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Mol Biol Cell. 2013 Apr;24(8):1208-21. doi: 10.1091/mbc.E12-06-0450. Epub 2013 Feb 20.

Regulation of mRNA export by the PI3 kinase/AKT signal transduction pathway.

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1
Department of Cell and Developmental Biology, University of Massachusetts Medical School, Worcester, MA 01655, USA.

Abstract

UAP56, ALY/REF, and NXF1 are mRNA export factors that sequentially bind at the 5' end of a nuclear mRNA but are also reported to associate with the exon junction complex (EJC). To screen for signal transduction pathways regulating mRNA export complex assembly, we used fluorescence recovery after photobleaching to measure the binding of mRNA export and EJC core proteins in nuclear complexes. The fraction of UAP56, ALY/REF, and NXF1 tightly bound in complexes was reduced by drug inhibition of the phosphatidylinositide 3-kinase (PI3 kinase)/AKT pathway, as was the tightly bound fraction of the core EJC proteins eIF4A3, MAGOH, and Y14. Inhibition of the mTOR mTORC1 pathway decreased the tight binding of MAGOH. Inhibition of the PI3 kinase/AKT pathway increased the export of poly(A) RNA and of a subset of candidate mRNAs. A similar effect of PI3 kinase/AKT inhibition was observed for mRNAs from both intron-containing and intronless histone genes. However, the nuclear export of mRNAs coding for proteins targeted to the endoplasmic reticulum or to mitochondria was not affected by the PI3 kinase/AKT pathway. These results show that the active PI3 kinase/AKT pathway can regulate mRNA export and promote the nuclear retention of some mRNAs.

PMID:
23427269
PMCID:
PMC3623641
DOI:
10.1091/mbc.E12-06-0450
[Indexed for MEDLINE]
Free PMC Article
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