College of Fisheries, Key Lab of Agricultural Animal Genetics, Breeding and Reproduction of Ministry of Education/Key Lab of Freshwater Animal Breeding, Ministry of Agriculture, Huazhong Agricultural University, Wuhan, 437000, Hubei, People's Republic of China.
Hubei Provincial Engineering Laboratory for Pond Aquaculture, No. 1 Shizishan Stress, Hongshan District, Wuhan, 430070, Hubei Province, People's Republic of China.
Transgenic Res. 2019 Aug;28(3-4):341-356. doi: 10.1007/s11248-019-00125-6. Epub 2019 Jun 10.
CRISPR/Cas9 system has been developed as a highly efficient genome editing technology to specifically induce mutations in a few aquaculture species. In this study, we described induction of targeted gene (namely tyrosinase, tyr) mutations in large-scale loach Paramisgurnus dabryanus, an important aquaculture fish species and a potential model organism for studies of intestinal air-breathing function, using the CRISPR/Cas9 system. Tyr gene in large-scale loach was firstly cloned and then its expressions were investigated. Two guide RNAs (gRNAs) were designed and separately transformed with Cas9 in the loach. 89.4% and 96.1% of injected loach juveniles respectively displayed a graded loss of pigmentation for the two gRNAs, in other words, for target 1 and target 2. We classified the injected loach juveniles into five groups according to their skin color phenotypes, including four albino groups and one wild-type-like group. And one of them was clear albino group, which was of high ornamental and commercial value. More than 50 clones for each albino transformant with a visible phenotype in each target were randomly selected and sequenced. Results obtained here showed that along with the increase of pigmentation, wild-type alleles appeared in the injected loach juveniles more often and insertion/deletion alleles less frequently. This study demonstrated that CRISPR/Cas9 system could be practically performed to modify large-scale loach tyr to produce an albino mutant of high ornamental and commercial value, and for the first time showed successful use of the CRISPR/Cas9 system for genome editing in a Cobitidae species.
CRISPR/Cas9 系统已被开发为一种高效的基因组编辑技术,可特异性地在几种水产养殖物种中诱导突变。在这项研究中,我们描述了使用 CRISPR/Cas9 系统在大规模泥鳅 Paramisgurnus dabryanus 中诱导靶向基因(即酪氨酸酶,tyr)突变。首先克隆了大规模泥鳅中的 tyr 基因,然后研究了其表达。设计了两个向导 RNA(gRNA),并分别将其与 Cas9 转化为泥鳅。两种 gRNA 分别使 89.4%和 96.1%的注射泥鳅幼鱼出现不同程度的色素沉着缺失,即靶向 1 和靶向 2。根据皮肤颜色表型,我们将注射的泥鳅幼鱼分为五组,包括四组白化组和一组野生型样组。其中一组是明显的白化组,具有很高的观赏和商业价值。对每个靶标中具有可见表型的每个白化转化体随机选择并测序超过 50 个克隆。结果表明,随着色素沉着的增加,野生型等位基因在注射的泥鳅幼鱼中出现的频率更高,插入/缺失等位基因出现的频率更低。这项研究表明,CRISPR/Cas9 系统可实际用于修饰大规模泥鳅 tyr,以产生具有高观赏和商业价值的白化突变体,这是首次成功将 CRISPR/Cas9 系统用于 Cobitidae 物种的基因组编辑。