Photoreceptors are the highly specialized sensory neurons that carry out the first step in vision. The mechanisms for the production of photoreceptors during development are of interest from both a basic science and a therapeutic viewpoint. Photoreceptors, particularly rods, the cells that mediate vision in dim light, are the cell type most often directly affected by genetic diseases that lead to blindness. Cone photoreceptors, which mediate our daylight and color vision, also die due to genetic and environmental causes. Replacement of dying photoreceptor cells will require knowledge of the mechanisms of their genesis. For example, stem cells can be instructed to produce rods and/or cones prior to engraftment. In addition, an understanding of photoreceptor development might lead to interventions that prevent developmental abnormalities, which lead to blindness. We propose to investigate the mechanisms by which photoreceptors are generated. The focus will be on the transcription factors that are required for photoreceptor production, including an analysis of their upstream regulators and downstream targets. State-of-the-art nucleic acid technologies that build on our previous genomic studies, as well as our newly developed methods for the study of gene regulation, will be carried out.

Public Health Relevance

Photoreceptors are the highly specialized sensory neurons that carry out the first step in vision. They are often the target of genetic diseases that lead to blindness. We propose to study the mechanisms for the production of photoreceptors, which can lead to the prevention of developmental abnormalities and/or therapies employing engraftment of photoreceptor cells produced by stem cells.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY009676-18
Application #
7888252
Study Section
Biology and Diseases of the Posterior Eye Study Section (BDPE)
Program Officer
Greenwell, Thomas
Project Start
1992-08-01
Project End
2012-06-30
Budget Start
2010-07-01
Budget End
2012-06-30
Support Year
18
Fiscal Year
2010
Total Cost
$412,035
Indirect Cost
Name
Harvard University
Department
Genetics
Type
Schools of Medicine
DUNS #
047006379
City
Boston
State
MA
Country
United States
Zip Code
02115
Mizeracka, Karolina; DeMaso, Christina R; Cepko, Constance L (2013) Notch1 is required in newly postmitotic cells to inhibit the rod photoreceptor fate. Development 140:3188-97
Emerson, Mark M; Surzenko, Natalia; Goetz, Jillian J et al. (2013) Otx2 and Onecut1 promote the fates of cone photoreceptors and horizontal cells and repress rod photoreceptors. Dev Cell 26:59-72
Mizeracka, Karolina; Trimarchi, Jeffrey M; Stadler, Michael B et al. (2013) Analysis of gene expression in wild-type and Notch1 mutant retinal cells by single cell profiling. Dev Dyn 242:1147-59
Emerson, Mark M; Cepko, Constance L (2011) Identification of a retina-specific Otx2 enhancer element active in immature developing photoreceptors. Dev Biol 360:241-55
Cherry, Timothy J; Wang, Sui; Bormuth, Ingo et al. (2011) NeuroD factors regulate cell fate and neurite stratification in the developing retina. J Neurosci 31:7365-79
Bienvenu, Frédéric; Jirawatnotai, Siwanon; Elias, Joshua E et al. (2010) Transcriptional role of cyclin D1 in development revealed by a genetic-proteomic screen. Nature 463:374-8
Jadhav, Ashutosh P; Roesch, Karin; Cepko, Constance L (2009) Development and neurogenic potential of Muller glial cells in the vertebrate retina. Prog Retin Eye Res 28:249-62
Damiani, Devid; Alexander, John J; O'Rourke, Jason R et al. (2008) Dicer inactivation leads to progressive functional and structural degeneration of the mouse retina. J Neurosci 28:4878-87
Morrow, Eric M; Chen, C-M Amy; Cepko, Constance L (2008) Temporal order of bipolar cell genesis in the neural retina. Neural Dev 3:2
Kim, Douglas S; Ross, Sarah E; Trimarchi, Jeffrey M et al. (2008) Identification of molecular markers of bipolar cells in the murine retina. J Comp Neurol 507:1795-810

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