Suppr超能文献

鉴定鸡 Z/W 染色体基因编辑的两个潜在基因插入位点。

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

机构信息

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

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

出版信息

Genes (Basel). 2024 Jul 22;15(7):962. doi: 10.3390/genes15070962.

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.

摘要

准确鉴定鸡性染色体上的基因插入位点对于推进性别控制育种材料至关重要。本研究选择鸡 Z 染色体上的基因间区 NC_006127.4 和 W 染色体上的非重复序列 EE0.6 作为潜在的基因插入位点。构建了针对这些位点的基因敲除载体,并转染至 DF-1 细胞中。T7E1 酶切和荧光素酶报告酶分析显示,针对 EE0.6 位点的三个 sgRNA 的敲除效率分别为 80.00%(16/20)、75.00%(15/20)和 75.00%(15/20)。针对 NC_006127.4 位点的三个 sgRNA 的敲除效率分别为 70.00%(14/20)、60.00%(12/20)和 45.00%(9/20)。凝胶电泳和高通量测序检测潜在的脱靶效应,结果显示两个位点的敲除载体均无明显的脱靶效应。EdU 和 CCK-8 增殖实验显示,敲除组和对照组细胞增殖活性无显著差异。这些结果表明,EE0.6 和 NC_006127.4 位点可作为鸡性染色体上的基因插入位点进行基因编辑,而不会影响正常细胞增殖。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c0c2/11276091/672f0f8c230f/genes-15-00962-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验