The long-range objective of the proposed research is to determine the cellular and molecular events that lead to the differentiation of specific cell types in the vertebrate retina. The primary goal of the current application is to evaluate a mechanistic model for how Hedgehog (Hh) signaling and retinoic acid (RA) signaling control photoreceptor development. In this model, these signaling systems are co-regulated and act in parallel: Hh signaling propagates cone differentiation and regulates RA signaling, and RA signaling propagates rod differentiation and regulates photoreceptor phenotype. We hypothesize that Hh and RA act by influencing expression of the transcription factors crx and rxl/2, which in turn regulate photoreceptor-specific gene expression. Our research uses the zebrafish, a powerful, in vivo system for studying the mechanisms of vertebrate photoreceptor development. Through the use of genetic and molecular tools that allow the manipulation of the Hh and RA signaling systems, we will (1) identify cellular and molecular targets of Hh signaling during photoreceptor differentiation, (2) identify cellular and molecular targets of RA signaling during photoreceptor differentiation, and (3) determine the mechanism by which Hh and RA signaling are coordinated. In addition to testing these components of the mechanistic model, our experiments will determine whether Hh and RA influence photoreceptor cell fate. The mechanisms that generate multiple neuronal cell types in the correct ratios present important and challenging issues in neurobiology. The proposed research is expected to elucidate the respective roles of Hh and RA in regulating development of specific photoreceptor types in vivo. Furthermore, retinoid treatment is under active testing as a therapy for retinal disease, and Hh has been suggested as a potential treatment for specific visual disorders. An improved understanding of the mechanisms of action of Hh and RA will be valuable for reassessing current treatments, and for designing future therapies.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY012146-08
Application #
7059919
Study Section
Biology and Diseases of the Posterior Eye Study Section (BDPE)
Program Officer
Mariani, Andrew P
Project Start
1998-06-01
Project End
2008-04-30
Budget Start
2006-05-01
Budget End
2007-04-30
Support Year
8
Fiscal Year
2006
Total Cost
$280,524
Indirect Cost
Name
University of Idaho
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
075746271
City
Moscow
State
ID
Country
United States
Zip Code
83844
Patel, Jagdish Suresh; Brown, Celeste J; Ytreberg, F Marty et al. (2018) Predicting peak spectral sensitivities of vertebrate cone visual pigments using atomistic molecular simulations. PLoS Comput Biol 14:e1005974
McGinn, Timothy E; Mitchell, Diana M; Meighan, Peter C et al. (2018) Restoration of Dendritic Complexity, Functional Connectivity, and Diversity of Regenerated Retinal Bipolar Neurons in Adult Zebrafish. J Neurosci 38:120-136
Sun, Chi; Galicia, Carlos; Stenkamp, Deborah L (2018) Transcripts within rod photoreceptors of the Zebrafish retina. BMC Genomics 19:127
Sun, Chi; Mitchell, Diana M; Stenkamp, Deborah L (2018) Isolation of photoreceptors from mature, developing, and regenerated zebrafish retinas, and of microglia/macrophages from regenerating zebrafish retinas. Exp Eye Res 177:130-144
Sukeena, Joshua M; Galicia, Carlos A; Wilson, Jacob D et al. (2016) Characterization and Evolution of the Spotted Gar Retina. J Exp Zool B Mol Dev Evol 326:403-421
Stenkamp, Deborah L (2015) Development of the Vertebrate Eye and Retina. Prog Mol Biol Transl Sci 134:397-414
Mitchell, Diana M; Stevens, Craig B; Frey, Ruth A et al. (2015) Retinoic Acid Signaling Regulates Differential Expression of the Tandemly-Duplicated Long Wavelength-Sensitive Cone Opsin Genes in Zebrafish. PLoS Genet 11:e1005483
Dhakal, Susov; Stevens, Craig B; Sebbagh, Meyrav et al. (2015) Abnormal retinal development in Cloche mutant zebrafish. Dev Dyn 244:1439-1455
Kashyap, Bhavani; Pegorsch, Laurel; Frey, Ruth A et al. (2014) Eye-specific gene expression following embryonic ethanol exposure in zebrafish: roles for heat shock factor 1. Reprod Toxicol 43:111-24
Sherpa, Tshering; Lankford, Tyler; McGinn, Tim E et al. (2014) Retinal regeneration is facilitated by the presence of surviving neurons. Dev Neurobiol 74:851-76

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