Nucleic Acids Research, Vol 26, Issue 11 2598-2605, Copyright © 1998 by Oxford University Press
K Piard, G Baldacci and I Tratner
We have generated proliferating cell nuclear antigen (PCNA) mutants by low
fidelity PCR and screened for lethal mutations by testing for lack of
complementation of a Schizosaccharomyces pombe strain disrupted for the
pcn1 + gene. We thus identified eight lethal mutants out of the 50 cDNAs
tested. Six were truncated in their C-terminal region due to the
introduction of a stop codon within their coding sequences. Two were
full-length with a single point mutation at amino acid 68 or 69. The two
latter mutants were overexpressed in insect cells via a recombinant
baculovirus and were purified. They were unable to stimulate DNA polymerase
delta DNA replication activity on a poly(dA).oligo(dT) template.
Cross-linking experiments showed that this was due to their inability to
form trimers. Since these two mutations are adjacent and not located in a
domain of the protein putatively involved in inter- monomer interactions,
our results show that the beta-sheet betaF1 to which they belong must play
an essential role in maintaining the 3- dimensional structure of S.pombe
PCNA.
ARTICLES
Single point mutations located outside the inter-monomer domains abolish trimerization of Schizosaccharomyces pombe PCNA
UPR9044, IFC1/CNRS, 7 rue Guy Moquet, 94801 Villejuif, France.
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