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Translocation of mitochondrial DNA to the nucleus in aging

Award Number: R21AG047423
ORGANIZATION: NATIONAL INSTITUTE ON AGING
OPDIV: NIH
AWARD CLASS: DISCRETIONARY
AWARD ACTIVITY TYPE: SCIENTIFIC/HEALTH RESEARCH (INCLUDES SURVEYS)
PERIOD OF PERFORMANCE START DATE: 08/15/2014
PERIOD OF PERFORMANCE END DATE: 07/31/2016

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Translocation of mitochondrial DNA to the nucleus in aging - DESCRIPTION (provided by applicant): During evolution mitochondrial DNA (mtDNA) fragments migrated from the mitochondrial precursor organelle to the nucleus and inserted into nuclear DNA forming the eukaryotic nuclear genome. The migration process is still ongoing in many different species, leading to the disruption of nuclear genes and development of human diseases. We found in yeast the rate of mtDNA fragments migrating to the nucleus increased during the chronological life span (CLS). The CLS is determined by the survival of non-dividing cell populations. We demonstrated that yme mutants (yme; yeast mtDNA escape) with high mtDNA migration rates to the nucleus age faster, whereas mutants with decreased transfer rates live longer (ynt100-1). These phenotypes are dependent on mtDNA in mitochondria. Further, linear mtDNA fragments accumulate with likely nuclear localization in the yme1-1 mutant. The accumulation of the linear mtDNA fragments and the short CLS of the yme1-1 mutant are rescued in the absence of the non-essential DNA ligase Lig4 (Dnl4). Dnl4 is part of the non-homologous-end-joining (NHEJ) pathway, which is required for the capture of mtDNA fragments during the repair of double stranded DNA breaks in yeast. We hypothesize that linear, fragmented mtDNA enters the nucleus and accelerates aging by potentially increasing the rate of gross-chromosomal-rearrangements (GCR) and chromosome loss. The proposed project is using fibroblasts as a model system to investigate whether the findings in yeast are conserved in mammals. Several mouse and rat cell lines were created just before Hurricane Sandy struck New Jersey including the entire UMDNJ-Newark campus. Because of a 23 hours loss in electrical power supply, freezers were thawing and cell culture incubators stopped working. These conditions resulted in the loss of important mammalian cell lines. The primary purpose of this application is to regenerate these cell lines. The project should allow generating essential data which are needed to submit an R01 application, which was prevented by the caused damage of Hurricane Sandy. In aim 1 we will reconstruct mouse and rat cell lines with reduced expression of Yme1 and Lig4. This experiment has the aim to determine whether the flow of mtDNA fragments to the nucleus exists in mammals and whether it affects aging. In addition we will investigate whether mtDNA fragments insert into chromosomal DNA of fibroblasts during aging and whether that affects aging. This project should be a starting point to understand the impact of mtDNA fragments translocating to the nucleus on nuclear genomic instability and the aging process.


Issue Date FY	Funding FY	Legal Entity Name	Legal Entity Address	Legal Entity City	Legal Entity State	Legal Entity Zip Code	Legal Entity COUNTY	Legal Entity COUNTRY	Assistance Listing	Award Code	Budget Year	Action Date	Action Type	Action Amount

Issue Date FY: 2017 ( Subtotal = $0 )
2017	2014	UNIVERSITY OF MEDICINE AND DENTISTRY OF NJ (INC)							HHS Programs for Disaster Relief Appropriations Act - Non Construction	000	1	2/28/2017	NEW	$0
														Subtotal = $0

Issue Date FY: 2014 ( Subtotal = $159,000 )
2014	2014	Rutgers, The State Univ Biomedical & Health Sciences	65 Davidson Road	Piscataway	NJ	08854	MIDDLESEX	USA	HHS Programs for Disaster Relief Appropriations Act - Non Construction	000	1	8/11/2014	NEW	$159,000
														Subtotal = $159,000

Grand Total All Awards = $159,000

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Translocation of mitochondrial DNA to the nucleus in aging

Award Number: R21AG047423

ORGANIZATION: NATIONAL INSTITUTE ON AGING

OPDIV: NIH

AWARD CLASS: DISCRETIONARY

AWARD ACTIVITY TYPE: SCIENTIFIC/HEALTH RESEARCH (INCLUDES SURVEYS)

PERIOD OF PERFORMANCE START DATE: 08/15/2014

PERIOD OF PERFORMANCE END DATE: 07/31/2016

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