Abstract:
The anemonefish Amphiprion ocellarisis highly popular in the ornamental fish trade due to its distinctive coloration, which features a combination of orange, black, and white. The formation of black pigmentation in teleost fish is controlled by the tyrosinase-producing gene (tyr), which is responsible for melanin production. Studies have indicated that deletion mutations in the tyrgene family in fish and many other vertebrates lead to skin color abnormalities, such as albinism. The clustered regularly interspaced short palindromic repeat (CRISPR) system has emerged as a powerful and precise tool for gene editing with diverse applications. In this study, we construct a CRISPR/Cas9 system targeting the exon 2 region of the tyrgene in A. ocellaris. A guide RNA (gRNA) was designed and incorporated into the gRNA cloning vector and was subsequently introduced into Escherichia colistrain DH5-α. Afterward, the successfully incorporated gRNA sequence was validated via Sanger sequencing. The E. coliDH5-α strains carrying this recombinant plasmid were subsequently checked and screened for stability via generations. This gRNA vector together with the Cas9 plasmid will be used to generate knock-out mutations, enabling further investigation ofthe function of the tyrgene in melanin formation in anemonefish A. ocellaris.
