.

出版信息

Mol Biol Cell. 2011 Sep;22(17):3139-51. doi: 10.1091/mbc.E11-02-0158. Epub 2011 Jul 7.

Abstract

The assembly of microtubules during mitosis requires many identified components, such as γ-tubulin ring complex (γ-TuRC), components of the Ran pathway (e.g., TPX2, HuRP, and Rae1), and XMAP215/chTOG. However, it is far from clear how these factors function together or whether more factors exist. In this study, we used biochemistry to attempt to identify active microtubule nucleation protein complexes from Xenopus meiotic egg extracts. Unexpectedly, we found both microtubule assembly and bipolar spindle assembly required glycogen, which acted both as a crowding agent and as metabolic source glucose. By also reconstituting microtubule assembly in clarified extracts, we showed microtubule assembly does not require ribosomes, mitochondria, or membranes. Our clarified extracts will provide a powerful tool for activity-based biochemical fractionations for microtubule assembly.

摘要

在有丝分裂过程中微管的组装需要许多已鉴定的成分,如γ-微管蛋白环复合物(γ-TuRC)、Ran 途径的成分(例如,TPX2、HuRP 和 Rae1)和 XMAP215/chTOG。然而,这些因素如何协同作用,或者是否存在更多的因素,还远不清楚。在这项研究中,我们使用生物化学方法从非洲爪蟾减数分裂卵提取物中尝试鉴定有活性的微管核蛋白复合物。出乎意料的是,我们发现微管组装和双极纺锤体组装都需要糖原,糖原既作为拥挤剂又作为代谢葡萄糖的来源。通过在澄清提取物中重新组装微管,我们表明微管组装不需要核糖体、线粒体或膜。我们的澄清提取物将为基于活性的微管组装生化分级分离提供一个强大的工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/659b/3164461/43c35e626926/3139fig1.jpg

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