TWNK Gene

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This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/gene/twnk

Twinkle mtDNA helicase.

genes

1. Normal Function

The TWNK gene provides instructions for making two very similar proteins called Twinkle and Twinky. These proteins are found in the mitochondria, which are structures in which a process called oxidative phosphorylation occurs to convert 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. The Twinkle protein is involved in the production and maintenance of mtDNA. It functions as a mitochondrial DNA helicase, which means it binds to DNA and temporarily unwinds the two spiral strands (double helix) of the DNA molecule. This unwinding is necessary for copying (replicating) mtDNA. The function of the Twinky protein is unknown.

2. Health Conditions Related to Genetic Changes

2.1. Ataxia Neuropathy Spectrum

Mutations in the TWNK gene have been found in a small number of people with ataxia neuropathy spectrum. This condition 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 ataxia neuropathy spectrum.

Mutations in the TWNK gene disrupt the function of Twinkle and lead to large deletions of mtDNA in the muscle tissue of affected individuals. However, it is unclear how mutations in the TWNK gene cause the signs and symptoms of ataxia neuropathy spectrum.

2.2. Infantile-Onset Spinocerebellar Ataxia

At least six mutations in the TWNK gene have been found to cause infantile-onset spinocerebellar ataxia (IOSCA). The most common mutation replaces the protein building block (amino acid) tyrosine with the amino acid cysteine at position 508 in the Twinkle protein, written as Tyr508Cys or Y508C. Most affected individuals have two copies of this gene mutation in each cell. At least two additional mutations have been reported that are unique to particular families. In these cases, affected individuals have one copy of the family-specific mutation and one copy of the Tyr508Cys mutation in each cell.

The TWNK gene mutations that cause IOSCA interfere with the function of the Twinkle protein and result in reduced quantities of mtDNA (mtDNA depletion). Impaired mitochondrial function, especially in the nervous system (which requires a large amount of energy), leads to neurological dysfunction and other problems associated with IOSCA.

2.3. Perrault Syndrome

At least four TWNK gene mutations have been identified in families with Perrault syndrome, a condition characterized by hearing loss in affected males and females and abnormalities of the ovaries in affected females. The mutations involved in this condition change single amino acids in the Twinkle protein. Researchers predict that these mutations impair the helicase activity of the protein. However, it is unclear exactly how TWNK gene mutations lead to hearing problems and ovarian abnormalities in affected individuals.

2.4. Progressive External Ophthalmoplegia

At least 40 TWNK gene mutations have been identified in people with an eye condition called progressive external ophthalmoplegia. This disorder weakens the muscles that control eye movement and causes the eyelids to droop (ptosis). Researchers speculate that the mutated Twinkle protein has impaired helicase activity, which stalls the DNA replication process. Although the mechanism is unclear, replication stalling seems to result in large deletions of genetic material from mtDNA in muscle tissue. 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 may be 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.

2.5. Other Disorders

In a few families, TWNK gene mutations lead to mtDNA depletion syndrome, hepatocerebral form. People with this condition experience weak muscle tone (hypotonia), a decrease in liver function, developmental delay, seizures, and loss of sensation and weakness in the limbs (peripheral neuropathy).

3. Other Names for This Gene

C10orf2
chromosome 10 open reading frame 2
PEO1
PEO1_HUMAN
progressive external ophthalmoplegia 1 protein
T7 gp4-like protein with intramitochondrial nucleoid localization
T7-like mitochondrial DNA helicase
twinkle

