Mutations and polymorphisms of the skeletal muscle a-actin gene (ACTA1)

The ACTA1 gene encodes skeletal muscle a-actin, which is the predominant actin isoform in the sarcomeric thin filaments of adult skeletal muscle, and essential, along with myosin, for muscle contraction. ACTA1 disease-causing mutations were first described in 1999, when a total of 15 mutations were...

Full description

Bibliographic Details
Main Authors: Laing, N., Dye, Danielle, Wallgren-Pettersson, C., Richard, G., Monnier, N., Lillis, S., Winder, T., Lochmüller, H., Graziano, C., Mitrani-Rosenbaum, S., Twomey, D., Sparrow, J., Beggs, A., Nowak, K.
Format: Journal Article
Published: John Wiley & Sons, Inc. 2009
Online Access:http://hdl.handle.net/20.500.11937/47755
_version_ 1848757921417003008
author Laing, N.
Dye, Danielle
Wallgren-Pettersson, C.
Richard, G.
Monnier, N.
Lillis, S.
Winder, T.
Lochmüller, H.
Graziano, C.
Mitrani-Rosenbaum, S.
Twomey, D.
Sparrow, J.
Beggs, A.
Nowak, K.
author_facet Laing, N.
Dye, Danielle
Wallgren-Pettersson, C.
Richard, G.
Monnier, N.
Lillis, S.
Winder, T.
Lochmüller, H.
Graziano, C.
Mitrani-Rosenbaum, S.
Twomey, D.
Sparrow, J.
Beggs, A.
Nowak, K.
author_sort Laing, N.
building Curtin Institutional Repository
collection Online Access
description The ACTA1 gene encodes skeletal muscle a-actin, which is the predominant actin isoform in the sarcomeric thin filaments of adult skeletal muscle, and essential, along with myosin, for muscle contraction. ACTA1 disease-causing mutations were first described in 1999, when a total of 15 mutations were known. In this article we describe 177 different disease-causing ACTA1 mutations, including 85 that have not been described before. ACTA1 mutations result in five overlapping congenital myopathies: nemaline myopathy; intranuclear rod myopathy; actin filament aggregate myopathy; congenital fiber type disproportion; and myopathy with core-like areas. Mixtures of these histopathological phenotypes may be seen in a single biopsy from one patient. Irrespective of the histopathology, the disease is frequently clinically severe, with many patients dying within the first year of life. Most mutations are dominant and most patients have de novo mutations not present in the peripheral blood DNA of either parent. Only 10% of mutations are recessive and they are genetic or functional null mutations. To aid molecular diagnosis and establishing genotype-phenotype correlations, we have developed a locus-specific database for ACTA1 variations (<a href="http://waimr.uwa.edu.au).">http://waimr.uwa.edu.au).</a> © 2009 Wiley-Liss, Inc.
first_indexed 2025-11-14T09:35:46Z
format Journal Article
id curtin-20.500.11937-47755
institution Curtin University Malaysia
institution_category Local University
last_indexed 2025-11-14T09:35:46Z
publishDate 2009
publisher John Wiley & Sons, Inc.
recordtype eprints
repository_type Digital Repository
spelling curtin-20.500.11937-477552017-09-13T14:16:24Z Mutations and polymorphisms of the skeletal muscle a-actin gene (ACTA1) Laing, N. Dye, Danielle Wallgren-Pettersson, C. Richard, G. Monnier, N. Lillis, S. Winder, T. Lochmüller, H. Graziano, C. Mitrani-Rosenbaum, S. Twomey, D. Sparrow, J. Beggs, A. Nowak, K. The ACTA1 gene encodes skeletal muscle a-actin, which is the predominant actin isoform in the sarcomeric thin filaments of adult skeletal muscle, and essential, along with myosin, for muscle contraction. ACTA1 disease-causing mutations were first described in 1999, when a total of 15 mutations were known. In this article we describe 177 different disease-causing ACTA1 mutations, including 85 that have not been described before. ACTA1 mutations result in five overlapping congenital myopathies: nemaline myopathy; intranuclear rod myopathy; actin filament aggregate myopathy; congenital fiber type disproportion; and myopathy with core-like areas. Mixtures of these histopathological phenotypes may be seen in a single biopsy from one patient. Irrespective of the histopathology, the disease is frequently clinically severe, with many patients dying within the first year of life. Most mutations are dominant and most patients have de novo mutations not present in the peripheral blood DNA of either parent. Only 10% of mutations are recessive and they are genetic or functional null mutations. To aid molecular diagnosis and establishing genotype-phenotype correlations, we have developed a locus-specific database for ACTA1 variations (<a href="http://waimr.uwa.edu.au).">http://waimr.uwa.edu.au).</a> © 2009 Wiley-Liss, Inc. 2009 Journal Article http://hdl.handle.net/20.500.11937/47755 10.1002/humu.21059 John Wiley & Sons, Inc. unknown
spellingShingle Laing, N.
Dye, Danielle
Wallgren-Pettersson, C.
Richard, G.
Monnier, N.
Lillis, S.
Winder, T.
Lochmüller, H.
Graziano, C.
Mitrani-Rosenbaum, S.
Twomey, D.
Sparrow, J.
Beggs, A.
Nowak, K.
Mutations and polymorphisms of the skeletal muscle a-actin gene (ACTA1)
title Mutations and polymorphisms of the skeletal muscle a-actin gene (ACTA1)
title_full Mutations and polymorphisms of the skeletal muscle a-actin gene (ACTA1)
title_fullStr Mutations and polymorphisms of the skeletal muscle a-actin gene (ACTA1)
title_full_unstemmed Mutations and polymorphisms of the skeletal muscle a-actin gene (ACTA1)
title_short Mutations and polymorphisms of the skeletal muscle a-actin gene (ACTA1)
title_sort mutations and polymorphisms of the skeletal muscle a-actin gene (acta1)
url http://hdl.handle.net/20.500.11937/47755