4.8 Article

Rapid and Integrative Discovery of Retina Regulatory Molecules

Journal

CELL REPORTS
Volume 24, Issue 9, Pages 2506-2519

Publisher

CELL PRESS
DOI: 10.1016/j.celrep.2018.07.090

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Funding

  1. NIH [R00AG044444, DP2EY02798, 1S10 OD016167]
  2. Cancer Prevention Research Institute of Texas
  3. Brain Research Foundation
  4. NIH
  5. National Institute of General Medical Sciences [T32GM088129]
  6. Robert and Janice McNair Foundation McNair MD/PhD Student Scholar Program
  7. RNA In Situ Hybridization Core facility at BMC
  8. NIH (IDDRC) [1U54 HD083092]
  9. NIH (Eunice Kennedy Shriver National Institute of Child Health and Human Development)
  10. KOMP2 [UM1HG006348, U42OD11174, U54HG006348]

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Retinal function relies on precisely organized neurons and synapses and a properly patterned vasculature to support them. Alterations in these features can result in vision loss. However, our understanding of retinal organization pathways remains incomplete because of a lack of methods to rapidly identify neuron and vasculature regulators in mammals. Here we developed a pipeline for the identification of neural and synaptic integrity genes by high-throughput retinal screening (INSiGHT) that analyzes candidate expression, vascular patterning, cellular organization, and synaptic arrangement. Using this system, we examined 102 mutant mouse lines and identified 16 unique retinal regulatory genes. Fifteen of these candidates are identified as novel retina regulators, and many (9 of 16) are associated with human neural diseases. These results expand the genetic landscape involved in retinal circuit organization and provide a road map for continued discovery of mammalian retinal regulators and disease-causing alleles.

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