Title

p116Rip decreases myosin II phosphorylation by activating myosin light chain phosphatase and by inactivating RhoA

UMMS Affiliation

Department of Physiology

Publication Date

11-17-2004

Document Type

Article

Subjects

Adaptor Proteins, Signal Transducing; Animals; COS Cells; Catalysis; DNA, Complementary; Dose-Response Relationship, Drug; Electrophoresis, Polyacrylamide Gel; Enzyme Activation; Escherichia coli; GTP Phosphohydrolases; Gene Silencing; Guanosine Triphosphate; Hela Cells; Humans; Hydrolysis; Microscopy, Fluorescence; Models, Biological; Molecular Sequence Data; Muscle, Smooth; Myosin-Light-Chain Phosphatase; Myosins; Phosphoric Monoester Hydrolases; Phosphorylation; Protein Binding; Protein Structure, Tertiary; RNA, Small Interfering; Signal Transduction; Temperature; Two-Hybrid System Techniques; Xenopus; rhoA GTP-Binding Protein

Disciplines

Life Sciences | Medicine and Health Sciences

Abstract

p116Rip was originally found to be a RhoA-binding protein, but its function has been unknown. Here, we clarify the function of p116Rip. Two critical findings were made. First, we found that p116Rip activated the GTPase activity of RhoA in vitro and that p116Rip overexpression in cells consistently diminished the epidermal growth factor-induced increase in GTP-bound RhoA. Second, p116Rip activated the myosin light chain phosphatase (MLCP) activity of the holoenzyme. p116Rip did not activate the catalytic subunit alone, indicating that the activation is due to the binding of p116Rip to the myosin phosphatase targeting subunit MYPT1. Interestingly, the activation of phosphatase was specific to myosin as substrate, and p116Rip directly bound to myosin, thus facilitating myosin/MLCP interaction. The gene silencing of p116Rip consistently and significantly increased myosin phosphorylation as well as stress fiber formation in cells. Based upon these findings, we propose that p116Rip is an important regulatory component that controls the RhoA signaling pathway, thus regulating MLCP activity and myosin phosphorylation in cells.

Rights and Permissions

Citation: J Biol Chem. 2005 Feb 11;280(6):4983-91. Epub 2004 Nov 14. Link to article on publisher's site

Related Resources

Link to Article in PubMed

Journal/Book/Conference Title

The Journal of biological chemistry

PubMed ID

15545284