Title

M20, the small subunit of PP1M, binds to microtubules

UMMS Affiliation

Department of Physiology and Biomedical Imaging Group

Publication Date

10-22-2002

Document Type

Article

Subjects

Animals; Binding Sites; COS Cells; Chick Embryo; Eukaryotic Cells; Green Fluorescent Proteins; Holoenzymes; Luminescent Proteins; Microscopy, Electron; Microtubule Proteins; Microtubules; Myosin-Light-Chain Phosphatase; Peptide Fragments; Phosphoprotein Phosphatase; Protein Binding; Protein Structure, Tertiary; Recombinant Fusion Proteins

Disciplines

Life Sciences | Medicine and Health Sciences

Abstract

Myosin light chain phosphatase (PP1M) is composed of three subunits, i.e., M20, MBS, and a catalytic subunit. Whereas MBS is assigned as a myosin binding subunit, the function of M20 is unknown. In the present study, we found that M20 binds to microtubules. The binding activity was revealed by cosedimentation of M20 with microtubules and binding of tubulin to M20 affinity resin. Green fluorescent protein (GFP)-tagged M20 (M20-GFP) was expressed in chicken primary smooth muscle cells and COS-7 cells and was used as a probe for studying the association between M20 and microtubules in living cells. M20-GFP was localized on filamentous structures in both cell types. Colocalization analysis revealed that M20-GFP colocalized with tubulin. Treatment with nocodazole, but not cytochalasin B, abolished the filamentous structure of M20-GFP. These results indicate that M20-GFP associates with microtubules in cells. Microinjection of rhodamine-tubulin into the M20-expressing cells revealed that incorporation of rhodamine-tubulin into microtubules was significantly facilitated by microtubule-associated M20. Consistent with this result, M20 enhanced the rate of tubulin polymerization in vitro and produced elongated microtubules. These results suggest that M20 has a microtubule binding activity and plays a role in regulating microtubule dynamics.

Rights and Permissions

Citation: Am J Physiol Cell Physiol. 2003 Feb;284(2):C250-62. Epub 2002 Sep 18. Link to article on publisher's site

DOI of Published Version

10.1152/ajpcell.00153.2002

Journal/Book/Conference Title

American journal of physiology. Cell physiology

Related Resources

Link to article in PubMed

PubMed ID

12388116