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分析莲座状巨核的核孔 NUP107-160 亚基复合物揭示了明显的结构可塑性和功能冗余。

Analysis of the Lotus japonicus nuclear pore NUP107-160 subcomplex reveals pronounced structural plasticity and functional redundancy.

机构信息

Faculty of Biology, Genetics, University of Munich Martinsried, Germany.

出版信息

Front Plant Sci. 2014 Jan 22;4:552. doi: 10.3389/fpls.2013.00552. eCollection 2013.

DOI:10.3389/fpls.2013.00552
PMID:24478780
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3897872/
Abstract

Mutations in the Lotus japonicus nucleoporin genes, NUP85, NUP133, and NENA (SEH1), lead to defects in plant-microbe symbiotic signaling. The homologous proteins in yeast and vertebrates are part of the conserved NUP84/NUP107-160 subcomplex, which is an essential component of the nuclear pore scaffold and has a pivotal role in nuclear pore complex (NPC) assembly. Loss and down-regulation of NUP84/NUP107-160 members has previously been correlated with a variety of growth and molecular defects, however, in L. japonicus only surprisingly specific phenotypes have been reported. We investigated whether Lotus nup85, nup133, and nena mutants exhibit general defects in NPC composition and distribution. Whole mount immunolocalization confirmed a typical nucleoporin-like localization for NUP133, which was unchanged in the nup85-1 mutant. Severe NPC clustering and aberrations in the nuclear envelope have been reported for Saccharomyces cerevisiae nup85 and nup133 mutants. However, upon transmission electron microscopy analysis of L. japonicus nup85, nup133 and nena, we detected only a slight reduction in the average distances between neighboring NPCs in nup133. Using quantitative immunodetection on protein-blots we observed that loss of individual nucleoporins affected the protein levels of other NUP107-160 complex members. Unlike the single mutants, nup85/nup133 double mutants exhibited severe temperature dependent growth and developmental defects, suggesting that the loss of more than one NUP107-160 member affects basal functions of the NPC.

摘要

在豌豆中,核孔蛋白基因 NUP85、NUP133 和 NENA(SEH1)的突变会导致植物-微生物共生信号转导缺陷。酵母和脊椎动物中的同源蛋白是保守的 NUP84/NUP107-160 亚复合物的一部分,该复合物是核孔支架的重要组成部分,在核孔复合物(NPC)组装中起着关键作用。以前,NUP84/NUP107-160 成员的缺失和下调与多种生长和分子缺陷有关,但在豌豆中,仅报道了非常特异的表型。我们研究了 Lotus nup85、nup133 和 nena 突变体是否表现出 NPC 组成和分布的普遍缺陷。全挂载免疫定位证实了 NUP133 的典型核孔蛋白样定位,在 nup85-1 突变体中未改变。在酿酒酵母 nup85 和 nup133 突变体中,已经报道了 NPC 聚类和核膜异常。然而,在对豌豆 nup85、nup133 和 nena 进行透射电子显微镜分析时,我们仅检测到 nup133 中相邻 NPC 之间的平均距离略有减少。通过对蛋白印迹进行定量免疫检测,我们观察到单个核孔蛋白的缺失会影响其他 NUP107-160 复合物成员的蛋白水平。与单突变体不同,nup85/nup133 双突变体表现出严重的依赖温度的生长和发育缺陷,这表明失去一个以上的 NUP107-160 成员会影响 NPC 的基本功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da00/3897872/5af32d995c88/fpls-04-00552-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da00/3897872/eef7630cfac1/fpls-04-00552-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da00/3897872/5876ccfbcb7c/fpls-04-00552-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da00/3897872/1a869978f5ed/fpls-04-00552-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da00/3897872/5af32d995c88/fpls-04-00552-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da00/3897872/eef7630cfac1/fpls-04-00552-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da00/3897872/5876ccfbcb7c/fpls-04-00552-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da00/3897872/1a869978f5ed/fpls-04-00552-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da00/3897872/5af32d995c88/fpls-04-00552-g0004.jpg

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