Identification of Two Potential Gene Insertion Sites for Gene Editing on the Chicken Z/W Chromosomes

Author:

Wu Gaoyuan123ORCID,Liang Youchen123,Chen Chen123,Chen Guohong123,Zuo Qisheng123,Niu Yingjie1234,Song Jiuzhou5ORCID,Han Wei6,Jin Kai1234ORCID,Li Bichun1237ORCID

Affiliation:

1. Joint International Research Laboratory of Agriculture and Agri-Product Safety of Ministry of Education of China, Yangzhou University, Yangzhou 225009, China

2. Key Laboratory of Animal Breeding Reproduction and Molecular Design for Jiangsu Province, College of Animal Science and Technology, Yangzhou University, Yangzhou 225009, China

3. Institutes of Agricultural Science and Technology Development, Yangzhou University, Yangzhou 225009, China

4. College of Bioscience and Biotechnology, Yangzhou University, Yangzhou 225009, China

5. Department of Animal & Avian Sciences, University of Maryland, College Park, MD 20742, USA

6. Poultry Institute of Chinese Academy of Agricultural Sciences, Yangzhou 225003, China

7. College of Biotechnology, Jiangsu University of Science and Technology, Zhenjiang 212100, China

Abstract

The identification of accurate gene insertion sites on chicken sex chromosomes is crucial for advancing sex control breeding materials. In this study, the intergenic region NC_006127.4 on the chicken Z chromosome and the non-repetitive sequence EE0.6 on the W chromosome were selected as potential gene insertion sites. Gene knockout vectors targeting these sites were constructed and transfected into DF-1 cells. T7E1 enzyme cleavage and luciferase reporter enzyme analyses revealed knockout efficiencies of 80.00% (16/20), 75.00% (15/20), and 75.00% (15/20) for the three sgRNAs targeting the EE0.6 site. For the three sgRNAs targeting the NC_006127.4 site, knockout efficiencies were 70.00% (14/20), 60.00% (12/20), and 45.00% (9/20). Gel electrophoresis and high-throughput sequencing were performed to detect potential off-target effects, showing no significant off-target effects for the knockout vectors at the two sites. EdU and CCK-8 proliferation assays revealed no significant difference in cell proliferation activity between the knockout and control groups. These results demonstrate that the EE0.6 and NC_006127.4 sites can serve as gene insertion sites on chicken sex chromosomes for gene editing without affecting normal cell proliferation.

Funder

“JBGS” Project of Seed Industry Revitalization in Jiangsu Province

National Natural Science Foundation of China

China Postdoctoral Science Foundation

Publisher

MDPI AG

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