Major Research Areas
Researchers in the College of Graduate Studies focus their efforts where it truly matters—on the diseases and illnesses that affect many people. Much of our research activity is grouped into four areas of concentration: cancer; infectious diseases; disorders of the nervous system; and diabetes, metabolic disorders and cardiovascular diseases.
David R Mitchell, PhD
- Professor of Cell and Developmental Biology
Research Programs and Affiliations
- Biomedical Sciences Program
- Cell and Developmental Biology
Education & Fellowships
- PhD: Syracuse University, 1980
Regulation of ciliary dynein activity and assembly, and the role of the central pair complex in ciliary motility regulation.
Link to PubMed (Opens new window. Close the PubMed window to return to this page.)
Dynein and kinesin ATPases are molecular motors for many types of microtubule-based cell motility, including mitosis, directed transport of vesicles, maintenance of the endoplasmic reticulum and Golgi apparatus, and motility of (eukaryotic) cilia and flagella. We study the role of dyneins in microtubule sliding and eukaryotic flagellar bend formation, and in the regulation of flagellar waveform and beat frequency, through a combination of genetic, biochemical, and molecular approaches. While the role of dyneins as microtubule-associated motors for both ciliary and cytoplasmic motility is well recognized, little is known about their regulation or their mode of attachment to the loads they carry (vesicles or chromosomes in the cytoplasm, doublet microtubules in cilia and flagella). Our experimental system is the flagellated unicellular alga Chlamydomonas reinhardtii, since dynein subunits in Chlamydomonas flagella are homologous to subunits in mammalian dyneins but are more easily approached through genetic and molecular analyses. Human conditions that inhibit motility of these organelles (Kartagener''s syndrome, Primary Ciliary Diskinesia) are known to cause upper respiratory illnesses and male infertility. We are using in vitro mutagenesis and transformation of cloned genes to test specific hypotheses regarding the function of selected dynein subunits, and to understand mechanisms that regulate dynein assembly and activity. We are also using in vivo mutagenesis and selecting mutations that alter normal dynein function, characterizing these mutations at the molecular level, and correlating specific motility defects (analyzed by light microscopy) with defects in subunit structure and assembly. These studies provide the framework for determining general mechanisms of dynein assembly and function in all types of cell motility. The recent identification of kinesins associated with flagellar microtubules suggests that these motor proteins also play an important role in flagellar motility, and we are seeking to understand this role.
Mutations that prevent dynein assembly into flagella are also analyzed to characterize genes that are important for cytoplasmic assembly of dynein subunits, targeting to the flagellar compartment, and attachment of dynein motors to doublet microtubules. These studies will provide key information about mechanisms that regulate the intracellular distribution and activity of dyneins. Early steps in this process appear to use multiple HSP90-associated co-chaperoning complexes, but the nature of substrate recognition and the specfic steps in assembly that are helped have not been identified. Later steps involve generation of complexes that can be recognized by the transport machinery, and regulation of dynein transport into the flagellar compartment.
My favorite research organism,
Dean, A.B. and D. R. Mitchell. (2015) late steps in maturation of assembly-competent axonemal outer arm dynein in Chlamydomonas require interaction of ODA5 and ODA10 in a complex. Mol Biol Cell 26:3596-3605.
Desai, P.B., J. R. Freshour and Dr. R. Mitchell (2015) Chlamydomonas axonemal dynein assemlby locus ODA8 encodes a conserved flagellar protein needed for cytoplasmic maturation of outer dynein arm complexes. Cytoskeleton (Hoboken) 72:16-28
Dean, A.B. and D. R. Mitchell. (2013) Chlamydomonas ODA10 is a conserved axonemal protein that plays a unique role in outer dynein arm assembly. Mol Biol Cell 24:3689-3696.
Carbajal-Gonzalez, B., T. Heuser, X. Fu, J. Lin, D. R. Mitchell, B. Smith and D. Nicastro. (2013) Conserved structural motifs of the central pair complex of eukaryotic flagella. Cytoskeleton 70:101-120.
Mitchison,H.M., M. Schmidts, N.T. Loges, J. Freshour, A. Dritsoula, R.A. Hirst, C. O'Callaghan, H. Blau, M. Al Dabbagh, H. Olbrich, P.L. Beales, T. Yagi, H. Mussaffi, E.M.K. Chung, H. Omran, and D.R. Mitchell (2012) Mutations in axonemal dynein assembly factor DNAAF3 cause primary ciliary dyskinesia. Nature Genetics 44:381-389.
Hom, E.F.Y., G.B. Witman, E.H.Harris, S.K. Dutcher, R. Kamiya, D.R. Mitchell, G.J. Pazour, M.E. Porter, W.S. Sale, M. Wirschell, T. Yagi and S.M. King (2011) A unified taxonomy for ciliary dyneins. Cytosk. 68:555-565.
