Mechanism of Concerted RNA-DNA Primer Synthesis by the Human Primosome.

Publication Type:

Journal Article


J Biol Chem, Volume 291, Issue 19, p.10006-20 (2016)


DNA, DNA Polymerase I, DNA Primase, Humans, Multienzyme Complexes, Nucleic Acid Heteroduplexes


<p>The human primosome, a 340-kilodalton complex of primase and DNA polymerase α (Polα), synthesizes chimeric RNA-DNA primers to be extended by replicative DNA polymerases δ and ϵ. The intricate mechanism of concerted primer synthesis by two catalytic centers was an enigma for over three decades. Here we report the crystal structures of two key complexes, the human primosome and the C-terminal domain of the primase large subunit (p58C) with bound DNA/RNA duplex. These structures, along with analysis of primase/polymerase activities, provide a plausible mechanism for all transactions of the primosome including initiation, elongation, accurate counting of RNA primer length, primer transfer to Polα, and concerted autoregulation of alternate activation/inhibition of the catalytic centers. Our findings reveal a central role of p58C in the coordinated actions of two catalytic domains in the primosome and ultimately could impact the design of anticancer drugs. </p>

5EXR wild type, 5F0Q p58C-D/R-Mg, 5F0S p58C-D/R-Mn