4.8 Article

Rapid and Integrative Discovery of Retina Regulatory Molecules

期刊

CELL REPORTS
卷 24, 期 9, 页码 2506-2519

出版社

CELL PRESS
DOI: 10.1016/j.celrep.2018.07.090

关键词

-

资金

  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]

向作者/读者索取更多资源

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.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据