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Ecology and Evolutionary Biology

Portland State University

Caenorhabditis

Articles 1 - 2 of 2

Full-Text Articles in Life Sciences

Accumulation And Transmission Dynamics Of A Naturally-Occurring Mtdna Deletion In Caenorhabditis Briggsae, Jennifer Anne Sullins Dec 2018

Accumulation And Transmission Dynamics Of A Naturally-Occurring Mtdna Deletion In Caenorhabditis Briggsae, Jennifer Anne Sullins

Dissertations and Theses

Maintaining mitochondrial genome sequence integrity is essential for preserving normal mitochondrial function. Several human diseases have been associated with heteroplasmic mitochondrial genome mutations, but few genetic systems can simultaneously represent pathogenic mitochondrial genome evolution and inheritance. The nematode Caenorhabditis briggsae is one such model. Natural C. briggsae isolates are globally-distributed and phylogenetically grouped into three distinct clades, with isolates exhibiting varying levels of a large-scale mtDNA deletion, nad5∆. Furthermore, a small subset of clade II isolates exhibits putative compensatory mutations that may reduce the risk of deletion formation and accumulation in those populations. In this thesis, the author characterizes the …


Natural Variation In Life History And Aging Phenotypes Is Associated With Mitochondrial Dna Deletion Frequency In Caenorhabditis Briggsae, Suzanne Estes, Anna Luella Coleman-Hulbert, Kiley Ann Hicks, Gene De Haan, Sarah R. Martha, Jeremiah B. Knapp, Samson William Smith, Kevin C. Stein, Dee R. Denver Jan 2011

Natural Variation In Life History And Aging Phenotypes Is Associated With Mitochondrial Dna Deletion Frequency In Caenorhabditis Briggsae, Suzanne Estes, Anna Luella Coleman-Hulbert, Kiley Ann Hicks, Gene De Haan, Sarah R. Martha, Jeremiah B. Knapp, Samson William Smith, Kevin C. Stein, Dee R. Denver

Biology Faculty Publications and Presentations

Background: Mutations that impair mitochondrial functioning are associated with a variety of metabolic and age-related disorders. A barrier to rigorous tests of the role of mitochondrial dysfunction in aging processes has been the lack of model systems with relevant, naturally occurring mitochondrial genetic variation. Toward the goal of developing such a model system, we studied natural variation in life history, metabolic, and aging phenotypes as it relates to levels of a naturally-occurring heteroplasmic mitochondrial ND5 deletion recently discovered to segregate among wild populations of the soil nematode, Caenorhabditis briggsae. The normal product of ND5 is a central component of the …