Human Dna2 Is a Nuclear and Mitochondrial DNA Maintenance Protein

Author:

Duxin Julien P.1,Dao Benjamin1,Martinsson Peter2,Rajala Nina2,Guittat Lionel1,Campbell Judith L.3,Spelbrink Johannes N.2,Stewart Sheila A.14

Affiliation:

1. Department of Cell Biology and Physiology

2. Institute of Medical Technology and Tampere University Hospital, Tampere, Finland

3. Braun Laboratories, California Institute of Technology, Pasadena, California

4. Department of Medicine, Washington University School of Medicine, St. Louis, Missouri 63110

Abstract

ABSTRACT Dna2 is a highly conserved helicase/nuclease that in yeast participates in Okazaki fragment processing, DNA repair, and telomere maintenance. Here, we investigated the biological function of human Dna2 (hDna2). Immunofluorescence and biochemical fractionation studies demonstrated that hDna2 was present in both the nucleus and the mitochondria. Analysis of mitochondrial hDna2 revealed that it colocalized with a subfraction of DNA-containing mitochondrial nucleoids in unperturbed cells. Upon the expression of disease-associated mutant forms of the mitochondrial Twinkle helicase which induce DNA replication pausing/stalling, hDna2 accumulated within nucleoids. RNA interference-mediated depletion of hDna2 led to a modest decrease in mitochondrial DNA replication intermediates and inefficient repair of damaged mitochondrial DNA. Importantly, hDna2 depletion also resulted in the appearance of aneuploid cells and the formation of internuclear chromatin bridges, indicating that nuclear hDna2 plays a role in genomic DNA stability. Together, our data indicate that hDna2 is similar to its yeast counterpart and is a new addition to the growing list of proteins that participate in both nuclear and mitochondrial DNA maintenance.

Publisher

American Society for Microbiology

Subject

Cell Biology,Molecular Biology

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