Gao, C., G. Wang, J. Amack and D. R. Mitchell (2010) Oda16/Wdr69 is essential for axonemal dynein assembly and ciliary motility during zebrafish embryogenesis. Developmental Dynamics 239:2190-2197.
Wei, M., P. Sivadas, H. A. Owen, D. R. Mitchell and P. Yang (2010) Chlamydomonas mutants display reversible deficiencies in flagellar beating and axonemal assembly. Cytosk. 67:71-80.
Mitchell, D. R. (2010) Polyglutamylation, the GLU that makes microtubules sticky. Current Biology 20:R234-R236.
Mitchell, D. R., and B. Smith (2009). Analysis of the central pair microtubule complex in Chlamydomonas reinhardtii. Ch. 13 In Cilia and Flagella, Part A, S. King and G. Pazour, eds., Methods in Cell Biology 92:197-213.
Duquesnoy, P., E. Escudier, L. Vincensini, J. Freshour, A-M. Bridoux, A. Coste, A. Dechildre, J. de Blic, M. Legendre, G. Montantin, H. Tenreiro, A-M. Vojtek, C. Loussert, A. Clément, D. Escalier, P. Bastin, D. R. Mitchell and S. Amselem (2009) Loss-of function mutations in the human ortholog of Chlamydomonas reinhardtii ODA7 disrupt dynein arm assembly and cause primary ciliary dyskinesia. Am. J. Hum. Genet. 85:890-896.
Satir, P., D. R. Mitchell and G. Jekely. (2008). How did the cilium evolve? Ch. 3 In: Curr. Top. Dev. Biol. Vol 85, Ciliary Function in Mammalian Development, Ed. B. K. Yoder, Elsevier, pp. 63-82.
Omran, H, D. Kobayashi, H. Olbrich, T. Tsukahara, N. T. Loges , H. Hagiwara, Q. Zhang, G. Leblond, E. O’Toole, C. Hara, H. Mizuno, H.i Kawano, M. Fliegauf, T. Yagi, S. Koshida, A. Miyawaki, H. Zentgraf, H. Seithe, R. Reinhardt, Y. Watanabe, R. Kamiya, D. R. Mitchell & H. Takeda. (2008) Ktu/PF13 is required for axonemal dynein arm formation. Nature 456:611-616.
Ahmed, N. T., C. Gao, B. J. Lucker, D. Cole, and D. R. Mitchell. (2008) ODA16 aids axonemal outer row dynein assembly through an interaction with the intraflagellar transport machinery. J. Cell Biology 183:313-322.
Wilkes, D. E., H. E. Watson, D. R. Mitchell and D. J. Asai.(2008) Twenty-five dyneins in Tetrahymena: A re-examination of the multi-dynein hypothesis. Cell Motil. Cytosk. 65:342-351.
Lindemann, C. B. and D. R. Mitchell. (2007) Evidence for axonemal distortion during the flagellar beat of Chlamydomonas. Cell Motil. Cytosk. 64:580-589.
Freshour, J., R. Yokoyama, and D. R. Mitchell.(2007) Chlamydomonas flagellar outer row dynein assembly protein Oda7 interacts with both outer row and I1 inner row dyneins. J. Biol. Chem. 282:5404-5412.
Mitchell, D. R. (2007). The evolution of eukaryotic cilia and flagella as motile and sensory organelles. Adv Exp Med Biol. 607:130-40.
Mitchell, B. F., L. B. Pedersen, M. Feely, J. L. Rosenbaum, and D. R. Mitchell. (2005) ATP production in Chlamydomonas flagella by glycolytic enzymes. Mol. Biol. Cell 16:4509-4518.
Ahmed, N. T., and D. R. Mitchell. (2005) Oda16, a highly conserved protein essential for flagellar dynein assembly and regulation. Mol. Biol. Cell 16:5004-5012.
Yokoyama, R., E. O’Toole, S. Ghosh, and D. R. Mitchell. (2004) Regulation of flagellar dynein activity by a central pair kinesin. PNAS 101:17398-17403.
Mitchell, D. R. (2004). Speculations on the evolution of 9+2 organelles and the role of central pair microtubules. Biol.Cell 96:691-696.
Mitchell, D. R., and M. Nakatsugawa. (2004) Bend propagation drives central pair rotation in Chlamydomonas reinhardtii flagella. J. Cell Biol. 166:709-715.
Zhang, H., and D. R. Mitchell. (2004) CPC1, a Chlamydomonas central pair protein with an adenylate kinase domain. J. Cell Sci. 117:4179-4188.