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EB1 通过招募果蝇细胞中的 Sentin 促进微管动力学。

EB1 promotes microtubule dynamics by recruiting Sentin in Drosophila cells.

机构信息

Division of Biological Science, Graduate School of Science, Nagoya University, Nagoya 464-8601, Japan.

出版信息

J Cell Biol. 2011 Jun 13;193(6):973-83. doi: 10.1083/jcb.201101108. Epub 2011 Jun 6.

Abstract

Highly conserved EB1 family proteins bind to the growing ends of microtubules, recruit multiple cargo proteins, and are critical for making dynamic microtubules in vivo. However, it is unclear how these master regulators of microtubule plus ends promote microtubule dynamics. In this paper, we identify a novel EB1 cargo protein, Sentin. Sentin depletion in Drosophila melanogaster S2 cells, similar to EB1 depletion, resulted in an increase in microtubule pausing and led to the formation of shorter spindles, without displacing EB1 from growing microtubules. We demonstrate that Sentin's association with EB1 was critical for its plus end localization and function. Furthermore, the EB1 phenotype was rescued by expressing an EBN-Sentin fusion protein in which the C-terminal cargo-binding region of EB1 is replaced with Sentin. Knockdown of Sentin attenuated plus end accumulation of Msps (mini spindles), the orthologue of XMAP215 microtubule polymerase. These results indicate that EB1 promotes dynamic microtubule behavior by recruiting the cargo protein Sentin and possibly also a microtubule polymerase to the microtubule tip.

摘要

高度保守的 EB1 家族蛋白与微管的生长末端结合,招募多个货物蛋白,对于体内形成动态微管至关重要。然而,这些微管正极端的主要调节因子如何促进微管动力学尚不清楚。在本文中,我们鉴定了一种新的 EB1 货物蛋白 Sentin。在果蝇 S2 细胞中敲低 Sentin,与敲低 EB1 相似,导致微管停顿增加,并导致较短的纺锤体形成,而不会将 EB1 从生长中的微管上置换。我们证明了 Sentin 与 EB1 的结合对于其正极端定位和功能至关重要。此外,在表达将 EB1 的 C 末端货物结合区域替换为 Sentin 的 EBN-Sentin 融合蛋白的情况下,EB1 表型得到挽救。Sentin 的敲低减弱了 Msps(微型纺锤体),即微管聚合酶 XMAP215 的同源物,在正极端的积累。这些结果表明,EB1 通过招募货物蛋白 Sentin 并可能还有微管聚合酶到微管尖端来促进动态微管行为。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f1d/3115803/3648512bc809/JCB_201101108_RGB_Fig1.jpg

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