Details

Autor(en) / Beteiligte

• Kaliszewska, Magdalena
• Kruszewski, Jakub
• Kierdaszuk, Biruta
• Kostera-Pruszczyk, Anna
• Nojszewska, Monika
• Łusakowska, Anna
• Vizueta, Joel
• Sabat, Dorota
• Lutyk, Dorota
• Lower, Michał
• Piekutowska-Abramczuk, Dorota
• Kaniak-Golik, Aneta
• Pronicka, Ewa
• Kamińska, Anna
• Bartnik, Ewa
• Golik, Paweł
• Tońska, Katarzyna

Titel

Yeast model analysis of novel polymerase gamma variants found in patients with autosomal recessive mitochondrial disease

Ist Teil von

• Human genetics, 2015-09, Vol.134 (9), p.951-966

Ort / Verlag

Berlin/Heidelberg: Springer Berlin Heidelberg

Erscheinungsjahr

2015

Link zum Volltext

Quelle

SpringerLink

Beschreibungen/Notizen

• Replication of the mitochondrial genome depends on the single DNA polymerase (pol gamma). Mutations in the POLG gene, encoding the catalytic subunit of the human polymerase gamma, have been linked to a wide variety of mitochondrial disorders that show remarkable heterogeneity, with more than 200 sequence variants, often very rare, found in patients. The pathogenicity and dominance status of many such mutations remain, however, unclear. Remarkable structural and functional conservation of human POLG and its S. cerevisiae ortholog (Mip1p) led to the development of many successful yeast models, enabling to study the phenotype of putative pathogenic mutations. In a group of patients with suspicion of mitochondrial pathology, we identified five novel POLG sequence variants, four of which (p.Arg869Ter, p.Gln968Glu, p.Thr1053Argfs*6, and p.Val1106Ala), together with one previously known but uncharacterised variant (p.Arg309Cys), were amenable to modelling in yeast. Familial analysis indicated causal relationship of these variants with disease, consistent with autosomal recessive inheritance. To investigate the effect of these sequence changes on mtDNA replication, we obtained the corresponding yeast mip1 alleles (Arg265Cys, Arg672Ter, Arg770Glu, Thr809Ter, and Val863Ala, respectively) and tested their effect on mitochondrial genome stability and replication fidelity. For three of them (Arg265Cys, Arg672Ter, and Thr809Ter), we observed a strong, partially dominant phenotype of a complete loss of functional mtDNA, whereas the remaining two led to partial mtDNA depletion and significant increase in point mutation frequencies. These results show good correlation with the severity of symptoms observed in patients and allow to establish these variants as pathogenic mutations.