Mitochondrialdysfunctionresultsindisordersthataffectonein4,000people,anddiseasesassociated withaging,suchasneurodegenerationandcancer.Improperfunctionofamitochondrialqualitycontrol process,mitophagy,aswellasmutationsinmitochondrialDNA(mtDNA)areimplicatedinthese diseases.TheroleofenvironmentalpollutantsandmitophagyintheoriginandtransmissionofmtDNA mutationsispoorlyunderstood.Theobjectiveofthisproposalistoinvestigatevariationinsusceptibility tochemical-inducedmtDNAdamageinthecontextofmitochondrialhomeostaticprocesses,howDNA damagecanleadtomtDNAmutations,andthefunctionalconsequencesofthesemutations.Themodel organismCaenorhabditiseleganshasahighlyconservedmitochondrialgenomeandwellcharacterized mitochondrialbiology,andprovidesanextremelytractablegeneticandtoxicologicalmodelforthis researchproposal.WehypothesizethatC.elegansthataregeneticallydeficientinmitophagywill accumulateandretainhigherlevelsofmtDNAdamagecomparedtowildtypeafterexposuretothe environmentaltoxicantsandknownmutagens,cadmiumandAflatoxinB1.Weproposethatthiswill increasemtDNAmutationfrequencies.Thisworkwillalsoinformtheroleofmitophagyintransmission ofmtDNAmutationsintothenextgeneration.TodetectraremtDNAmutations,wewilladaptawell- establishedandhighly-sensitivesequencingplatform,DuplexSequencing,forC.elegansforthefirst time.Thiswillfulfillasignificantgoalofthetrainingplan,whichistobecomeproficientincomputational biologyandbioinformatics.Wewillalsoinvestigatethepotentialhealtheffectsontheorganism, includingmitochondrialfunction,reproduction,andlifespanasaconsequenceofmtDNAmutations. Overall,thisresearchisimpactfulbecauseitwillprovidebetterunderstandingoftherolethatexposures toenvironmentalpollutantsandgeneticsusceptibilityplayintheorigin,signature,transmission,and effectsofmtDNAmutations.

Public Health Relevance

The effects of chemical toxicants on mitochondrial DNA mutagenesis are not well understood, nor are the processes involved in regulating the transmission of exogenous stress-induced mutations across generations. Therefore, this proposed research project aims to better understand the mechanisms involved in the origin and persistence of mitochondrial DNA mutations after exposure to environmental pollutants. As recent evidence implicates mitochondrial DNA mutations in human diseases such as cancer and neurodegenerative diseases, it is important to better understand the impact that the environment may have on public health.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Predoctoral Individual National Research Service Award (F31)
Project #
5F31ES030588-02
Application #
10092815
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Shaughnessy, Daniel
Project Start
2020-02-01
Project End
2022-01-31
Budget Start
2021-02-01
Budget End
2022-01-31
Support Year
2
Fiscal Year
2021
Total Cost
Indirect Cost
Name
Duke University
Department
Type
Schools of Medicine
DUNS #
044387793
City
Durham
State
NC
Country
United States
Zip Code
27705