4.6 Review

DNA polymerase gamma, the mitochondrial replicase

Journal

ANNUAL REVIEW OF BIOCHEMISTRY
Volume 73, Issue -, Pages 293-320

Publisher

ANNUAL REVIEWS
DOI: 10.1146/annurev.biochem.72.121801.161455

Keywords

replication; fidelity; processivity; mutagenesis and disease; mitochondrial toxicity; antiviral nucleoside inhibition

Funding

  1. NHLBI NIH HHS [HL59656] Funding Source: Medline
  2. NIGMS NIH HHS [GM34042, GM45295] Funding Source: Medline
  3. NATIONAL HEART, LUNG, AND BLOOD INSTITUTE [R01HL059656] Funding Source: NIH RePORTER
  4. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R01GM045295, R01GM034042] Funding Source: NIH RePORTER

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DNA polymerase (pol) gamma is the sole DNA polymerase in animal mitochondria. Biochemical and genetic evidence document a key role for pol gamma in mitochondrial DNA replication, and whereas DNA repair and recombination were thought to be limited or absent in animal mitochondria, both have been demonstrated in recent years. Thus, the mitochondrial replicase is also apparently responsible for the relevant DNA synthetic reactions in these processes. Pol gamma comprises a catalytic core in a heterodimeric complex with an accessory subunit. The two-subunit holoenzyme is an efficient and processive polymerase, which exhibits high fidelity in nucleotide selection and incorporation while proofreading errors with its intrinsic 3' --> 5' exonuclease. Incorporation of nucleotide analogs followed by proofreading failure leads to mitochondrial toxicity in antiviral therapy, and misincorporation during DNA replication leads to mitochondrial mutagenesis and dysfunction. This review describes our current Understanding of pol gamma biochemistry and biology, and it introduces other key proteins that function at the mitochondrial DNA replication fork.

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