Faithful inheritance of mitochondrial DNA (mtDNA) is essential for cellular respiration and thus for most eukaryotic life. However, pathways that control mtDNA maintenance and segregation in mammalian cells are not well understood. The goal of this work is to understand the molecular mechanisms underlying the regulation of mammalian mtDNA. Once this information is known, it will be possible to identify factors that contribute to the segregation of mtDNA haplotypes that impact human health. Specifically, this proposal will address how mtDNA-protein complexes, termed nucleoids, behave in mammalian cells.
In Aim 1, super-resolution and confocal microscopy of nucleoid complexes coupled with genetic approaches to deplete and modify complex components will be employed to investigate the intracellular basis of nucleoid segregation and test the involvement of candidate effector proteins.
Aim 2 will address how the nucleoid is organized or integrated with cellular signaling pathways. This will be accomplished by systematically mapping physical and genetic interactions of the mammalian mtDNA nucleoid complex. These experiments will provide insight into the physical and functional organization of the heritable unit of mtDNA and effectively map the integrated 'interactome' of the nucleoid structure.

Public Health Relevance

Mitochondria are subcellular organelles that perform diverse and essential functions in cells. Mitochondrial DNA (mtDNA) mutations cause heritable respiratory chain deficiency and contribute to a spectrum of humans diseases, including metabolic disease, neurodegeneration, and cancer. The proposed research will elucidate mechanisms of mtDNA segregation and regulation in human cells and is relevant to the part of the NIH's mission that fosters fundamental basic cell biology discoveries that will directly lead t the identification of new therapeutic targets and therapies for the treatment of wide array of human diseases.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32GM113388-02
Application #
9062307
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Maas, Stefan
Project Start
2015-05-01
Project End
2018-04-30
Budget Start
2016-05-01
Budget End
2017-04-30
Support Year
2
Fiscal Year
2016
Total Cost
Indirect Cost
Name
University of California Davis
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
047120084
City
Davis
State
CA
Country
United States
Zip Code
95618
Lewis, Samantha C; Uchiyama, Lauren F; Nunnari, Jodi (2016) ER-mitochondria contacts couple mtDNA synthesis with mitochondrial division in human cells. Science 353:aaf5549