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Structure and function relationships in mammalian DNA polymerases

  • Nicole M. Hoitsma
  • , Amy Whitaker
  • , Matthew A. Schaich
  • , Mallory S. Smith
  • , Max S. Fairlamb
  • , Bret D. Freudenthal
  • University of Kansas

Research output: Contribution to journal › Review article › peer-review

32 Scopus citations

Abstract

DNA polymerases are vital for the synthesis of new DNA strands. Since the discovery of DNA polymerase I in Escherichia coli, a diverse library of mammalian DNA polymerases involved in DNA replication, DNA repair, antibody generation, and cell checkpoint signaling has emerged. While the unique functions of these DNA polymerases are differentiated by their association with accessory factors and/or the presence of distinctive catalytic domains, atomic resolution structures of DNA polymerases in complex with their DNA substrates have revealed mechanistic subtleties that contribute to their specialization. In this review, the structure and function of all 15 mammalian DNA polymerases from families B, Y, X, and A will be reviewed and discussed with special emphasis on the insights gleaned from recently published atomic resolution structures.

Original languageEnglish
Pages (from-to)35-59
Number of pages25
JournalCellular and Molecular Life Sciences
Volume77
Issue number1
DOIs
StatePublished - Jan 1 2020

Keywords

  • DNA polymerase
  • DNA repair
  • DNA synthesis
  • Replication
  • Structural biology

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