Spring 2012 Thematic Seminar Series, April 3, Mitochondria: Engines of Life, Drivers of Disease
Please join The Department of Biochemistry and The Evans Center on Tuesday, April 3, at 3 p.m. in Keefer Auditorium for second part of the Spring 2012 Thematic Seminar Series Mitochondria: Engines of Life, Drivers of Disease.
Douglas C. Wallace, PhD, Director, Center for Mitochondrial and Epigenomic Medicine (CMEM), Children’s Hospital of Philadelphia, and Professor, Department of Pathology and Laboratory Medicine, University of Pennsylvania will discuss “Energyomics-Energenomics: A Mitochondrial Etiology of Complex Diseases.”
Dr. Wallace has been working on human and mammalian mitochondrial genetics for 40 years. He was the first to demonstrate that mammalian cells harbored cytoplasmically inherited genes by inventing the cybrid transfer technique in the early 1970s and using this system to demonstrate that mammalian chloramphenicol resistance could be transferred from cell to cell by fusing only a cytoplasmic fragment, a cytoplast, in the absence of a nucleus. He then proceeded during the 1970s to define the rules of mammalian mitochondrial genetics, culminating in his demonstration of the maternal inheritance of the human mitochondrial DNA (mtDNA) in 1980. From this foundation, his research followed two paths: the investigation of the nature and extent of human mtDNA variation in aboriginal populations and the quest for diseases resulting from mutations in the mtDNA. The population studies revealed that mtDNA variation was unique in that it correlated highly with the ethnic and geographic origins of indigenous peoples. This ultimately led to the realization that mtDNA variation was limited by natural selection and that mtDNA variation has been the primary adaptive system for permitting people to survive and multiple in the range of different human environments. The quest for mtDNA diseases culminated in 1988 with the report by Wallace that Leber’s Hereditary Optic Neuropathy (LHON) was caused by a mtDNA missense mutation, making it the first maternally inherited mtDNA disease to be identified. Since that time, Dr. Wallace has not only shown that mtDNA mutations result in a wide range of clinical phenotypes but also that somatic mtDNA mutations are central to the aging process as well as for various age-related diseases such as Alzheimer and Huntington Disease. When the population specific mtDNA variation was compared to the frequency of common “complex” diseases it was found that ancient mtDNA variation plays a large role in predisposition to many of these diseases. Thus, mtDNA variation has now been shown to be central to both rare and common multi-system diseases.
Dr. Wallace will be guest of honor at a noon luncheon with graduate students and post docs, in W502. He will be available for conversation at a 4 pm, reception in the Evans Seminar Room, E112A.