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Nup153和TPR/巨环蛋白与TREX-2亚基相互作用,并且对于mRNA在……中依赖TREX-2的核输出至关重要。

Nup153 and TPR/Megator Interact with TREX-2 Subunits and Are Essential for TREX-2-Dependent Nuclear Export of mRNA in .

作者信息

Vdovina Yulia, Nikolenko Julia, Orlova Anastasia, Glukhova Anna, Kurshakova Maria, Fet Savva, Tvorogova Anna, Tyurin-Kuzmin Pyotr, Golovnin Anton, Georgieva Sofia, Kopytova Daria

机构信息

Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, 119991 Moscow, Russia.

Center of Genomic Sciences, Institute of Gene Biology, Russian Academy of Science, 119334 Moscow, Russia.

出版信息

Int J Mol Sci. 2025 Sep 4;26(17):8595. doi: 10.3390/ijms26178595.

Abstract

The TREX-2 complex is conserved from yeast to humans and is responsible for mRNA export from the nucleus to the cytoplasm. In yeast and humans, the TPR and Nup153 nucleoporins of the nuclear pore complex are involved in TREX-2-dependent mRNA export, but data on their involvement in this process is rather controversial. In the present work, we have studied the role of TPR and Nup153 in the TREX-2-dependent export of mRNA in . We have shown that Nup153 and TPR are required for the TREX-2-dependent export of mRNA, and their knockdown leads to mRNA accumulation in the cell nucleus. We have also demonstrated that Nup153 knockdown leads to TPR relocation to the nucleoplasm. Both nucleoporins are required for TREX-2 subunits' association with the nuclear pore. Nup153 depletion leads to the TREX-2 subunits' relocation from the nuclear pore to the nucleoplasm. The depletion of TPR leads to PCID2 relocation to the nucleoplasm and Xmas-2 retention at the nuclear pore and does not affect ENY2 redistribution. The TREX-2 subunits form several contacts with Nup153 and TPR. Hence, both nucleoporins are involved in the interaction with TREX-2 and TREX-2-dependent export in .

摘要

TREX-2复合物在从酵母到人类的生物中保守存在,负责mRNA从细胞核输出到细胞质。在酵母和人类中,核孔复合物的TPR和Nup153核孔蛋白参与依赖TREX-2的mRNA输出,但关于它们参与此过程的数据颇具争议。在本研究中,我们研究了TPR和Nup153在依赖TREX-2的mRNA输出中的作用。我们发现,Nup153和TPR是依赖TREX-2的mRNA输出所必需的,它们的敲低导致mRNA在细胞核中积累。我们还证明,Nup153敲低导致TPR重新定位到核质。两种核孔蛋白都是TREX-2亚基与核孔结合所必需的。Nup153缺失导致TREX-2亚基从核孔重新定位到核质。TPR的缺失导致PCID2重新定位到核质以及Xmas-2保留在核孔,并且不影响ENY2的重新分布。TREX-2亚基与Nup153和TPR形成多个接触点。因此,两种核孔蛋白都参与与TREX-2的相互作用以及依赖TREX-2的输出。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3951/12429265/bbcfbc483a61/ijms-26-08595-g001.jpg

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