References

Fratter C, Gorman GS, Stewart JD, Buddles M, Smith C, Evans J, Seller A,Poulton J, Roberts M, Hanna MG, Rahman S, Omer SE, Klopstock T, Schoser B,Kornblum C, Czermin B, Lecky B, Blakely EL, Craig K, Chinnery PF, Turnbull DM,Horvath R, Taylor RW. The clinical, histochemical, and molecular spectrum of PEO1(Twinkle)-linked adPEO. Neurology. 2010 May 18;74(20):1619-26. doi:10.1212/WNL.0b013e3181df099f.
Goffart S, Cooper HM, Tyynismaa H, Wanrooij S, Suomalainen A, Spelbrink JN.Twinkle mutations associated with autosomal dominant progressive externalophthalmoplegia lead to impaired helicase function and in vivo mtDNA replication stalling. Hum Mol Genet. 2009 Jan 15;18(2):328-40. doi: 10.1093/hmg/ddn359.
Hakonen AH, Goffart S, Marjavaara S, Paetau A, Cooper H, Mattila K, LampinenM, Sajantila A, Lönnqvist T, Spelbrink JN, Suomalainen A. Infantile-onsetspinocerebellar ataxia and mitochondrial recessive ataxia syndrome are associatedwith neuronal complex I defect and mtDNA depletion. Hum Mol Genet. 2008 Dec1;17(23):3822-35. doi: 10.1093/hmg/ddn280.
Hakonen AH, Isohanni P, Paetau A, Herva R, Suomalainen A, Lönnqvist T.Recessive Twinkle mutations in early onset encephalopathy with mtDNA depletion.Brain. 2007 Nov;130(Pt 11):3032-40.
Hudson G, Deschauer M, Busse K, Zierz S, Chinnery PF. Sensory ataxicneuropathy due to a novel C10Orf2 mutation with probable germline mosaicism.Neurology. 2005 Jan 25;64(2):371-3.
Korhonen JA, Pande V, Holmlund T, Farge G, Pham XH, Nilsson L, Falkenberg M.Structure-function defects of the TWINKLE linker region in progressive externalophthalmoplegia. J Mol Biol. 2008 Mar 28;377(3):691-705. doi:10.1016/j.jmb.2008.01.035.
Longley MJ, Humble MM, Sharief FS, Copeland WC. Disease variants of the human mitochondrial DNA helicase encoded by C10orf2 differentially alter proteinstability, nucleotide hydrolysis, and helicase activity. J Biol Chem. 2010 Sep24;285(39):29690-702. doi: 10.1074/jbc.M110.151795.
Lönnqvist T, Paetau A, Valanne L, Pihko H. Recessive twinkle mutations causesevere epileptic encephalopathy. Brain. 2009 Jun;132(Pt 6):1553-62. doi:10.1093/brain/awp045.
Morino H, Pierce SB, Matsuda Y, Walsh T, Ohsawa R, Newby M, Hiraki-Kamon K,Kuramochi M, Lee MK, Klevit RE, Martin A, Maruyama H, King MC, Kawakami H.Mutations in Twinkle primase-helicase cause Perrault syndrome with neurologicfeatures. Neurology. 2014 Nov 25;83(22):2054-61. doi:10.1212/WNL.0000000000001036.
Nikali K, Suomalainen A, Saharinen J, Kuokkanen M, Spelbrink JN, Lönnqvist T, Peltonen L. Infantile onset spinocerebellar ataxia is caused by recessivemutations in mitochondrial proteins Twinkle and Twinky. Hum Mol Genet. 2005 Oct15;14(20):2981-90.
Spelbrink JN, Li FY, Tiranti V, Nikali K, Yuan QP, Tariq M, Wanrooij S,Garrido N, Comi G, Morandi L, Santoro L, Toscano A, Fabrizi GM, Somer H, CroxenR, Beeson D, Poulton J, Suomalainen A, Jacobs HT, Zeviani M, Larsson C. Humanmitochondrial DNA deletions associated with mutations in the gene encodingTwinkle, a phage T7 gene 4-like protein localized in mitochondria. Nat Genet.2001 Jul;28(3):223-31. Erratum in: Nat Genet 2001 Sep;29(1):100.
Van Goethem G, Martin JJ, Van Broeckhoven C. Progressive externalophthalmoplegia characterized by multiple deletions of mitochondrial DNA:unraveling the pathogenesis of human mitochondrial DNA instability and theinitiation of a genetic classification. Neuromolecular Med. 2003;3(3):129-46.Review.

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Subjects: Genetics & Heredity

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Hongliu Chen

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Update Date: 23 Dec 2020

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