Abstract
Nuclear pore complexes (NPCs) are channels that control access to the genome. The number of NPCs that cells assemble varies between different cell types and in disease. However, the mechanisms regulating NPC formation in mammalian cells remain unclear. Using a genome-wide small interfering RNA (siRNA) screen, we identify translation-related factors, proteasome components, and the CCR4-NOT complex as top regulators of NPC assembly and numbers. While inhibition of ribosomal function and protein translation reduces NPC formation, blocking protein degradation or CCR4-NOT function increases NPC numbers. We demonstrate that CCR4-NOT inhibition raises global mRNA levels, increasing the pool of nucleoporin mRNAs available for translation. Upregulation of nucleoporin complexes in CCR4-NOT-inhibited cells allows for higher NPC formation, increasing total NPC numbers in normal and cancer cells. Our findings uncover that nucleoporin mRNA stability and protein homeostasis are major determinants of NPC formation and highlight a role for the CCR4-NOT complex in negatively regulating NPC assembly.
Original language | English |
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Article number | 115468 |
Journal | Cell Reports |
Early online date | 26 Mar 2025 |
DOIs | |
State | E-pub ahead of print - 26 Mar 2025 |
Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2025 The Author(s)
Keywords
- CCR4-CNOT
- CP: Cell biology
- CP: Molecular biology
- degradation
- nuclear pore complexes
- nucleoporin
- proteostasis
- translation
ASJC Scopus subject areas
- General Biochemistry, Genetics and Molecular Biology