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SPIRAL2稳定苔藓植物小立碗藓内质微管负端。

SPIRAL2 Stabilises Endoplasmic Microtubule Minus Ends in the Moss Physcomitrella patens.

作者信息

Leong Shu Yao, Yamada Moé, Yanagisawa Naoki, Goshima Gohta

机构信息

Division of Biological Science, Graduate School of Science, Nagoya University.

出版信息

Cell Struct Funct. 2018 Mar 28;43(1):53-60. doi: 10.1247/csf.18001. Epub 2018 Mar 15.

Abstract

Stabilisation of minus ends of microtubules (MTs) is critical for organising MT networks in land plant cells, in which all MTs are nucleated independent of centrosomes. Recently, Arabidopsis SPIRAL2 (SPR2) protein was shown to localise to plus and minus ends of cortical MTs, and increase stability of both ends. Here, we report molecular and functional characterisation of SPR2 of the basal land plant, the moss Physcomitrella patens. In protonemal cells of P. patens, where non-cortical, endoplasmic MT network is organised, we observed SPR2 at minus ends, but not plus ends, of endoplasmic MTs and likely also of phragmoplast MTs. Minus end decoration was reconstituted in vitro using purified SPR2, suggesting that moss SPR2 is a minus end-specific binding protein (-TIP). We generated a loss-of-function mutant of SPR2, in which frameshift-causing deletions/insertions were introduced into all four paralogous SPR2 genes by means of CRISPR/Cas9. Protonemal cells of the mutant showed instability of endoplasmic MT minus ends. These results indicate that moss SPR2 is a MT minus end stabilising factor.Key words: acentrosomal microtubule network, microtubule minus end, P. patens, CAMSAP/Nezha/Patronin.

摘要

微管(MT)负端的稳定对于陆地植物细胞中MT网络的组织至关重要,在陆地植物细胞中,所有MT的成核均独立于中心体。最近,拟南芥SPIRAL2(SPR2)蛋白被证明定位于皮层MT的正端和负端,并增加两端的稳定性。在这里,我们报告了基部陆地植物小立碗藓中SPR2的分子和功能特征。在小立碗藓的原丝体细胞中,非皮层内质网MT网络在此组织,我们在内质网MT的负端而非正端观察到了SPR2,并且在成膜体MT的负端可能也观察到了SPR2。使用纯化的SPR2在体外重建了负端修饰,这表明小立碗藓SPR2是一种负端特异性结合蛋白(-TIP)。我们生成了一个SPR2功能缺失突变体,其中通过CRISPR/Cas9在所有四个同源SPR2基因中引入了导致移码的缺失/插入。突变体的原丝体细胞显示内质网MT负端不稳定。这些结果表明,小立碗藓SPR2是一种MT负端稳定因子。关键词:无中心体微管网络、微管负端、小立碗藓、CAMSAP/Nezha/Patronin 。

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