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利用定制内切酶实现家畜中非减数分裂等位基因的高效导入。

Efficient nonmeiotic allele introgression in livestock using custom endonucleases.

机构信息

Department of Animal Science, University of Minnesota, Saint Paul, MN 55108.

出版信息

Proc Natl Acad Sci U S A. 2013 Oct 8;110(41):16526-31. doi: 10.1073/pnas.1310478110. Epub 2013 Sep 6.

Abstract

We have expanded the livestock gene editing toolbox to include transcription activator-like (TAL) effector nuclease (TALEN)- and clustered regularly interspaced short palindromic repeats (CRISPR)/Cas9-stimulated homology-directed repair (HDR) using plasmid, rAAV, and oligonucleotide templates. Toward the genetic dehorning of dairy cattle, we introgressed a bovine POLLED allele into horned bull fibroblasts. Single nucleotide alterations or small indels were introduced into 14 additional genes in pig, goat, and cattle fibroblasts using TALEN mRNA and oligonucleotide transfection with efficiencies of 10-50% in populations. Several of the chosen edits mimic naturally occurring performance-enhancing or disease- resistance alleles, including alteration of single base pairs. Up to 70% of the fibroblast colonies propagated without selection harbored the intended edits, of which more than one-half were homozygous. Edited fibroblasts were used to generate pigs with knockout alleles in the DAZL and APC genes to model infertility and colon cancer. Our methods enable unprecedented meiosis-free intraspecific and interspecific introgression of select alleles in livestock for agricultural and biomedical applications.

摘要

我们已经扩展了家畜基因编辑工具包,包括转录激活因子样效应物核酸酶(TALEN)和簇状规律间隔短回文重复(CRISPR)/Cas9 刺激的同源定向修复(HDR),使用质粒、rAAV 和寡核苷酸模板。为了实现奶牛的基因去角,我们将牛的 POLLED 等位基因导入有角公牛成纤维细胞。使用 TALEN mRNA 和寡核苷酸转染,在猪、山羊和牛成纤维细胞中引入了 14 个额外基因的单核苷酸改变或小插入缺失,效率为 10-50%。选择的编辑中的几个模仿了自然发生的增强性能或抗疾病的等位基因,包括单个碱基对的改变。高达 70%的未经过选择的成纤维细胞克隆携带预期的编辑,其中一半以上是纯合的。编辑后的成纤维细胞用于生成 DAZL 和 APC 基因敲除等位基因的猪,以模拟不育和结肠癌。我们的方法为农业和生物医学应用提供了前所未有的选择等位基因的无减数分裂种内和种间导入。

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