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The official name of this gene is “desmin.”
DES is the gene's official symbol. The DES gene is also known by other names, listed below.
The DES gene provides instructions for making a protein called desmin. Desmin is found in heart (cardiac) muscle and muscles used for movement (skeletal muscle). Within muscle fibers, desmin proteins are important to help maintain the structure of sarcomeres, which are necessary for muscles to tense (contract). The desmin proteins surround rod-like structures called Z-discs that are located within the sarcomere. Desmin connects the Z-discs to one another, linking neighboring sarcomeres and forming myofibrils, the basic unit of muscle fibers. The connection of sarcomeres to each other to form myofibrils is essential for maintaining muscle fiber strength during repeated cycles of contraction and relaxation.
More than 40 mutations in the DES gene have been found to cause myofibrillar myopathy. Most of these mutations change single protein building blocks (amino acids) in desmin. Mutated desmin proteins cluster together with other muscle proteins in the sarcomere to form clumps (aggregates). The aggregates prevent these proteins from functioning normally. A dysfunctional desmin protein cannot properly interact with Z-discs, leading to abnormalities of sarcomere structure and problems with the formation of myofibrils. DES gene mutations that cause myofibrillar myopathy impair the function of muscle fibers, causing weakness and the other features of this condition. People with DES gene mutations are more likely to have a weakened heart muscle (cardiomyopathy) than people with myofibrillar myopathy caused by mutations in other genes. In some cases, cardiomyopathy is the first symptom of this condition.
Mutations in the DES gene also cause a form of heart disease called dilated cardiomyopathy type 1I. This condition enlarges (dilates) and weakens the cardiac muscle, preventing it from pumping blood efficiently. DES gene mutations have also been shown to cause another form of cardiomyopathy called restrictive cardiomyopathy, in which the heart muscle is stiff and cannot fully relax after each contraction. Although cardiomyopathy is a sign of myofibrillar myopathy, these forms of cardiomyopathy are not associated with weakness of the skeletal muscles.
Mutations in the DES gene can also cause an abnormal heartbeat (arrhythmia), which may lead to heart failure and sudden death.
Researchers are not certain why some mutations in the DES gene cause these heart problems instead of myofibrillar myopathy.
Cytogenetic Location: 2q35
Molecular Location on chromosome 2: base pairs 219,418,376 to 219,426,738
The DES gene is located on the long (q) arm of chromosome 2 at position 35.
More precisely, the DES gene is located from base pair 219,418,376 to base pair 219,426,738 on chromosome 2.
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 DES 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 ; arrhythmia ; cardiac ; cardiomyopathy ; contraction ; dilated ; familial ; gene ; heart failure ; myofibrils ; protein ; sarcomere ; sign ; skeletal muscle ; symptom
You may find definitions for these and many other terms in the Genetics Home Reference Glossary (/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.