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Abstract #80857 Published in IGR 20-3
Mapping mRNA Expression of Glaucoma Genes in the Healthy Mouse Eye
Hubens WHG; Breddels EM; Walid Y; Ramdas WD; Webers CAB; Gorgels TGMF; Gorgels TGMFCurrent Eye Research 2019; 44: 1006-1017
Many genes have been associated with primary open-angle glaucoma (POAG). Knowing exactly where they are expressed in the eye helps to unravel POAG pathology and to select optimal targets for intervention. We investigated whether RNA hybridization (RNA-ISH) is a convenient technique to obtain detailed pan-ocular expression data of these genes. We tested this for four diverse candidate POAG genes, selected because of unclear ocular distribution ( and and relevance for potential new therapies (). , a POAG gene with well-known ocular expression pattern served as control. We made a list of candidate glaucoma genes reported in genetic studies. A table of their ocular expression at the tissue level was compiled using publicly available microarray data (the ocular tissue database). To add cellular detail we performed RNA-ISH for , and on eyes of healthy, 2-month-old, pigmented, and albino mice. Expression of the control matched with published immunohistochemistry data. Ocular expression of was generally low, with patches of higher expression, superficially in the corneal epithelium. had a restricted expression pattern with high expression in the nonpigmented ciliary body epithelium and moderate expression in the peripapillary region. and showed ubiquitous expression. RNA-ISH is a suitable technique to determine the ocular expression pattern of POAG genes, adding meaningful cellular detail to existing microarray expression data. For instance, the high expression of in the nonpigmented ciliary body epithelium suggests a role of this gene in aqueous humor dynamics and intraocular pressure. In addition, the ubiquitous expression of has implications for designing TGF-β-related glaucoma therapies, with respect to side effects. Creating pan-ocular expression maps of POAG genes with RNA-ISH will help to identify POAG pathways in specific cell types and to select targets for drug development.
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Classification:
3.5 Molecular biology incl. SiRNA (Part of: 3 Laboratory methods)
3.4.2 Gene studies (Part of: 3 Laboratory methods > 3.4 Molecular genetics)