? Myosins are essential for intracellular transport, and mutations in the genes encoding them have been shown to cause several inherited diseases. The characterization of the specific cellular functions of unconventional myosins has lagged behind their identification for several reasons. First, there is a great deal of redundancy within families of related myosins. Several groups have identified specific functions by expressing the cargo-binding, or tail, domains of myosins; however, this approach fails to detect any functions dependent upon prior positioning by the motor domain and can yield nonspecific effects from high levels of expression. Second, the study of mutants has been employed. Although genetic ablation approaches are very powerful, null mutants often only illuminate the initial process for which a given myosin is essential during development, precluding the identification of later physiological functions. The ultimate goal of this research is to understand the roles of myosin-Va and -Vb in multiple cellular functions. To this end, a chemical-genetic strategy has been developed that achieves selectivity, specificity, and temporal control by enlarging the ATP-binding site of the myosin using site-directed mutagenesis. This sensitizes the myosin to inhibition by a specific ADP analog while still allowing it to hydrolyze cellular ATP. The acute application of the analog then causes tight binding to actin, arresting the movement of the sensitized mutant myosin. The experiments proposed in this application will test the hypothesis that myosin-Va and myosin-Vb function in initiation, maintenance, antagonism, or termination of microtubule-based motility, using specific inhibition in HeLa, PC 12, MDCK, and B16 cell lines as well as primary cells from transgenic and knock-in mutant mice. ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM066901-02
Application #
6913684
Study Section
Synapses, Cytoskeleton and Trafficking Study Section (SYN)
Program Officer
Rodewald, Richard D
Project Start
2004-07-01
Project End
2008-06-30
Budget Start
2005-07-01
Budget End
2006-06-30
Support Year
2
Fiscal Year
2005
Total Cost
$289,275
Indirect Cost
Name
Mc Laughlin Research Institute
Department
Type
DUNS #
619471691
City
Great Falls
State
MT
Country
United States
Zip Code
59405
Wöllert, Torsten; Patel, Anamika; Lee, Ying-Lung et al. (2011) Myosin5a tail associates directly with Rab3A-containing compartments in neurons. J Biol Chem 286:14352-61
de Souza Martins, Sheila Cristina; Romao, Luciana Ferreira; Faria, Jane Cristina et al. (2009) Effect of thyroid hormone T3 on myosin-Va expression in the central nervous system. Brain Res 1275:1-9
Provance Jr, D William; Addison, Erin J; Wood, Patrick R et al. (2008) Myosin-Vb functions as a dynamic tether for peripheral endocytic compartments during transferrin trafficking. BMC Cell Biol 9:44
Salerno, Veronica P; Calliari, Aldo; Provance Jr, D William et al. (2008) Myosin-Va mediates RNA distribution in primary fibroblasts from multiple organs. Cell Motil Cytoskeleton 65:422-33
Karcher, Ryan L; Provance, D William; Gillespie, Peter G et al. (2007) Chemical-genetic inhibition of sensitized mutant unconventional myosins. Methods Mol Biol 392:231-40