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Mechanism and evolution of DNA primases

Journal

BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS
Volume 1804, Issue 5, Pages 1180-1189

Publisher

ELSEVIER
DOI: 10.1016/j.bbapap.2009.06.011

Keywords

Primase; Polymerase; NTP; dNTP; Mechanism; Inhibition; Counting; Fidelity; Misincorporation; Initiation

Funding

  1. NIH [GM54194, AI59764]
  2. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [R01AI059764] Funding Source: NIH RePORTER
  3. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R01GM054194] Funding Source: NIH RePORTER

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DNA primase synthesizes short RNA primers that replicative polymerases further elongate in order to initiate the synthesis of all new DNA strands. Thus, primase owes its existence to the inability of DNA polymerases to initiate DNA synthesis starting with 2 dNTPs. Here, we discuss the evolutionary relationships between the different families of primases (viral, eubacterial, archael, and eukaryotic) and the catalytic mechanisms of these enzymes. This includes how they choose an initiation site, elongate the growing primer, and then only synthesize primers of defined length via an inherent ability to count. Finally, the low fidelity of primases along with the development of primase inhibitors is described. (C) 2009 Elsevier B.V. All rights reserved.

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