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Generation of tryptophan hydroxylase 2 gene knockout pigs by CRISPR/Cas9-mediated gene targeting

机译:通过CRISPR / Cas9介导的基因靶向产生色氨酸羟化酶2基因敲除猪

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摘要

Unbalanced brain serotonin (5-HT) levels have implications in various behavioral abnormalities and neuropsychiatric disorders. The biosynthesis of neuronal 5-HT is regulated by the rate-limiting enzyme, tryptophan hydroxylase-2 (TPH2). In the present study, the clustered regularly interspaced short palindromic repeat (CRISPR)/CRISPR-associated (Cas) system was used to target theTph2 gene in Bama mini pig fetal fibroblasts. It was found that CRISPR/Cas9 targeting efficiency could be as high as 61.5%, and the biallelic mutation efficiency reached at 38.5%. The biallelic modified colonies were used as donors for somatic cell nuclear transfer (SCNT) and 10Tph2 targeted piglets were successfully generated. These Tph2 KO piglets were viable and appeared normal at the birth. However, their central 5-HT levels were dramatically reduced, and their survival and growth rates were impaired before weaning. TheseTph2 KO pigs are valuable large-animal models for studies of 5-HT deficiency induced behavior abnomality.
机译:脑5-羟色胺(5-HT)水平的不平衡对各种行为异常和神经精神疾病具有影响。神经元5-HT的生物合成受限速酶色氨酸羟化酶2(TPH2)调控。在本研究中,聚类的规则间隔的短回文重复(CRISPR)/ CRISPR相关(Cas)系统用于靶向巴马迷你猪胎儿成纤维细胞中的Tph2基因。发现CRISPR / Cas9靶向效率可高达61.5%,双等位基因突变效率达到38.5%。双等位基因修饰的菌落用作体细胞核移植(SCNT)的供体,并成功产生了以10Tph2为目标的仔猪。这些Tph2 KO仔猪是有活力的,并且在出生时看起来很正常。但是,它们的中枢5-HT水平显着降低,断奶前它们的生存和生长速度受到损害。这些Tph2 KO猪是用于研究5-HT缺乏引起的行为异常的有价值的大型动物模型。

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