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Human Molecular Genetics Advance Access originally published online on December 12, 2008
Human Molecular Genetics 2009 18(5):978-987; doi:10.1093/hmg/ddn425
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© The Author 2008. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

Mutually exclusive binding of PP1 and RNA to AKAP149 affects the mitochondrial network

Marie Rogne1, Anne Jorunn Stokka2, Kjetil Taskén2, Philippe Collas1 and Thomas Küntziger1,*

1 Institute of Basic Medical Sciences, Department of Biochemistry 2 Biotechnology Centre of Oslo, University of Oslo, Post Box 1112, Blindern, 0317 Oslo, Norway

* To whom correspondence should be addressed. Tel: +47 22851064; Fax: +47 22851058; Email: t.m.kuntziger{at}medisin.uio.no

Received October 16, 2008; Accepted December 10, 2008

A-kinase-anchoring protein 149 (AKAP149) is a membrane protein of the mitochondrial and endoplasmic reticulum/nuclear envelope network. AKAP149 controls the subcellular localization and temporal order of protein phosphorylation by tethering protein kinases and phosphatases to these compartments. AKAP149 also includes an RNA-binding K homology (KH) domain, the loss of function of which has been associated in other proteins with neurodegenerative syndromes. We show here that protein phosphatase 1 (PP1) binding occurs through a conserved RVXF motif found in the KH domain of AKAP149 and that PP1 and RNA binding to this same site is mutually exclusive and controlled through a novel, phosphorylation-dependent mechanism. A collapse of the mitochondrial network is observed upon introduction of RNA-binding deficient mutants of AKAP149, pointing to the importance of RNA tethering to the mitochondrial membrane by AKAP149 for mitochondrial distribution.


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