The central concept underlying this proposal is that a microtubule based motility pathway called intraflagellar transport (IFT) is critical for the assembly and maintenance of photoreceptor outer segments (OSs). IFT is a bi-directional pathway that uses the doublet microtubules of ciliary axonemes as tracks. IFT has three essential components; a large, multiprotein complex called the IFT particle, at least one plus end directed motor (ie, kinesin II), and at least one minus end directed motor (i.e., dynein 2). During the previous grant period we demonstrated the presence of all three components in vertebrate photoreceptors and established a critical role for one component (IFT88) in OS assembly. These findings suggested that IFT plays a specific role in trafficking key components of the photo-transduction system. This competing renewal is directed at determining which photo-transduction components are transported by IFT. Preliminary data showing co-isolation of the photoreceptor membrane guanylyl cyclase 1 (GC1) and rhodopsin with IFT proteins suggests the existence of IFT-cargo complexes. This proposal is directed at detailed analysis of IFT-cargo complexes than can be isolated by immunoprecipitation.
In Specific Aim 1 we will isolate hypothetical IFT-cargo complexes and determine their global composition by proteomic analysis.
In Specific Aim 2 we will test the specific hypothesis that newly synthesized OS membrane proteins (ie., GC-1, rhodopsin) associate specifically with IFT-cargo complexes using a pulse-chase paradigm with 35S-methionine.
In Specific Aim 3 we will test the hypothesis that the Dnaj chaperone, MRJ, mediates interaction of GC1 with the IFT particle using shRNA to knock-down the expression of MRJ and over expression of mutated and truncated forms of IFT88 and GC1. This will be done in stably transfected IMCD3 cells expressing photoreceptor GC1-GFP in the sensory cilium. Completion of these goals will provide molecular insight into the essential role for IFT in assembly of the photoreceptor outer segment. PUBLIC HEATH

Public Health Relevance

The photoreceptor outer segment contains hundreds of proteins that are essential for detection of light in vision. The mechanism by which the cell targets proteins necessary for vision to the outer segment are not known, but failed targeting can result in degeneration of photoreceptors and blindness. The goal of this research project is to determine the mechanism of targeting of a protein (membrane guanylyl cyclase) that when disrupted genetically leads to severe photoreceptor degeneration and blindness. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
2R01EY003222-28A2
Application #
7524179
Study Section
Biology and Diseases of the Posterior Eye Study Section (BDPE)
Program Officer
Mariani, Andrew P
Project Start
1979-09-30
Project End
2011-06-30
Budget Start
2008-07-01
Budget End
2009-06-30
Support Year
28
Fiscal Year
2008
Total Cost
$378,750
Indirect Cost
Name
Medical College of Wisconsin
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
937639060
City
Milwaukee
State
WI
Country
United States
Zip Code
53226
Lewis, Tylor R; Kundinger, Sean R; Link, Brian A et al. (2018) Kif17 phosphorylation regulates photoreceptor outer segment turnover. BMC Cell Biol 19:25
Lewis, Tylor R; Zareba, Mariusz; Link, Brian A et al. (2018) Cone myoid elongation involves unidirectional microtubule movement mediated by dynein-1. Mol Biol Cell 29:180-190
Lewis, Tylor R; Kundinger, Sean R; Pavlovich, Amira L et al. (2017) Cos2/Kif7 and Osm-3/Kif17 regulate onset of outer segment development in zebrafish photoreceptors through distinct mechanisms. Dev Biol 425:176-190
Collery, Ross F; Volberding, Peter J; Bostrom, Jonathan R et al. (2016) Loss of Zebrafish Mfrp Causes Nanophthalmia, Hyperopia, and Accumulation of Subretinal Macrophages. Invest Ophthalmol Vis Sci 57:6805-6814
Besharse, Joseph C; McMahon, Douglas G (2016) The Retina and Other Light-sensitive Ocular Clocks. J Biol Rhythms 31:223-43
Miesfeld, Joel B; Gestri, Gaia; Clark, Brian S et al. (2015) Yap and Taz regulate retinal pigment epithelial cell fate. Development 142:3021-32
Fogerty, Joseph; Besharse, Joseph C (2014) Subretinal infiltration of monocyte derived cells and complement misregulation in mice with AMD-like pathology. Adv Exp Med Biol 801:355-63
Bader, Jason R; Kusik, Brandon W; Besharse, Joseph C (2012) Analysis of KIF17 distal tip trafficking in zebrafish cone photoreceptors. Vision Res 75:37-43
Wong-Riley, Margaret T T; Besharse, Joseph C (2012) The kinesin superfamily protein KIF17: one protein with many functions. Biomol Concepts 3:267-282
Malicki, Jarema; Besharse, Joseph C (2012) Kinesin-2 family motors in the unusual photoreceptor cilium. Vision Res 75:33-6

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