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Review
. 2012 Nov;13(11):687-99.
doi: 10.1038/nrm3461.

Nuclear pore complex composition: a new regulator of tissue-specific and developmental functions

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Review

Nuclear pore complex composition: a new regulator of tissue-specific and developmental functions

Marcela Raices et al. Nat Rev Mol Cell Biol. 2012 Nov.

Abstract

Nuclear pore complexes (NPCs) are multiprotein aqueous channels that penetrate the nuclear envelope connecting the nucleus and the cytoplasm. NPCs consist of multiple copies of roughly 30 different proteins known as nucleoporins (NUPs). Due to their essential role in controlling nucleocytoplasmic transport, NPCs have traditionally been considered as structures of ubiquitous composition. The overall structure of the NPC is indeed conserved in all cells, but new evidence suggests that the protein composition of NPCs varies among cell types and tissues. Moreover, mutations in various nucleoporins result in tissue-specific diseases. These findings point towards a heterogeneity in NPC composition and function. This unexpected heterogeneity suggests that cells use a combination of different nucleoporins to assemble NPCs with distinct properties and specialized functions.

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References

    1. Cell. 2008 Dec 12;135(6):1017-27 - PubMed
    1. Curr Opin Genet Dev. 2011 Aug;21(4):366-72 - PubMed
    1. Nature. 2007 Oct 4;449(7162):611-5 - PubMed
    1. Cell. 2007 Nov 2;131(3):557-71 - PubMed
    1. J Biol Chem. 2009 Oct 9;284(41):28442-28452 - PubMed

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