Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria.

Journal article

The gene products involved in mammalian mitochondrial DNA (mtDNA) maintenance and organization remain largely unknown. We report here a novel mitochondrial protein, Twinkle, with structural similarity to phage T7 gene 4 primase/helicase and other hexameric ring helicases. Twinkle colocalizes with mtDNA in mitochondrial nucleoids. Screening of the gene encoding Twinkle in individuals with autosomal dominant progressive external ophthalmoplegia (adPEO), associated with multiple mtDNA deletions, identified 11 different coding-region mutations co-segregating with the disorder in 12 adPEO pedigrees of various ethnic origins. The mutations cluster in a region of the protein proposed to be involved in subunit interactions. The function of Twinkle is inferred to be critical for lifetime maintenance of human mtDNA integrity.

Authors: Spelbrink, J; Li, F; Tiranti, V; Nikali, K; Yuan, Q

• Publication status: Published
• Journal: Nature genetics
• Volume: 28
• Issue: 3
• Pages: 223-231
• Publication date: 2001-07-01
• DOI: 10.1038/90058
• EISSN: 1546-1718
• ISSN: 1061-4036
• Language: English
• Keywords: Amino Acid Sequence; DNA Primase; Finland; Sequence Deletion; DNA Helicases; Pedigree; Chromosomes, Human, Pair 10; Ophthalmoplegia, Chronic Progressive External; Genetic Linkage; Mutation; Heterozygote; Humans; Female; Pakistan; Cell Compartmentation; Molecular Sequence Data; Protein Conformation; Sequence Homology, Amino Acid; Italy; Protein Transport; Male; DNA, Mitochondrial