Back

How the TREX-2 complex associates with the nuclear pore

Obarska-Kosinska, A.; Zhu, Y.; Geissler, K.; Rosenkranz, R. R. E.; Yokoyama, N.; Kreysing, J. P.; Xing, H.; Glushkova, D.; Kubanska, M. A.; Böhm, S.; Kräusslich, H.-G.; Turonova, B.; Liu, F.; Beck, M.

2026-02-21 cell biology
10.64898/2026.02.20.707084 bioRxiv
Show abstract

Nuclear pore complexes (NPCs) control nucleocytoplasmic transport in eukaryotes, yet their architecture remains incompletely understood. Here we report a substantially extended structure of the human NPC, obtained by combining cryo-electron tomography, crosslinking mass spectrometry, and AI-assisted integrative modeling. We resolve the molecular arrangement of TPR, NUP153, NUP50 and ZC3HC1, and reveal that five additional proteins -- TMEM209, SMPD4, GANP, Centrin-2 and ENY2 -- are incorporated into the NPC. Unexpectedly, GANP, Centrin-2 and ENY2, core members of the TREX-2 mRNA export complex, are built into the nuclear ring. This finding establishes TREX-2 not as a transiently associated factor, but as an integral NPC module, positioning it opposite of the cytoplasmic NUP214 mRNA export platform. Together, our results redefine the molecular composition of the inner ring, nuclear ring and nuclear basket. They suggest a direct structural basis that couples TREX-2-mediated mRNP remodeling to NPC-facilitated transport.

Matching journals

The top 4 journals account for 50% of the predicted probability mass.

50% of probability mass above

"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.