In eukaryotes, DNA polymerases (Pols) ? and ? play important roles in replication, but how these Pols contribute to the replication of the leading DNA strand has remained unclear. While the widely accepted model posits that Pol? replicates the leading strand and Pol? replicates the lagging strand, we recently published evidence that Pol? replicates both the leading and lagging DNA strands. Nevertheless, important issues pertaining to their roles in replication remain to be resolved. Here we propose a number of highly innovative ideas and experimental approaches to unambiguously establish the roles of Pol? and Pol? in replication. To determine whether Pol? or Pol? replicates the leading strand, in Aim 1 we will analyze Pol?-generated errors on the two DNA strands in genes located at different chromosomal sites and genome-wide in a number of different yeast strains, and we will also examine whether Pol?-generated errors occur on the leading stand;
in Aim 2 we will use mutations in the PCNA binding domain of Pol? and Pol? to determine whether Pol? plays a major role in replicating both DNA strands or whether Pol? replicates the leading strand, and we will carry out studies to analyze the genetic basis of the mutator phenotype of the pol2M-644G and the exonuclease defective pol2-4 Pol? mutant alleles; and in Aim 3, we will determine whether as indicated from our genetic studies, Pol? incorporates rNMPs on the leading strand during its roles in recombination and mismatch repair, and not during replication. Altogether, we expect that the proposed studies will resolve the outstanding issues relating to the role of Pols ? and ? in replication, and they will have important bearing on DNA replication and associated DNA repair processes and on the understanding of the roles of these Pols in genomic fidelity.

Public Health Relevance

The aims of this proposal are to determine the roles of DNA polymerases ? and ? in DNA replication and repair. These studies will have a crucial bearing on the understanding of DNA replication and associated DNA repair processes and on the elucidation of mechanisms that govern genomic fidelity.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM129689-03
Application #
9980963
Study Section
Molecular Genetics A Study Section (MGA)
Program Officer
Reddy, Michael K
Project Start
2018-08-07
Project End
2022-07-31
Budget Start
2020-08-01
Budget End
2021-07-31
Support Year
3
Fiscal Year
2020
Total Cost
Indirect Cost
Name
University of Texas Med Br Galveston
Department
Biochemistry
Type
Schools of Medicine
DUNS #
800771149
City
Galveston
State
TX
Country
United States
Zip Code
77555