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The official name of this gene is “polymerase (DNA directed), gamma.”
POLG is the gene's official symbol. The POLG gene is also known by other names, listed below.
The POLG gene provides instructions for making the active piece, called the alpha subunit, of a protein called polymerase gamma (pol γ). To be most effective, the alpha subunit attaches to two copies of another protein called the beta subunit to form pol γ. Pol γ is a DNA polymerase, which is a type of enzyme that "reads" sequences of DNA and uses them as templates to produce new DNA. These enzymes are important for copying (replicating) cells' genetic material. DNA polymerases also play critical roles in DNA repair.
Pol γ functions in mitochondria. Mitochondria are structures within cells in which a process called oxidative phosphorylation converts the energy from food into a form that cells can use. Mitochondria each contain a small amount of DNA, known as mitochondrial DNA (mtDNA), which is essential for the normal function of these structures. Pol γ is the only DNA polymerase that is active in mitochondria and that can replicate mtDNA.
There are many mutations in the POLG gene that cause Alpers-Huttenlocher syndrome. Alpers-Huttenlocher syndrome is part of a group of conditions called POLG-related disorders that have overlapping signs and symptoms affecting muscle-, nerve-, and brain-related functions. Alpers-Huttenlocher syndrome is characterized by seizures, loss of mental and movement abilities (psychomotor regression), and liver disease. The liver disease in Alpers-Huttenlocher syndrome can be brought on or made worse by valproic acid, a common treatment for seizures.
Most POLG gene mutations change single protein building blocks (amino acids) in the alpha subunit of pol γ. The mutations can have several effects on the function of pol γ. The alpha subunit may lose the ability to attach to the beta subunits to form pol γ. Alternately, mutated pol γ may be unable to bind the existing mtDNA strand to use as a template. Or, it may have a reduced ability to attract the DNA building blocks (nucleotides) that it uses to form new DNA. These effects impair DNA synthesis and may lead to insertion of the wrong nucleotide and decreased ability to fix the mistake.
The most common POLG gene mutation in Alpers-Huttenlocher syndrome replaces the amino acid alanine with the amino acid threonine at position 467 (written as Ala467Thr or A467T). This mutation blocks the ability of the alpha subunit to attach to the beta subunits and reduces pol γ's ability to synthesize DNA. The Ala467Thr mutation is also common in other POLG-related disorders. The different conditions may be determined, in part, by the mutation in the other copy of POLG, but there are still some mutation combinations that can cause more than one of the disorders. It is unclear how the same mutation can lead to different conditions.
Although the mechanism is unknown, many people with Alpers-Huttenlocher syndrome have fewer copies of mtDNA (mtDNA depletion). This abnormality is seen only in the tissues affected by the disease. MtDNA depletion leads to impaired oxidative phosphorylation and a decrease in cellular energy. These impairments affect tissues whose cells do not divide continually, such as brain, muscle, and liver. These tissues are most affected because they are more dependent on oxidative phosphorylation for energy, and impaired cells in these tissues are not generally replaced by new cells. The lack of energy supplies in these tissues could account for the signs and symptoms of Alpers-Huttenlocher syndrome.
Another condition caused by mutations in the POLG gene is ataxia neuropathy spectrum, a POLG-related disorder that is characterized by problems with coordination and balance (ataxia) and disturbances in nerve function (neuropathy). The conditions previously named mitochondrial recessive ataxia syndrome (MIRAS) and sensory ataxia neuropathy dysarthria and ophthalmoplegia (SANDO) are now included in the ataxia neuropathy spectrum.
As mentioned above, most mutations in the POLG gene change single amino acids in the alpha subunit of pol γ, and these mutations can have several effects on the function of pol γ. As a result, pol γ has a reduced ability to replicate mtDNA. The most common POLG gene mutation in ataxia neuropathy spectrum is the same as that in Alpers-Huttenlocher syndrome, Ala467Thr. It is unclear how the same mutation can lead to different disorders.
As in other POLG-related disorders, people with ataxia neuropathy spectrum typically have mtDNA depletion in the tissues affected by the condition, such as the brain. MtDNA depletion decreases the amount of energy available to the cell due to reduced oxidative phosphorylation, which may account for the signs and symptoms of ataxia neuropathy spectrum.
Childhood myocerebrohepatopathy syndrome (MCHS) is also caused by mutations in the POLG gene. MCHS is a POLG-related disorder that affects the muscles (myo-), brain (cerebro-), and liver (hepato-).
Many mutations in the POLG gene can cause MCHS. Most of these mutations change single amino acids in the alpha subunit of pol γ. These mutations reduce the activity of pol γ, decreasing mtDNA replication.
As in other POLG-related disorders, people with MCHS typically have mtDNA depletion in muscle, brain, or liver tissue. MtDNA depletion impairs oxidative phosphorylation in these tissues and decreases the energy available to the cells, which may cause the signs and symptoms of MCHS.
Mutations in the POLG gene cause another POLG-related disorder called myoclonic epilepsy myopathy sensory ataxia (MEMSA), which is characterized by recurrent seizures (epilepsy), muscle weakness (myopathy), and problems with coordination and balance (ataxia).
Most of the POLG gene mutations involved in MEMSA change single amino acids in the alpha subunit of pol γ. These mutations result in a less active form of pol γ that has a reduced ability to replicate mtDNA.
As in other POLG-related disorders, people with MEMSA typically have mtDNA depletion in affected tissues, such as muscle or brain. MtDNA depletion leads to impaired oxidative phosphorylation and decreased energy reserves in affected tissues, which may cause the signs and symptoms of MEMSA.
Mutations in the POLG gene are frequently responsible for an eye condition called progressive external ophthalmoplegia, another POLG-related disorder. This condition weakens the muscles that control eye movement and causes the eyelids to droop (ptosis).
There are at least 67 POLG gene mutations that cause progressive external ophthalmoplegia. Most POLG gene mutations change single amino acids in the alpha subunit of pol γ, which decreases the efficiency of mtDNA replication. As in another POLG-related disorder, Alpers-Huttenlocher syndrome, the most common POLG gene mutation in progressive external ophthalmoplegia is Ala467Thr. It is unclear how the same mutation can lead to different disorders.
In progressive external ophthalmoplegia, mutations in the POLG gene result in large deletions of genetic material from mtDNA in muscle tissue, rather than the overall mtDNA depletion seen in other POLG-related disorders. The reason for this difference is unknown. Researchers have not determined how deletions of mtDNA lead to the specific signs and symptoms of progressive external ophthalmoplegia, although the features of the condition are probably related to impaired oxidative phosphorylation. It has been suggested that eye muscles are commonly affected by mitochondrial defects because they are especially dependent on oxidative phosphorylation for energy.
Cytogenetic Location: 15q25
Molecular Location on chromosome 15: base pairs 89,316,304 to 89,334,794
The POLG gene is located on the long (q) arm of chromosome 15 at position 25.
More precisely, the POLG gene is located from base pair 89,316,304 to base pair 89,334,794 on chromosome 15.
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 POLG 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 ; alanine ; amino acid ; ataxia ; catalytic ; cell ; depletion ; DNA ; DNA repair ; dysarthria ; enzyme ; epilepsy ; gene ; insertion ; mitochondria ; mutation ; neuropathy ; nucleotide ; ophthalmoplegia ; oxidative phosphorylation ; phosphorylation ; protein ; psychomotor ; ptosis ; recessive ; regression ; spectrum ; subunit ; syndrome ; synthesis ; template ; threonine ; tissue
You may find definitions for these and many other terms in the Genetics Home Reference Glossary (http://www.ghr.nlm.nih.gov/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.