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Richard J. Youle, Ph.D., Senior Investigator

Dr. Youle received an A.B. degree from Albion College and his Ph.D. degree from the University of South Carolina where he worked on the protein toxin ricin. He joined the lab of David Neville at the National Institute of Mental Health for postdoctoral work on the engineering of new cell-type-specific protein toxins. He joined the Surgical Neurology Branch of NINDS in 1985 as a principal investigator where he has developed new treatment strategies for brain tumors. His lab is now exploring the molecular mechanisms of programmed cell death and engineering therapeutic proteins to regulate cell survival.
Photo of Richard J. Youle, Ph.D., Senior Investigator

Staff:
Staff Photo for Biochemistry Section


Research Interests:
Programmed cell death. Neurons are programmed to die in great numbers during normal human development and aberrantly die by apoptosis in several neurodegenerative disorders. We are exploring the molecular mechanism of apoptosis concentrating on the roles of mitochondria and the Bcl-2 family of proteins. We have found that Bcl-xL and Bax move from the cytosol compartment to the mitochondria during apoptosis and that this step critically commits cells to the death pathway. Two major aspects of this process are under investigation; the molecular trigger for Bax migration into mitochondria and the consequences of Bax insertion into mitochondria. Live cell imaging of mitochondria and Bcl-2 family members analyzed by confocal microscopy has been instrumental in recent studies that link mitochondrial division processes to Bax mediated apoptosis. Unexpectedly, Bcl-2 family proteins have been found to regulate mitochondrial morphogenesis in healthy cells leading us to actively study the roles of mitochondrial fission and fusion especially in relation to neurodegenerative diseases.

Mitochondrial Quality Control. Mitochondria rapidly divide and fuse to form a dynamic network in cells. This process is essential for organelle quality control as evidenced by human neurodegenerative diseases caused by mutations in the genes of two large GTPases that mediate these processes. We have identified a series of E3 ligases on the outer mitochondrial membrane and are exploring how they control mitochondrial morphogenesis, protein turnover, and apoptosis.


Selected Recent Publications:
  • Youle RJ, Strasser A. (2008) The BCL-2 protein family: opposing activities that mediate cell death , Nat Rev Mol Cell Biol 9, 47-59 .

  • Norris KL, Youle RJ. (2008) Cytomegalovirus proteins vMIA and m38.5 link mitochondrial morphogenesis to Bcl-2 family proteins., J Virol 82(13), 6232-43.

  • Suen DF, Norris KL, Youle RJ. (2008) Mitochondrial dynamics and apoptosis., Genes Dev. Jun 15;22(12), 1577-90.

  • Antignani A, Youle RJ. (2008) Endosome fusion induced by diphtheria toxin translocation domain., Proc Natl Acad Sci U S A 105, 8020-5.

  • Karbowski M, Neutzner A, Youle RJ (2007) The mitochondrial E3 ubiquitin ligase MARCH5 is required for DrpI dependent mitochondrial division , J Cell Biol 178, 71-84.

  • Goyal G, Fell B, Sarin A, Youle RJ, Sriram V. (2007) Role of mitochondrial remodeling in programmed cell death in Drosophila melanogaster , Dev. Cell 12, 80716.

  • Karbowski, Norris KL, Cleland MM,Jeong SY, Youle RJ. (2006) Role of Bax and Bak in Mitochodrial Morphogenesis. , Nature 443, 658-62.

All Selected Publications


Contact Information:

Dr. Richard J. Youle
Surgical Neurology Branch, NINDS
Porter Neuroscience Research Center
Building 35, Room 2C-917
35 Convent Drive, MSC 3704
Bethesda, MD 20892-3704

Telephone: (301) 496-6628 (office), (301) 496-6628 (laboratory), (301) 402-0380 (fax)
Email: youle@helix.nih.gov

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Last updated Thursday, February 14, 2008