SAC3 May Link Nuclear Protein Export to Cell Cycle Progression

Selective movement of proteins between the nucleus and the cytoplasm is a regulatory mechanism exploited extensively by the eukaryotic cell. We have identified the evolutionarily conserved Sac3 protein, which was implicated previously in the regulation of mitosis [Bauer, A. & Kolling, R. (1996)...

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Veröffentlicht in:Proceedings of the National Academy of Sciences - PNAS 2000-03, Vol.97 (7), p.3224-3229
Hauptverfasser: Jones, Amy L., Quimby, B. Booth, Hood, Jennifer K., Ferrigno, Paul, Keshava, Praveen H., Silver, Pamela A., Corbett, Anita H.
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Sprache:eng
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Zusammenfassung:Selective movement of proteins between the nucleus and the cytoplasm is a regulatory mechanism exploited extensively by the eukaryotic cell. We have identified the evolutionarily conserved Sac3 protein, which was implicated previously in the regulation of mitosis [Bauer, A. & Kolling, R. (1996) J. Cell Sci. 109, 1575-1583] as a novel mediator of nuclear protein export. We show that Sac3p is localized to the nuclear pore, where it interacts with nucleoporins. Loss of SAC3 function results in a block in nuclear export of a nuclear export signal-containing reporter protein. Our results also demonstrate that SAC3 interacts genetically with the nuclear protein export factors Crm1p/Xpo1p and Yrb2p. Taken together, these data indicate a link between nuclear protein export and transition through the cell cycle.
ISSN:0027-8424
1091-6490
DOI:10.1073/pnas.97.7.3224