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• W2073818097 abstract "purpose. To identify in vivo a promoter fragment that specifically directs transgene expression in all zebrafish cone photoreceptors. This promoter subsequently enables GFP labeling of cones for facile morphologic analysis and purification and genetic rescue of achromatopsia. methods. Promoter fragments of the zebrafish cone transducin α (TαC) gene were subcloned upstream of EGFP and microinjected into one- to two-cell–stage embryos. Promoter activity was assessed by fluorescence microscopy in wholemounts and retinal cryosections, and cone photoreceptors were purified by flow cytometry. Visual physiology was assessed by the optokinetic response (OKR) assay. results. A 3.2-kb promoter fragment from zebrafish TαC specifically directed robust transgene expression in retinal cone photoreceptors and pineal photoreceptors. With this promoter, a stable transgenic line expressing EGFP in all zebrafish cone photoreceptors types was generated, and populations of cones were purified. Achromatopsia in the nof mutant was rescued using the identified promoter fragment to direct transgenic expression of wild-type cone transducin in mutant cones. conclusions. A 3.2-kb TαC promoter fragment replicates the temporal and spatial pattern of endogenous TαC expression. The integrity of cones can be readily assessed in an EGFP transgenic line generated with this promoter, enabling downstream genetic and chemical screens for cone determinants." @default.
• W2073818097 created "2016-06-24" @default.
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• W2073818097 date "2007-02-01" @default.
• W2073818097 modified "2023-09-23" @default.
• W2073818097 title "Identification of a Zebrafish Cone Photoreceptor–Specific Promoter and Genetic Rescue of Achromatopsia in the<i>nof</i>Mutant" @default.
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• W2073818097 doi "https://doi.org/10.1167/iovs.06-0975" @default.
• W2073818097 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/17251445" @default.
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