The main objective of the Eye Mutant Resource (EMR) is to identify, characterize, and preserve mice with genetically caused ocular disorders. Our purpose is to distribute these well-characterized models quickly and efficiently to support and promote vision research with the ultimate goal of advancing the elucidation, treatment, and cure of heritable eye diseases. Award of this grant is critical to the continuation of this unique resource. In this application, we will work toward enhancing the present EMR by developing robust genotyping protocols, fixing the genetic backgrounds of mutants to allow for comparison across mutations, cryo-preserving mutants to ensure their future availability, and improving the accessibility of the information in our EMR database. We will also increase the number of ocular mutants available to the research community two-fold during the grant period and continue our very successful screening program for new mutants with ocular diseases. Finally, we will complete the initial phenotypic and/or molecular characterization of ocular mutants previously identified, focusing initially on eight models exhibiting sub-retinal neovascularization. The models themselves and the information gathered on each mutant will be available to the research community through literature, electronic publications, and the updated EMR web site. It is expected that with the concerted effort and contribution from many groups using the EMR models, cumulatively, we will make a very significant impact on vision research.
Models to study eye diseases that occur in humans are important as reproducible experimental systems for elucidating pathways of normal development and function. Further, these models can be used to identify treatment targets and to test therapeutic strategies. The EMR focuses on identifying, characterizing and distributing such models.
|Sluch, Valentin M; Banks, Angela; Li, Hui et al. (2018) ADIPOR1 is essential for vision and its RPE expression is lost in the Mfrprd6 mouse. Sci Rep 8:14339|
|Yao, Kai; Qiu, Suo; Wang, Yanbin V et al. (2018) Restoration of vision after de novo genesis of rod photoreceptors in mammalian retinas. Nature 560:484-488|
|Chang, Bo; FitzMaurice, Bernard; Wang, Jieping et al. (2018) Spontaneous Posterior Segment Vascular Disease Phenotype of a Mouse Model, rnv3, Is Dependent on the Crb1rd8 Allele. Invest Ophthalmol Vis Sci 59:5127-5139|
|Peachey, Neal S; Hasan, Nazarul; FitzMaurice, Bernard et al. (2017) A missense mutation in Grm6 reduces but does not eliminate mGluR6 expression or rod depolarizing bipolar cell function. J Neurophysiol 118:845-854|
|Zhang, Hua; Li, Xia; Dai, Xufeng et al. (2017) The Degeneration and Apoptosis Patterns of Cone Photoreceptors inrd11Mice. J Ophthalmol 2017:9721362|
|Ji, Xiaojie; Chang, Bo; Naggert, Jürgen K et al. (2016) Lysosomal Trafficking Regulator (LYST). Adv Exp Med Biol 854:745-50|
|Luna, Gabriel; Lewis, Geoffrey P; Linberg, Kenneth A et al. (2016) Anatomical and Gene Expression Changes in the Retinal Pigmented Epithelium Atrophy 1 (rpea1) Mouse: A Potential Model of Serous Retinal Detachment. Invest Ophthalmol Vis Sci 57:4641-54|
|Chang, Bo (2016) Mouse Models as Tools to Identify Genetic Pathways for Retinal Degeneration, as Exemplified by Leber's Congenital Amaurosis. Methods Mol Biol 1438:417-30|
|Johnson, Kenneth R; Gagnon, Leona H; Chang, Bo (2016) A hypomorphic mutation of the gamma-1 adaptin gene (Ap1g1) causes inner ear, retina, thyroid, and testes abnormalities in mice. Mamm Genome 27:200-12|
|Ji, Xiaojie; Liu, Ye; Hurd, Ron et al. (2016) Retinal Pigment Epithelium Atrophy 1 (rpea1): A New Mouse Model With Retinal Detachment Caused by a Disruption of Protein Kinase C, ?. Invest Ophthalmol Vis Sci 57:877-88|
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