Reference: Kilkenny ML, et al. (2012) A conserved motif in the C-terminal tail of DNA polymerase alpha tethers primase to the eukaryotic replisome. J Biol Chem 287(28):23740-7

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Abstract


The DNA polymerase alpha-primase complex forms an essential part of the eukaryotic replisome. The catalytic subunits of primase and pol alpha synthesize composite RNA-DNA primers that initiate the leading and lagging DNA strands at replication forks. The physical basis and physiological significance of tethering primase to the eukaryotic replisome via pol alpha remain poorly characterized. We have identified a short conserved motif at the extreme C terminus of pol alpha that is critical for interaction of the yeast ortholog pol1 with primase. We show that truncation of the C-terminal residues 1452-1468 of Pol1 abrogates the interaction with the primase, as does mutation to alanine of the invariant amino acid Phe(1463). Conversely, a pol1 peptide spanning the last 16 residues binds primase with high affinity, and the equivalent peptide from human Pol alpha binds primase in an analogous fashion. These in vitro data are mirrored by experiments in yeast cells, as primase does not interact in cell extracts with pol1 that either terminates at residue 1452 or has the F1463A mutation. The ability to disrupt the association between primase and pol alpha allowed us to assess the physiological significance of primase being tethered to the eukaryotic replisome in this way. We find that the F1463A mutation in Pol1 renders yeast cells dependent on the S phase checkpoint, whereas truncation of Pol1 at amino acid 1452 blocks yeast cell proliferation. These findings indicate that tethering of primase to the replisome by pol alpha is critical for the normal action of DNA replication forks in eukaryotic cells.

Reference Type
Journal Article | Research Support, Non-U.S. Gov't
Authors
Kilkenny ML, De Piccoli G, Perera RL, Labib K, Pellegrini L
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