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Targeted Editing of Myostatin Gene in Sheep by Transcription Activator-like Effector Nucleases

机译:转录激活因子样效应物核酸酶靶向编辑绵羊肌生长抑制素基因。

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摘要

Myostatin (MSTN) is a secreted growth factor expressed in skeletal muscle and adipose tissue that negatively regulates skeletal muscle mass. Gene knockout of MSTN can result in increasing muscle mass in sheep. The objectives were to investigate whether myostatin gene can be edited in sheep by transcription activator-like effector nucleases (TALENs) in tandem with single-stranded DNA oligonucleotides (ssODNs). We designed a pair of TALENs to target a highly conserved sequence in the coding region of the sheep MSTN gene. The activity of the TALENs was verified by using luciferase single-strand annealing reporter assay in HEK 293T cell line. Co-transfection of TALENs and ssODNs oligonucleotides induced precise gene editing of myostatin gene in sheep primary fibroblasts. MSTN gene-edited cells were successfully used as nuclear donors for generating cloned embryos. TALENs combined with ssDNA oligonucleotides provide a useful approach for precise gene modification in livestock animals.
机译:肌生长抑制素(MSTN)是在骨骼肌和脂肪组织中表达的一种分泌性生长因子,对骨骼肌质量产生负调节作用。 MSTN基因敲除可导致绵羊肌肉增加。目的是研究是否可以通过单链DNA寡核苷酸(ssODN)串联的转录激活因子效应子核酸酶(TALENs)在绵羊中编辑肌生长抑制素基因。我们设计了一对TALEN,以靶向绵羊MSTN基因编码区中的高度保守序列。通过使用荧光素酶单链退火报告基因测定法在HEK 293T细胞系中验证了TALENs的活性。 TALENs和ssODNs寡核苷酸的共转染可在绵羊原代成纤维细胞中诱导myostatin基因的精确基因编辑。 MSTN基因编辑的细胞已成功地用作产生克隆胚胎的核供体。 TALENs与ssDNA寡核苷酸结合提供了一种在牲畜中进行精确基因修饰的有用方法。

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