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The official name of this gene is “actin, alpha 1, skeletal muscle.”
ACTA1 is the gene's official symbol. The ACTA1 gene is also known by other names, listed below.
The ACTA1 gene provides instructions for making a protein called skeletal alpha (α)-actin, which is part of the actin protein family. Actin proteins are important for cell movement and the tensing of muscle fibers (muscle contraction). These proteins also help maintain the cytoskeleton, which is the structural framework that determines cell shape and organizes cell contents.
Skeletal α-actin plays an important role in skeletal muscles, which are muscles that the body uses for movement. Within skeletal muscle cells, skeletal α-actin is an essential component of structures called sarcomeres. Sarcomeres are composed of thin filaments made up of actin and thick filaments made up of another protein called myosin. Attachment (binding) and release of the overlapping thick and thin filaments allows them to move relative to each other so that the muscles can contract.
At least nine mutations in the ACTA1 gene have been identified in people with actin-accumulation myopathy. Most of these mutations change single protein building blocks (amino acids) in the skeletal α-actin protein sequence.
Researchers suggest that ACTA1 gene mutations that cause actin-accumulation myopathy may affect the way the actin binds to ATP. ATP is a molecule that supplies energy for cells' activities and is important in the formation of thin filaments from individual actin molecules. Dysfunctional actin-ATP binding may result in abnormal thin filament formation and impair muscle contraction, leading to muscle weakness and the other signs and symptoms of actin-accumulation myopathy.
At least one ACTA1 gene mutation has been identified as a cause of cap myopathy. The mutation replaces the amino acid methionine with the amino acid valine at position 47 in the protein sequence, written as Met47Val or M47V. The resulting abnormal protein may interfere with the proper assembly of thin filaments. Cap myopathy is characterized by the presence of cap-like structures in muscle cells, and these structures are composed of disorganized thin filaments. The abnormal filament structure likely impairs the ability of skeletal muscles to contract, resulting in muscle weakness and the other signs and symptoms of cap myopathy.
At least seven mutations in the ACTA1 gene have been found to cause congenital fiber-type disproportion. These mutations change single amino acids in skeletal α-actin, which likely impairs the protein's ability to function normally. An altered skeletal α-actin protein disrupts muscle contraction. Inefficient muscle contraction leads to muscle weakness and the other features of congenital fiber-type disproportion.
At least 13 mutations in the ACTA1 gene have been identified in people with intranuclear rod myopathy. These mutations change single amino acids in the skeletal α-actin protein sequence.
ACTA1 gene mutations that cause intranuclear rod myopathy result in rod-shaped accumulations of actin in the nucleus of muscle cells. Normally, most actin is found in the fluid surrounding the nucleus (the cytoplasm), with small amounts in the nucleus itself. Researchers suggest that the ACTA1 gene mutations that cause intranuclear rod myopathy may interfere with the normal transport of actin between the nucleus and the cytoplasm, resulting in the accumulation of actin in the nucleus and the formation of intranuclear rods. Abnormal accumulation of actin in the nucleus of muscle cells and a corresponding reduction of available actin in muscle fibers may impair muscle contraction and lead to the muscle weakness seen in intranuclear rod myopathy.
A few ACTA1 gene mutations that have been identified in people with intranuclear rod myopathy have also been found in people with actin-accumulation myopathy. It is unclear how the same mutation can cause two different conditions.
More than 140 mutations in the ACTA1 gene have been found to cause nemaline myopathy. Nemaline myopathy is the most common muscle disorder associated with ACTA1 gene mutations. Some of the mutations that cause this disorder alter the structure or function of skeletal α-actin, causing the protein to cluster together and form clumps (aggregates). These aggregates interfere with the normal functioning of muscle cells. Other ACTA1 gene mutations prevent the production of any skeletal α-actin, impairing the muscle cells' ability to contract. ACTA1 gene mutations that cause nemaline myopathy impair muscle contraction, causing weakness and the other features of this condition.
Cytogenetic Location: 1q42.13
Molecular Location on chromosome 1: base pairs 229,431,245 to 229,434,096
The ACTA1 gene is located on the long (q) arm of chromosome 1 at position 42.13.
More precisely, the ACTA1 gene is located from base pair 229,431,245 to base pair 229,434,096 on chromosome 1.
See How do geneticists indicate the location of a gene? (http://ghr.nlm.nih.gov/handbook/howgeneswork/genelocation) in the Handbook.
You and your healthcare professional may find the following resources about ACTA1 helpful.
You may also be interested in these resources, which are designed for genetics professionals and researchers.
See How are genetic conditions and genes named? (http://ghr.nlm.nih.gov/handbook/mutationsanddisorders/naming) in the Handbook.
acids ; actin ; amino acid ; ATP ; cell ; congenital ; contraction ; cytoplasm ; cytoskeleton ; gene ; methionine ; molecule ; muscle cells ; mutation ; myosin ; nucleus ; protein ; protein sequence ; rods ; skeletal muscle ; valine
You may find definitions for these and many other terms in the Genetics Home Reference Glossary.
The resources on this site should not be used as a substitute for professional medical care or advice. Users seeking information about a personal genetic disease, syndrome, or condition should consult with a qualified healthcare professional. See How can I find a genetics professional in my area? (http://ghr.nlm.nih.gov/handbook/consult/findingprofessional) in the Handbook.