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J. Biol. Chem., Vol. 276, Issue 9, 6073-6082, March 2, 2001
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,
**
From the Myosin light chain phosphatase consists of three
subunits, a 38-kDa catalytic subunit, a large 110-130-kDa myosin
binding subunit, and a small subunit of 20-21 kDa. The catalytic
subunit and the large subunit have been well characterized. The small subunit has been cloned and studied from smooth muscle, but little is
known about its function and specificity in the other muscles such as
cardiac muscle. In this study, cDNAs for heart-specific small
subunit isoforms, hHS-M21, were isolated and
characterized. Evidence was obtained from an analysis of genome to
suggest that the small subunit was the product of the same gene as the
large subunit. Using permeabilized renal artery preparation and
permeabilized cardiac myocytes, it was shown that the small subunit
increased sensitivity to Ca2+ in muscle contraction. It was
also shown using an overlay assay that hHS-M21 bound the
large subunit. Mapping experiments demonstrated that the binding domain
and the domain involved in the increasing Ca2+ sensitivity
mapped to the same N-terminal region of hHS-M21. These
observations suggest that the heart-specific small subunit hHS-M21 plays a regulatory role in cardiac muscle
contraction by its binding to the large subunit.
Department of Molecular Pathogenesis,
Division of Adult Diseases, Medical Research Institute, Tokyo Medical
and Dental University, Tokyo 101-0062, the § Department of
Cardiovascular Medicine, Graduate School of Medical Sciences, Kyushu
University, Fukuoka 812-8582, the ¶ Division of Molecular
Cardiology, Research Institution of Angiocardiology, Faculty of
Medicine, Kyushu University, Fukuoka 812-8582, and the
Etiology
and Pathogenesis Research Unit, Medical Research Institute, Tokyo
Medical and Dental University, Tokyo 101-0062, Japan
The nucleotide sequence(s) reported in this paper has been submitted to the GenBankTM/EMBL Data Bank with accession number(s) AB050641 (for hHS-M21 A) and AB050642 (for hHS-M21 B).
** To whom correspondence should be addressed: Dept. of Molecular Pathogenesis, Div. of Adult Diseases, Medical Research Inst., Tokyo Medical and Dental University, 2-3-10 Kandasurugadai, Chiyoda-ku, Tokyo 101-0062, Japan. Tel.: 81-3-5280-8056; Fax: 81-3-5280-8055; E-mail: akitis@mri.tmd.ac.jp.This article has been cited by other articles:
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