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Novel polymerase gamma (POLG1) gene mutation in the linker domain associated with parkinsonism
© Dolhun et al.; licensee BioMed Central Ltd. 2013
Received: 13 September 2012
Accepted: 11 July 2013
Published: 18 July 2013
Mutations in the POLG1 gene have variable phenotypic presentations and a high degree of clinical suspicion is necessary for their recognition. Parkinsonism and ataxia are the most common movement disorders associated with POLG1 mutations but no phenotype-genotype correlation has been established.
We identified a male patient with progressive external ophthalmoplegia who also developed a progressive bradykinesia, rigidity and camptocormia in the third decade. Parkinsonism was partially responsive to dopaminegic replacement. His father and brother had reportedly similar clinical problems. Genetic analysis identified a novel mutation p.K512M in the POLG1 gene.
This report further expands the spectrum of POLG1-associated neurologic problems with the report of a novel mutation in the linker region of the gene, which are rarely associated with parkinsonism.
Mitochondrial DNA polymerase gamma (POLG1) is a nuclear-encoded protein critical for the synthesis, replication and repair of mitochondrial DNA (mtDNA). Abnormal function of this sole mtDNA polymerase leads to defective oxidative phosphorylation and ATP production. Impaired integrity of mtDNA with its depletion or deletion causes a broad spectrum of both non-neurological and neurological phenotypes . Greater than one hundred pathogenic mutations in this enzyme have been found since it was first described . These include, but are not limited to parkinsonism, chronic progressive external ophthalmoplegia (CPEO), cerebellar ataxia, sensory polyneuropathy, Alpers-Huttenlocher syndrome, which is characterized by progressive encephalopathy with seizures and hepatic failure, isolated myoclonic epilepsy or non-syndromic liver failure. [2–6] This wide variety of distinct and seemingly unrelated clinical problems with both autosomal dominant (AD) or recessive (AR) inheritance presents a significant challenge to clinicians and a high degree of clinical suspicion is typically crucial for the recognition of the underlying genetic mechanism. Here we report a novel mutation in POLG1 located in the linker domain of this gene in a patient with parkinsonism and CPEO.
Additional file 1: The presented patient has bilateral ptosis and facial weakness. He displays complete ophthalmoplegia when asked to move his eyes in any direction. Bilateral bradykinesia is evident. Gait is stooped and shuffling with slight anterocollis and truncal laterocollis. (MPEG 12 MB)
Parkinsonism was partially responsive to dopaminergic replacement with carbidopa/levodopa with the highest used dose of 1250 mg per day. Later, amantadine at the dose of 300 mg/day was added for his gait difficulties with reported improvement. Both medications were later reduced because of hallucinations. Dementia, treated with memantine and donepezil, was diagnosed at the age of 75 years.
Family history was positive for external ophthalmoplegia and Parkinson’s disease diagnosed in his father and brother. We could not personally examine his brother but available history indicated that he was diagnosed with Parkinson’s disease and reported a good response to 600 mg of levodopa per day.
We performed muscle biopsy because of suspicion for a mitochondrial disorder at the age of 70 years. Muscle biopsy obtained from the vastus lateralis muscle revealed nonspecific changes with some irregularities of cytochrome c-oxidase staining but ragged red fibers were not seen. These changes alone were not sufficient for the definite diagnosis of a mitochondrial myopathy. Repeat biopsy was considered with sampling of additional muscles but the patient declined. Brain MRI showed only mild scattered white matter abnormalities.
Mutations in the adenosine nucleotide translocator 1 (ANT1) and twinkle (C10ORF2) genes have also been associated with CPEO and additional neurologic problems, including parkinsonism [8, 9]. We also sequenced all coding exons of these genes using the same approach as for POLG1 analysis but no putative mutations were identified.
The presented patient reflects a significant phenotypic variability associated with mutations in the POLG1 gene. Parkinsonism is relatively rare phenotype caused by mutations in this gene. Previously suggested role of POLG1 variants as a relatively common of idiopathic Parkinson disease (PD) has not been replicated, even though it is of interest because of evidence for mitochondrial dysfunction in PD . However, the specific combination of CPEO and parkinsonism, which is partially responsive to dopaminergic therapy is occasionally seen in patients harboring POLG1 mutations. [4, 6, 11–13] Most cases with this clinical phenotype carry heterozygous mutations in the polymerase domain of the POLG1 gene and parkinsonism is a variable and inconsistent feature in these patients [4–6]. Mutations in the linker region of the POLG1gene are less common and limited data suggest that parkinsonism is more severe feature in these patients. The detected mutation p.K512M is the third known mutation in this functional domain causing CPEO and parkinsonism, together with the previously reported p.S511N and p.G517V mutations. [7, 14] We could not confirm the segregation of p.K512M mutation with the disease within this small kindred because no additional family members were available for genetic analysis, but the lysine residue at the position 512 is highly conserved and sequencing of 200 normal chromosomes did not identify this variant in a normal population (Figure 2).
Similar phenotype of CPEO and parkinsonism can be also caused by mutations in the (ANT1) and mitochondrial DNA helicase twinkle genes [8, 9]. These two genes were excluded as a potential cause of in our patient, which further strengthens the argument that the detected novel mutation in POLG1 is indeed the disease-causing mutations. We did not detect any definite signs of mitochondrial skeletal muscle myopathy in spite of severe involvement of extraocular muscles. However, other POLG1 patients with neurologic involvement and negative muscle biopsy were previously reported, suggesting that normal muscle biopsy does not exclude POLG1 mutations as a cause of multisystemic neurologic involvement .
Mutations in the POLG1 gene have emerged as another great imitator of various movement disorders and a high index of suspicion is necessary for their correct identification. Cerebellar ataxia is one of the most genetically heterogeneous movement disorders and genotype-phenotype correlations are very unreliable and the rational algorithms for the genetic testing are only emerging. A combination of external ophthalmoplegia and/or polyneuropathy was caused by POLG1 mutations in 80% of patients who tested negatively for SCA1-3, and 6, and also did not have molecular evidence for Friedreich ataxia [7, 16]. One of the most common mutations causing ataxia is p.A467T mutation that is also located in the linker domain but it causes neurologic disease only in a homozygous state. Furthermore, this mutation in a homozygous state is the most common cause of Alpers-Huttenlocher syndrome . The reasons for this variability in phenotype-genotype correlation are unknown.
Parkinsonism associated with CPEO and cerebellar ataxia associated with upgaze palsy and neuropathy are easily recognizable syndromes where mutations in the POLG1 gene should be considered. It is also important in furthering our understanding and research into the etiology of idiopathic Parkinson’s disease, particularly with regard to a possible contribution of mitochondrial dysfunction.
Written informed consent was obtained from the patient for publication of this case report and to publish the videos. Additionally, informed consent was obtained for genetic analysis. Copies of the written consent are available for review by the Editor of this journal.
We thank the patient presented here, whose help and participation made this work possible.
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