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Disruption of T-box transcription factor eomesa results in abnormal development of median fins in Oujiang color common carp Cyprinus carpio

文献类型： 外文期刊

作者： Song, Shiying 1 ; Du, Bobo 1 ; Chung-Davidson, Yu-Wen 3 ; Cui, Wenyao 1 ; Li, Yaru 1 ; Chen, Honglin 1 ; Huang, Rong 4 ; Li, Weiming 3 ; Li, Fei 5 ; Wang, Chenghui 1 ; Ren, Jianfeng 1 ;

作者机构： 1.Shanghai Ocean Univ, Key Lab Freshwater Aquat Genet Resources Certifica, Shanghai, Peoples R China

2.Guizhou Acad Agr Sci, Guizhou Inst Biotechnol, Guizhou Key Lab Agr Biotechnol, Guiyang, Peoples R China

3.Michigan State Univ, Dept Fisheries & Wildlife, E Lansing, MI USA

4.Guangdong Aquarium Assoc, Guangzhou, Peoples R China

5.Zhejiang Inst Freshwater Fisheries, Key Lab Freshwater Aquaculture Genet & Breeding Zh, Huzhou, Peoples R China

期刊名称：PLOS ONE （ 影响因子：3.7； 五年影响因子：3.8 ）

ISSN： 1932-6203

年卷期： 2023 年 18 卷 3 期

页码：

收录情况： SCI

摘要： Median fins are thought to be ancestors of paired fins which in turn give rise to limbs in tetrapods. However, the developmental mechanisms of median fins remain largely unknown. Nonsense mutation of the T-box transcription factor eomesa in zebrafish results in a phenotype without dorsal fin. Compared to zebrafish, the common carp undergo an additional round of whole genome duplication, acquiring an extra copy of protein-coding genes. To verify the function of eomesa genes in common carp, we established a biallelic gene editing technology in this tetraploidy fish through simultaneous disruption of two homologous genes, eomesa1 and eomesa2. We targeted four sites located upstream or within the sequences encoding the T-box domain. Sanger sequencing data indicated the average knockout efficiency was around 40% at T1-T3 sites and 10% at T4 site in embryos at 24 hours post fertilization. The individual editing efficiency was high to about 80% at T1-T3 sites and low to 13.3% at T4 site in larvae at 7 days post fertilization. Among 145 mosaic F-0 examined at four months old, three individuals (Mutant 1-3) showed varying degrees of maldevelopment in the dorsal fin and loss of anal fin. Genotyping showed the genomes of all three mutants were disrupted at T3 sites. The null mutation rates on the eomesa1 and eomesa2 loci were 0% and 60% in Mutant 1, 66.7% and 100% in Mutant 2, and 90% and 77.8% in Mutant 3, respectively. In conclusion, we demonstrated a role of eomesa in the formation and development of median fins in Oujiang color common carp and established an method that simultaneously disrupt two homologous genes with one gRNA, which would be useful in genome editing in other polyploidy fishes.

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