Creation of an albino squid line by CRISPR-Cas9 and its application for in vivo functional imaging of neural activity

清脆的 生物 Cas9 基因组编辑 基因 核糖核蛋白 遗传学 头足类 伪装 八达通(软件) 突变 基因敲除 计算生物学 细胞生物学 突变 核糖核酸 物理 量子力学 动物 生态学
作者
Namrata Ahuja,Ernie Hwaun,Judit R. Pungor,Ruhina Rafiq,Sal Nemes,Taylor Sakmar,Miranda A. Vogt,Bret Grasse,Juan Diaz Quiroz,Tessa G. Montague,Ryan W. Null,Danielle N. Dallis,Daria Gavriouchkina,Ferdinand Marlétaz,Lisa Abbo,Daniel S. Rokhsar,Cristopher M. Niell,Iván Soltész,Caroline B. Albertin,Joshua J. C. Rosenthal
出处
期刊:Current Biology [Elsevier]
卷期号:33 (13): 2774-2783.e5 被引量:16
标识
DOI:10.1016/j.cub.2023.05.066
摘要

•Genetic lines of Euprymna berryi can be produced with CRISPR •The knockout of two pigmentation genes is required to produce albinos •Neural activity can be imaged non-invasively in the brains of albino lines Cephalopods are remarkable among invertebrates for their cognitive abilities, adaptive camouflage, novel structures, and propensity for recoding proteins through RNA editing. Due to the lack of genetically tractable cephalopod models, however, the mechanisms underlying these innovations are poorly understood. Genome editing tools such as CRISPR-Cas9 allow targeted mutations in diverse species to better link genes and function. One emerging cephalopod model, Euprymna berryi, produces large numbers of embryos that can be easily cultured throughout their life cycle and has a sequenced genome. As proof of principle, we used CRISPR-Cas9 in E. berryi to target the gene for tryptophan 2,3 dioxygenase (TDO), an enzyme required for the formation of ommochromes, the pigments present in the eyes and chromatophores of cephalopods. CRISPR-Cas9 ribonucleoproteins targeting tdo were injected into early embryos and then cultured to adulthood. Unexpectedly, the injected specimens were pigmented, despite verification of indels at the targeted sites by sequencing in injected animals (G0s). A homozygote knockout line for TDO, bred through multiple generations, was also pigmented. Surprisingly, a gene encoding indoleamine 2,3, dioxygenase (IDO), an enzyme that catalyzes the same reaction as TDO in vertebrates, was also present in E. berryi. Double knockouts of both tdo and ido with CRISPR-Cas9 produced an albino phenotype. We demonstrate the utility of these albinos for in vivo imaging of Ca2+ signaling in the brain using two-photon microscopy. These data show the feasibility of making gene knockout cephalopod lines that can be used for live imaging of neural activity in these behaviorally sophisticated organisms. Cephalopods are remarkable among invertebrates for their cognitive abilities, adaptive camouflage, novel structures, and propensity for recoding proteins through RNA editing. Due to the lack of genetically tractable cephalopod models, however, the mechanisms underlying these innovations are poorly understood. Genome editing tools such as CRISPR-Cas9 allow targeted mutations in diverse species to better link genes and function. One emerging cephalopod model, Euprymna berryi, produces large numbers of embryos that can be easily cultured throughout their life cycle and has a sequenced genome. As proof of principle, we used CRISPR-Cas9 in E. berryi to target the gene for tryptophan 2,3 dioxygenase (TDO), an enzyme required for the formation of ommochromes, the pigments present in the eyes and chromatophores of cephalopods. CRISPR-Cas9 ribonucleoproteins targeting tdo were injected into early embryos and then cultured to adulthood. Unexpectedly, the injected specimens were pigmented, despite verification of indels at the targeted sites by sequencing in injected animals (G0s). A homozygote knockout line for TDO, bred through multiple generations, was also pigmented. Surprisingly, a gene encoding indoleamine 2,3, dioxygenase (IDO), an enzyme that catalyzes the same reaction as TDO in vertebrates, was also present in E. berryi. Double knockouts of both tdo and ido with CRISPR-Cas9 produced an albino phenotype. We demonstrate the utility of these albinos for in vivo imaging of Ca2+ signaling in the brain using two-photon microscopy. These data show the feasibility of making gene knockout cephalopod lines that can be used for live imaging of neural activity in these behaviorally sophisticated organisms. Functional organization of visual responses in the octopus optic lobePungor et al.Current BiologyJune 20, 2023In BriefPungor et al. use calcium imaging to measure visually evoked response properties in the cephalopod central nervous system. They demonstrate shared and novel aspects of visual function in the octopus, including retinotopic organization, the emergence of ON and OFF pathways, and asymmetries in the processing of light and dark stimuli. Full-Text PDF Open AccessA brain atlas for the camouflaging dwarf cuttlefish, Sepia bandensisMontague et al.Current BiologyJune 20, 2023In BriefCephalopods are masters of dynamic camouflage and complex social behaviors, and they exhibit learning and memory. Montague et al. generate a brain atlas for a promising model cephalopod species, the dwarf cuttlefish, using magnetic resonance imaging, deep learning, and histology. They host the data on a custom-built interactive website, Cuttlebase. Full-Text PDF Open Access
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