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| Funder | NATIONAL EYE INSTITUTE |
|---|---|
| Recipient Organization | University of Pittsburgh At Pittsburgh |
| Country | United States |
| Start Date | Sep 01, 2024 |
| End Date | Mar 31, 2029 |
| Duration | 1,672 days |
| Number of Grantees | 1 |
| Roles | Principal Investigator |
| Data Source | NIH (US) |
| Grant ID | 10980097 |
SUMMARY: The proper execution of transcriptional programs in retinal progenitor cells is extremely critical for retinal formation as dysregulation of this process leads to severely compromised retinogenesis and the development of ocular disorders, including anophthalmia or microphthalmia. The wiring and rewiring of chromatin landscape constitutes an essential
mechanism to precise spatial and temporal regulation of gene expression during retinal differentiation, yet our understanding to this process remains inadequate. Our goal is to utilize state-of-the-art genomic technologies to provide a deep understanding to the genetic and epigenetic circuits that underlie retinal transcription programs and how perturbations in the retinal
core regulatory networks lead to congenital syndromes. In the first aim of this proposal, we will use mouse models to dissect the molecular, cellular, and genomic effects of genetic mutations on retinal development. In aim 2, we will elucidate how the chromatin landscape is wired by transcription factors in retinal progenitor cells. In aim 3, we will explore how coordination among
components of the core regulatory network drive retinogenesis epigenetically and transcriptionally. When completed, the results of this proposal will bridge a gap in our understanding to the chromatin-based regulatory mechanism underlying retinal genesis, a necessary knowledge to enhance strategies to diagnose, treat or prevent the devastating
consequences of congenital vision deficiency.
University of Pittsburgh At Pittsburgh
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