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Article ; Online: TRPM7 regulates myosin IIA filament stability and protein localization by heavy chain phosphorylation.

Clark, Kristopher / Middelbeek, Jeroen / Lasonder, Edwin / Dulyaninova, Natalya G / Morrice, Nick A / Ryazanov, Alexey G / Bresnick, Anne R / Figdor, Carl G / van Leeuwen, Frank N

Journal of molecular biology

2008  Volume 378, Issue 4, Page(s) 790–803

Abstract: ... regulates myosin IIA filament stability and localization by phosphorylating a short stretch of amino acids ... we demonstrate that TRPM7 phosphorylates the COOH-termini of both mouse and human myosin IIA heavy chains ... within the alpha-helical tail of the myosin IIA heavy chain. ...

Abstract Deregulation of myosin II-based contractility contributes to the pathogenesis of human diseases, such as cancer, which underscores the necessity for tight spatial and temporal control of myosin II activity. Recently, we demonstrated that activation of the mammalian alpha-kinase TRPM7 inhibits myosin II-based contractility in a Ca(2+)- and kinase-dependent manner. However, the molecular mechanism is poorly defined. Here, we demonstrate that TRPM7 phosphorylates the COOH-termini of both mouse and human myosin IIA heavy chains--the COOH-terminus being a region that is critical for filament stability. Phosphorylated residues were mapped to Thr1800, Ser1803 and Ser1808. Mutation of these residues to alanine and that to aspartic acid lead to an increase and a decrease, respectively, in myosin IIA incorporation into the actomyosin cytoskeleton and accordingly affect subcellular localization. In conclusion, our data demonstrate that TRPM7 regulates myosin IIA filament stability and localization by phosphorylating a short stretch of amino acids within the alpha-helical tail of the myosin IIA heavy chain.
MeSH term(s) Amino Acid Sequence ; Animals ; Cell Line ; Chlorocebus aethiops ; Conserved Sequence ; Humans ; Kinetics ; Mice ; Molecular Sequence Data ; Mutation/genetics ; Myosin Heavy Chains/metabolism ; Nonmuscle Myosin Type IIA/chemistry ; Nonmuscle Myosin Type IIA/genetics ; Nonmuscle Myosin Type IIA/metabolism ; Phosphorylation ; Phosphoserine/metabolism ; Phosphothreonine/metabolism ; Sequence Alignment ; TRPM Cation Channels/genetics ; TRPM Cation Channels/metabolism
Chemical Substances TRPM Cation Channels ; Phosphothreonine (1114-81-4) ; Phosphoserine (17885-08-4) ; Nonmuscle Myosin Type IIA (EC 3.6.1.-) ; Myosin Heavy Chains (EC 3.6.4.1)
Language English
Publishing date 2008-03-04
Publishing country England
Document type Journal Article ; Research Support, Non-U.S. Gov't
ZDB-ID 80229-3
ISSN 1089-8638 ; 0022-2836
ISSN (online) 1089-8638
ISSN 0022-2836
DOI 10.1016/j.jmb.2008.02.057
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