Novel familial dilated cardiomyopathy mutation in MYL2 affects the structure and function of myosin regulatory light chain. (16th April 2015)

• Record Type: Journal Article
• Authors: Huang, Wenrui; Liang, Jingsheng; Yuan, Chen‐Ching; Kazmierczak, Katarzyna; Zhou, Zhiqun; Morales, Ana; McBride, Kim L.; Fitzgerald‐Butt, Sara M.; Hershberger, Ray E.; Szczesna‐Cordary, Danuta
• Is Part Of: FEBS journal. Volume 282:Number 12(2015)
• Page Start: 2379
• Page End: 2393
• Publication Date: 2015-04-16
• Subjects: Biochemistry -- Periodicals; Molecular biology -- Periodicals; Pathology, Molecular -- Periodicals; 572
• DOI: 10.1111/febs.13286
• Languages: English
• ISSNs: 1742-464X

Abstract

<abstract abstract-type="main" id="febs13286-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Dilated cardiomyopathy (DCM) is a disease of the myocardium characterized by left ventricular dilatation and diminished contractile function. Here we describe a novel DCM mutation in the myosin regulatory light chain (RLC), in which aspartic acid at position 94 is replaced by alanine (D94A). The mutation was identified by exome sequencing of three adult first‐degree relatives who met formal criteria for idiopathic DCM. To obtain insight into the functional significance of this pathogenic <italic>MYL2</italic> variant, we cloned and purified the human ventricular RLC wild‐type (WT) and D94A mutant proteins, and performed <italic>in vitro</italic> experiments using RLC‐mutant or WT‐reconstituted porcine cardiac preparations. The mutation induced a reduction in the α‐helical content of the RLC, and imposed intra‐molecular rearrangements. The phosphorylation of RLC by Ca<sup>2+</sup>/calmodulin‐activated myosin light chain kinase was not affected by D94A. The mutation was seen to impair binding of RLC to the myosin heavy chain, and its incorporation into RLC‐depleted porcine myosin. The actin‐activated ATPase activity of mutant‐reconstituted porcine cardiac myosin was significantly higher compared with ATPase of wild‐type. No changes in the myofibrillar ATPase–pCa relationship were observed in wild‐type‐ or D94A‐reconstituted preparations. Measurements of contractile force showed a slightly reduced maximal tension per cross‐section of muscle, with no change in the calcium sensitivity of force in D94A‐reconstituted skinned porcine papillary muscle strips compared with wild‐type. Our data indicate that subtle structural rearrangements in the RLC molecule, followed by its impaired interaction with the myosin heavy chain, may trigger functional abnormalities contributing to the DCM phenotype.</p> </abstract>