Abstract

BackgroundDNA replication requires contributions from various proteins, such as DNA helicases; in mitochondria Twinkle is important for maintaining and replicating mitochondrial DNA. Twinkle helicases are predicted to also possess primase activity, as has been shown in plants; however this activity appears to have been lost in metazoans. Given this, the study of Twinkle in other organisms is required to better understand the evolution of this family and the roles it performs within mitochondria.ResultsHere we describe the characterization of a Twinkle homologue, Twm1, in the amoeba Dictyostelium discoideum, a model organism for mitochondrial genetics and disease. We show that Twm1 is important for mitochondrial function as it maintains mitochondrial DNA copy number in vivo. Twm1 is a helicase which unwinds DNA resembling open forks, although it can act upon substrates with a single 3′ overhang, albeit less efficiently. Furthermore, unlike human Twinkle, Twm1 has primase activity in vitro. Finally, using a novel in bacterio approach, we demonstrated that Twm1 promotes DNA replication.ConclusionsWe conclude that Twm1 is a replicative mitochondrial DNA helicase which is capable of priming DNA for replication. Our results also suggest that non-metazoan Twinkle could function in the initiation of mitochondrial DNA replication. While further work is required, this study has illuminated several alternative processes of mitochondrial DNA maintenance which might also be performed by the Twinkle family of helicases.

Highlights

  • DNA replication requires contributions from various proteins, such as DNA helicases; in mitochondria Twinkle is important for maintaining and replicating mitochondrial DNA

  • We describe the characterization of a Twinkle homologue (Twm1) in D. discoideum, encoded by the nuclear twm1 gene and targeted to mitochondria

  • D. discoideum Twm1 localizes to mitochondria A gene encoding a putative Twinkle homologue in D. discoideum was previously identified by Shutt and Gray [10]

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Summary

Introduction

DNA replication requires contributions from various proteins, such as DNA helicases; in mitochondria Twinkle is important for maintaining and replicating mitochondrial DNA. Harman and Barth BMC Molecular Biol (2018) 19:12 hexamers to unwind dsDNA at the replication fork [3, 4] Due to this structure, replicative helicases often require a loader protein to allow for the unwinding of DNA with no free 5′ end, which is typically the case for mtDNA [5, 6]. Deletion of the T7 gp linker region (located between the primase and helicase domains) results in inefficient loading of the ring-shaped hexamer on DNA [8], which could apply to Twinkle This linker region is important for the proper function and hexamerization of Twinkle [9]

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