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The CRISPR/Cas9 induces large genomic fragment deletions of MSTN and phenotypic changes in sheep
DING Yi, ZHOU Shi-wei, DING Qiang, CAI Bei, ZHAO Xiao-e, ZHONG Shu, JIN Miao-han, WANG Xiao-long, MA Bao-hua, CHEN Yu-lin
2020, 19 (4): 1065-1073.   DOI: 10.1016/S2095-3119(19)62853-4
Abstract230)      PDF in ScienceDirect      
The CRISPR/Cas9 system has been extensively used to engineer genetic loci for the generation of knockouts, insertions, and point mutations in animal models.  However, many mutations that have been reported in animals are small insertions or deletions.  This study used the CRISPR/Cas9 system to induce large DNA fragment deletions in MSTN via three guide RNAs in sheep.  This successfully achieved the precise gene editing of the ovine MSTN gene by injecting both Cas9 mRNA and sgRNAs into embryos at the one-cell stage.  Of 10 edited animals, 3 animals (30%) exhibited large genomic fragment deletions (~5 kb).  Furthermore, the body weights of these 3 animals were significantly different (P0<0.0001, P15=0.001, P30=0.005, P60=0.027) between lambs with large deletions and wildtype lambs.  In addition, the edited lambs were also significantly different (P0<0.0001, P15<0.0001, P30=0.002, P60=0.011) compared with wildtype.  These results suggest that the generated MSTN knockout sheep is a reliable and effective animal model for further study.  Furthermore, this method is time- and labor-saving, and efficient for the creation of animal models for agriculture, biology, and medicine.
 
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Sheep with Partial RXFP2 Knockout Exhibit Normal Horn Phenotype but Unilateral Cryptorchidism
GAO Yawei, XI Siyuan, CAI Bei, WU Tingjie, WANG Qian, Peter KALDS, HUANG Shuhong, WANG Yuhui, HAN Saizheng, PAN Menghao, YANG Chong, KOU Qifang, MA Baohua, WANG Xiaolong, ZHOU Shiwei and CHEN Yulin
DOI: 10.1016/j.jia.2023.11.045 Online: 29 November 2023
Abstract68)      PDF in ScienceDirect      

Comprehending the genetic basis of economically important traits is of significant importance to enhance livestock breeding. In domestic ruminants, hornlessness is becoming a more desirable trait since horns could lead to accidental injuries to animals and producers. Recent studies have identified the relaxin family peptide receptor 2 (RXFP2) as a primary candidate gene associated with the presence and absence of horns in sheep. However, no sufficient molecular biology-based analyses were performed to validate the association and function of RXFP2 in sheep. Noticeably, previous studies in both humans and mice have provided evidence supporting the involvement of RXFP2 in testicular descent. To validate the potential function of the RXFP2 gene in sheep, we used the CRISPR/Cas9 technology to obtain RXFP2-disrupted sheep individuals. Initially, highly efficient sgRNAs, targeting RXFP2, were screening through in vitro cleavage assays and cellular assessments. Then, two RXFP2-disrupted lambs were generated by intracytoplasmic microinjection of CRISPR/Cas9-sg1 ribonucleoprotein, with an efficiency of 81.84 and 37.17%, respectively. No potential off-target events were detected. Western blot analysis showed that RXFP2 expression was significantly reduced in the pedicle skin of edited lambs (P=0.034). Intriguingly, although the partial disruption of RXFP2 did not affect the horn phenotype in sheep, it led to an obvious unilateral cryptorchidism. These results provide evidence for a hitherto ambiguous link between both horn and testicular development. In conclusion, this study represents the first successful generation of cryptorchid sheep models via the disruption of RXFP2 using CRISPR/Cas9. These findings provide new insights into the roles of RXFP2, whose partial disruption is associated with testicular descent rather than horn formation.

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