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锥虫核孔结构的详细表征揭示了驱动mRNA输出的保守不对称功能中心。

Detailed characterisation of the trypanosome nuclear pore architecture reveals conserved asymmetrical functional hubs that drive mRNA export.

作者信息

Gabiatti Bernardo Papini, Krenzer Johanna, Braune Silke, Krüger Timothy, Zoltner Martin, Kramer Susanne

机构信息

Biocenter, University of Würzburg, Würzburg, Germany.

Department of Parasitology, Faculty of Science, Charles University in Prague, Biocev, Vestec, Prague, Czech Republic.

出版信息

PLoS Biol. 2025 Feb 3;23(2):e3003024. doi: 10.1371/journal.pbio.3003024. eCollection 2025 Feb.

Abstract

Nuclear export of mRNAs requires loading the mRNP to the transporter Mex67/Mtr2 in the nucleoplasm, controlled access to the pore by the basket-localised TREX-2 complex and mRNA release at the cytoplasmic site by the DEAD-box RNA helicase Dbp5. Asymmetric localisation of nucleoporins (NUPs) and transport components as well as the ATP dependency of Dbp5 ensure unidirectionality of transport. Trypanosomes possess homologues of the mRNA transporter Mex67/Mtr2, but not of TREX-2 or Dbp5. Instead, nuclear export is likely fuelled by the GTP/GDP gradient created by the Ran GTPase. However, it remains unclear, how directionality is achieved since the current model of the trypanosomatid pore is mostly symmetric. We have revisited the architecture of the trypanosome nuclear pore complex using a novel combination of expansion microscopy, proximity labelling and streptavidin imaging. We could confidently assign the NUP76 complex, a known Mex67 interaction platform, to the cytoplasmic site of the pore and the NUP64/NUP98/NUP75 complex to the nuclear site. Having defined markers for both sites of the pore, we set out to map all 75 trypanosome proteins with known nuclear pore localisation to a subregion of the pore using mass spectrometry data from proximity labelling. This approach defined several further proteins with a specific localisation to the nuclear site of the pore, including proteins with predicted structural homology to TREX-2 components. We mapped the components of the Ran-based mRNA export system to the nuclear site (RanBPL), the cytoplasmic site (RanGAP, RanBP1) or both (Ran, MEX67). Lastly, we demonstrate, by deploying an auxin degron system, that NUP76 holds an essential role in mRNA export consistent with a possible functional orthology to NUP82/88. Altogether, the combination of proximity labelling with expansion microscopy revealed an asymmetric architecture of the trypanosome nuclear pore supporting inherent roles for directed transport. Our approach delivered novel nuclear pore associated components inclusive positional information, which can now be interrogated for functional roles to explore trypanosome-specific adaptions of the nuclear basket, export control, and mRNP remodelling.

摘要

mRNA的核输出需要将mRNP装载到核质中的转运蛋白Mex67/Mtr2上,由位于篮状结构的TREX-2复合物控制进入核孔,并通过DEAD-box RNA解旋酶Dbp5在细胞质位点释放mRNA。核孔蛋白(NUPs)和转运成分的不对称定位以及Dbp5对ATP的依赖性确保了转运的单向性。锥虫具有mRNA转运蛋白Mex67/Mtr2的同源物,但不具有TREX-2或Dbp5的同源物。相反,核输出可能由Ran GTP酶产生的GTP/GDP梯度驱动。然而,由于目前锥虫核孔模型大多是对称的,方向性是如何实现的仍不清楚。我们使用超分辨显微镜、邻近标记和链霉亲和素成像的新组合重新研究了锥虫核孔复合体的结构。我们可以确定已知的Mex67相互作用平台NUP76复合物位于核孔的细胞质位点,而NUP64/NUP98/NUP75复合物位于核位点。在确定了核孔两个位点的标记后,我们利用邻近标记的质谱数据,将所有75种已知核孔定位的锥虫蛋白映射到核孔的一个子区域。这种方法确定了几种进一步定位于核孔核位点的蛋白,包括与TREX-2成分具有预测结构同源性的蛋白。我们将基于Ran的mRNA输出系统的成分映射到核位点(RanBPL)、细胞质位点(RanGAP、RanBP1)或两者(Ran、MEX67)。最后,我们通过部署生长素降解系统证明,NUP76在mRNA输出中起着至关重要的作用,这与NUP82/88可能的功能同源性一致。总之,邻近标记与超分辨显微镜的结合揭示了锥虫核孔的不对称结构,支持了定向转运的固有作用。我们的方法提供了新的核孔相关成分,包括位置信息,现在可以对其功能作用进行研究,以探索锥虫特异性的核篮适应、输出控制和mRNP重塑。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d12/11825100/5a892fc32b42/pbio.3003024.g001.jpg

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