Thomas W Obrien
Professor Emeritus
On This Page
About Thomas W Obrien
Professor O’Brien earned his Ph.D. in physiology and biochemistry at Marquette University in 1964 for his work on the thyroid hormone control of mitochondrial content. He discovered mitochondrial ribosomes as a Postdoctoral Fellow working with Dr. G.F. Kalf. Dr. O’Brien joined the University in 1966. He was a NATO Senior Science Fellow, an EMBO Research Fellow, a Visiting Scientist at the Max Planck Institute for Molecular Genetics, Berlin, Germany, and a Visiting Scientist at the University of California Santa Cruz. From 1980 to 1982 he was Interim Chairman of our Department. From 1982 to 1987, he was founding co-Director of the Interdisciplinary Center for Biotechnology Research. Dr. O’Brien was elected as President of the Mitochondria Research Society.
Teaching Profile
Courses Taught
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IDH4917 – Undergrad Research
College of Liberal Arts and Sciences
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ALS4905 – Problems in Agricul
College of Agricultural and Life Sciences
Research Profile
Our laboratory has developed the bovine mitochondrial ribosome as a model system to address several questions related to the structure, function, biosynthesis and evolution of these interesting ribosomes. Chromosomal localization of human mitoribosomal genes is important for those mitoribosome proteins involved in genetic disease. Coordinate synthesis of the 85 different mitoribosomal proteins (nuclear gene products) with the mitochondrial ribosomal RNA (a mitochondrial gene product) is under investigation. Two of the mitochondrial ribosomal proteins, MRPS29 and MRPS30, may also may be involved in apoptosis. The mitochondrial mRNAs are highly structured and special initiation factors are required to translate these unusual messages.
Publications
Academic Articles
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Lamin AC Cardiomyopathy, the Next Masquerader: Laminopathy Mimicking Cardiac Sarcoidosis.
- Journal
- Cureus.
- Volume/Issue
- 17(3)
- [DOI]
- 10.7759/cureus.80563.
- [PMID]
- 40225500.
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The Spectrum of Pyruvate Dehydrogenase Complex Deficiency: Clinical, Biochemical and Genetic Features in 371 Patients (Vol 105, Pg 34, 2012)
- Journal
- Molecular Genetics and Metabolism.
- Volume/Issue
- 106(3):384-394
- [DOI]
- 10.1016/j.ymgme.2012.03.016.
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The spectrum of pyruvate dehydrogenase complex deficiency: clinical, biochemical and genetic features in 371 patients.
- Journal
- Molecular genetics and metabolism.
- Volume/Issue
- 105(1):34-43
- [DOI]
- 10.1016/j.ymgme.2011.09.032.
- [PMID]
- 22079328.
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Nuclear MRP genes and mitochondrial disease.
- Journal
- Gene.
- Volume/Issue
- 354:147-51
- [PMID]
- 15908146.
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Properties of human mitochondrial ribosomes.
- Journal
- IUBMB life.
- Volume/Issue
- 55(9):505-13
- [PMID]
- 14658756.
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Evolution of a protein-rich mitochondrial ribosome: implications for human genetic disease.
- Journal
- Gene.
- Volume/Issue
- 286(1):73-9
- [PMID]
- 11943462.
Contact Details
- Business:
- (352) 392-6878
- Business:
- tobrien@ufl.edu
- Business Mailing:
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PO Box 100245
GAINESVILLE FL 32610 - Business Street:
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R2237 ARB
GAINESVILLE FL 326100001