| Literature DB >> 19000832 |
Papia Chakraborty1, Yaming Wang, Jen-Hsuan Wei, Jan van Deursen, Hongtao Yu, Liviu Malureanu, Mary Dasso, Douglass J Forbes, David E Levy, Joachim Seemann, Beatriz M A Fontoura.
Abstract
The Nup107-160 complex, the largest subunit of the nuclear pore, is multifunctional. It mediates mRNA export in interphase, and has roles in kinetochore function, spindle assembly, and postmitotic nuclear pore assembly. We report here that the levels of constituents of the Nup107-160 complex are coordinately cell cycle-regulated. At mitosis, however, a member of the complex, Nup96, is preferentially downregulated. This occurs via the ubiquitin-proteasome pathway. When the levels of Nup96 are kept high, a significant delay in G1/S progression occurs. Conversely, in cells of Nup96(+/-) mice, which express low levels of Nup96, cell cycle progression is accelerated. These lowered levels of Nup96 yield specific defects in nuclear export of certain mRNAs and protein expression, among which are key cell cycle regulators. Thus, Nup96 levels regulate differential gene expression in a phase-specific manner, setting the stage for proper cell cycle progression.Entities:
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Year: 2008 PMID: 19000832 PMCID: PMC2835575 DOI: 10.1016/j.devcel.2008.08.020
Source DB: PubMed Journal: Dev Cell ISSN: 1534-5807 Impact factor: 12.270