This is a re-submission of a competitive renewal application for the continuation of a more than twenty year old project to study DNA alkylation repair in eukaryotic cells. We propose to explore how one particular DNA repair pathway, namely base excision repair (BER) initiated by the alkyladenine DNA glycosylase repair enzyme (Aag in mice, AAG in humans;a.k.a. Mpg/MPG and Apng/APNG), contributes to the response of different cell types upon exposure to DNA damaging agents. Alkylating agents are cytotoxic, mutagenic, clastogenic, teratogenic and carcinogenic, and they represent one of the most potent and abundant classes of chemical DNA damaging agents in our environment. In addition, alkylating agents are present inside cells as normal cellular metabolites, and they are produced as byproducts of oxidative stress. Moreover, some of the most toxic alkylating agents are commonly used for the chemotherapeutic treatment of cancer patients. In the past funding period one of the most important things we learned (in addition to identifying a number of new pathways involved in protecting cells against alkylating agents) is that in certain cell types, expression of the Aag DNA repair enzyme, even at wild type levels, has the counter-intuitive consequence of rendering those cells extremely sensitive to the cytotoxic effects of DNA alkylation damage. In the next funding period we will seek to understand more fully what features of these specific cell types render Aag-initiated DNA repair so detrimental to cell survival. This will be achieved by pursuing the following four Specific Aims:
Aims 1, 2 and 3 will exploit recent advances in the stem cell/regenerative medicine field for the in vitro differentiatin of mouse embryonic stem (ES) cells into specifically differentiated hematopoietic myeloid cells, retinal photoreceptor cells, and cerebellar granule cells, all of which display Aag-dependent alkylation sensitivity in vivo, unlike their ES cell progenitor that displays Aag-dependent alkylation resistance. In addition, as part of Aims 1 and 3, we will directly isolate differentiatig and differentiated cells from mice. All cell types will be tested for their sensitivity to two diffrent alkylating agents, and one non-alkylating agent, ultraviolet light. By isolating and characterizing (Aim 4) these isogenic cells whose phenotype has transitioned from Aag-dependent alkylation resistance (ES cells) to Aag-dependent alkylation sensitivity (myeloid, photoreceptor and granule neuron cells) we hope to learn how to better predict how cells and people will respond to alkylating agents ubiquitously present in the environment, and commonly used in the clinic. The health relatedness of the proposed project is that the information gained will contribute to furthering our goals to prevent cancer and other DNA damage-related diseases, while also contributing to improving how those diseases, especially cancer, are treated in the clinic.

Public Health Relevance

The DNA that makes up the genetic material of all living organisms is constantly under attack from normal physiological processes and from both natural and manmade components of our environment. If the resulting DNA damage is left un-repaired detrimental health consequences, such as cancer, tissue degeneration and premature aging, are inevitable;despite this, DNA damaging agents are used as cancer chemotherapy agents in the hope of killing fast growing tumor cells more efficiently than healthy normal cells. For these reasons we propose to explore how one particular DNA repair pathway contributes to the response of cells, tissues and whole animals upon exposure to the commonly encountered class of DNA damaging agent, alkylating agents.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Research Project (R01)
Project #
5R01ES022872-22
Application #
8682890
Study Section
Cancer Etiology Study Section (CE)
Program Officer
Shaughnessy, Daniel
Project Start
2013-06-10
Project End
2018-02-28
Budget Start
2014-03-01
Budget End
2015-02-28
Support Year
22
Fiscal Year
2014
Total Cost
$336,001
Indirect Cost
$113,251
Name
Massachusetts Institute of Technology
Department
None
Type
Organized Research Units
DUNS #
001425594
City
Cambridge
State
MA
Country
United States
Zip Code
02139
Meira, Lisiane B; Calvo, Jennifer A; Shah, Dharini et al. (2014) Repair of endogenous DNA base lesions modulate lifespan in mice. DNA Repair (Amst) 21:78-86
Mazumder, Aprotim; Pesudo, Laia Quiros; McRee, Siobhan et al. (2013) Genome-wide single-cell-level screen for protein abundance and localization changes in response to DNA damage in S. cerevisiae. Nucleic Acids Res 41:9310-24
Svensson, J Peter; Quiros Pesudo, Laia; McRee, Siobhan K et al. (2013) Genomic phenotyping by barcode sequencing broadly distinguishes between alkylating agents, oxidizing agents, and non-genotoxic agents, and reveals a role for aromatic amino acids in cellular recovery after quinone exposure. PLoS One 8:e73736