Suppr超能文献

利用CRISPR/Cas9系统在兔中高效进行双sgRNA引导的大基因缺失

Efficient dual sgRNA-directed large gene deletion in rabbit with CRISPR/Cas9 system.

作者信息

Song Yuning, Yuan Lin, Wang Yong, Chen Mao, Deng Jichao, Lv Qingyan, Sui Tingting, Li Zhanjun, Lai Liangxue

机构信息

Jilin Provincial Key Laboratory of Animal Embryo Engineering, Jilin University, Changchun, 130062, China.

出版信息

Cell Mol Life Sci. 2016 Aug;73(15):2959-68. doi: 10.1007/s00018-016-2143-z. Epub 2016 Jan 27.

Abstract

The CRISPR RNA-guided Cas9 nuclease gene-targeting system has been extensively used to edit the genome of several organisms. However, most mutations reported to date have been are indels, resulting in multiple mutations and numerous alleles in targeted genes. In the present study, a large deletion of 105 kb in the TYR (tyrosinase) gene was generated in rabbit via a dual sgRNA-directed CRISPR/Cas9 system. The typical symptoms of albinism accompanied significantly decreased expression of TYR in the TYR knockout rabbits. Furthermore, the same genotype and albinism phenotype were found in the F1 generation, suggesting that large-fragment deletions can be efficiently transmitted to the germline and stably inherited in offspring. Taken together, our data demonstrate that mono and biallelic large deletions can be achieved using the dual sgRNA-directed CRISPR/Cas9 system. This system produces no mosaic mutations or off-target effects, making it an efficient tool for large-fragment deletions in rabbit and other organisms.

摘要

CRISPR RNA引导的Cas9核酸酶基因靶向系统已被广泛用于编辑多种生物的基因组。然而,迄今为止报道的大多数突变都是插入缺失,导致靶向基因中出现多个突变和众多等位基因。在本研究中,通过双sgRNA引导的CRISPR/Cas9系统在兔中产生了TYR(酪氨酸酶)基因105 kb的大片段缺失。白化病的典型症状伴随着TYR基因敲除兔中TYR表达的显著降低。此外,在F1代中发现了相同的基因型和白化病表型,这表明大片段缺失可以有效地传递到生殖系并在后代中稳定遗传。综上所述,我们的数据表明,使用双sgRNA引导的CRISPR/Cas9系统可以实现单等位基因和双等位基因的大片段缺失。该系统不会产生嵌合突变或脱靶效应,使其成为兔和其他生物中大片段缺失的有效工具。

相似文献

引用本文的文献

2
mutation leads to chronic pancreatitis in rabbits.突变会导致兔子患上慢性胰腺炎。
Zool Res. 2025 May 18;46(3):647-660. doi: 10.24272/j.issn.2095-8137.2024.419.

本文引用的文献

3
Generation of multi-gene knockout rabbits using the Cas9/gRNA system.利用Cas9/gRNA系统生成多基因敲除兔。
Cell Regen. 2014 Sep 27;3(1):12. doi: 10.1186/2045-9769-3-12. eCollection 2014.

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