Successful DNA replication is essential to maintain genome integrity and prevent disease. In human cells, over 6 billion base pairs of DNA need to be replicated accurately and packaged into chromatin each cell division cycle. Furthermore, these processes must occur in the context of defects in the DNA template such as DNA damage, which present challenges to both genetic and epigenetic inheritance. The replisome is a highly regulated, dynamic machine that must work with speed and precision to duplicate the chromosomes successfully. Failures during DNA replication cause mutations, epigenetic changes, and other chromosomal aberrations that ultimately cause disease such as cancer. Our guiding hypothesis is that replication stress induces a series of DNA damage responses (DDR) that promote fork stabilization, repair, and recovery, allowing the completion of genome and chromatin replication. In this project we aim to define mechanisms that promote DNA replication especially in the context of genotoxic stress. The project uses innovative methodologies including a technology we developed called iPOND to isolate proteins on nascent DNA. Completion of this project will define DNA and chromatin replication, repair, and signaling mechanisms that act to ensure DNA replication is completed faithfully.

Public Health Relevance

Environmental and endogenous genotoxins damage DNA and challenge genome integrity. This project examines the mechanisms that maintain genome stability and prevent disease during DNA replication in the context of genotoxic stress.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21ES022319-01
Application #
8427083
Study Section
Molecular Genetics A Study Section (MGA)
Program Officer
Shaughnessy, Daniel
Project Start
2012-11-13
Project End
2014-10-31
Budget Start
2012-11-13
Budget End
2013-10-31
Support Year
1
Fiscal Year
2013
Total Cost
$234,000
Indirect Cost
$84,000
Name
Vanderbilt University Medical Center
Department
Biochemistry
Type
Schools of Medicine
DUNS #
004413456
City
Nashville
State
TN
Country
United States
Zip Code
37212
Dungrawala, Huzefa; Cortez, David (2015) Purification of proteins on newly synthesized DNA using iPOND. Methods Mol Biol 1228:123-31
Dungrawala, Huzefa; Rose, Kristie L; Bhat, Kamakoti P et al. (2015) The Replication Checkpoint Prevents Two Types of Fork Collapse without Regulating Replisome Stability. Mol Cell 59:998-1010
Sirbu, Bianca M; McDonald, W Hayes; Dungrawala, Huzefa et al. (2013) Identification of proteins at active, stalled, and collapsed replication forks using isolation of proteins on nascent DNA (iPOND) coupled with mass spectrometry. J Biol Chem 288:31458-67