Key Laboratory of Animal Genetics, Breeding and Reproduction, Ministry of Agriculture and Rural Affairs, Institute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing 100193, China.
Int J Mol Sci. 2022 Oct 11;23(20):12060. doi: 10.3390/ijms232012060.
The Polled Celtic (Pc) mutation locus is a genetically simple single mutation that is the best choice for breeding polled cattle using gene editing. However, the mechanism of the Pc locus for regulating horn development is unclear, so we used gene editing, somatic cell nuclear transfer and embryo transfer to obtain polled Holstein fetal bovine (gestation time 90 days) with a homozygous Pc insertion (gene-edited Holstein fetal bovine, EH) and the wild-type 90 days Holstein fetal bovine (WH) as controls. The hematoxylin-eosin (HE) staining results showed that, compared to the WH, the EH horn buds had no white keratinized projections or vacuolated keratinocytes and no thick nerve bundles under the dermal tissue. Furthermore, DNA sequencing results showed that the Pc locus was homozygously inserted into the fetal bovine genome. A total of 791 differentially expressed genes were identified by transcriptome sequencing analysis. Enrichment analysis and protein interaction analysis results of differentially expressed genes showed that abundant gene changes after Pc insertion were associated with the adhesion molecule regulation, actin expression, cytoskeletal deformation and keratin expression and keratinization. It was also noted that the results contained several genes that had been reported to be associated with the development of horn traits, such as and . This study identified these changes for the first time and summarized them. The results suggested that the Pc mutant locus may inhibit neural crest cell EMT generation and keratin expression, leading to failures in neural crest cell migration and keratinization of the horn bud tissue, regulating the production of the polled phenotype.
无角陶赛特(Pc)突变基因座是一个遗传结构简单的单一突变,是利用基因编辑培育无角牛的最佳选择。然而,Pc 基因座调节角发育的机制尚不清楚,因此我们使用基因编辑、体细胞核移植和胚胎移植技术,获得了 Pc 插入纯合子的无角荷斯坦胎儿牛(妊娠期 90 天;基因编辑荷斯坦胎儿牛,EH)和野生型 90 天荷斯坦胎儿牛(WH)作为对照。苏木精-伊红(HE)染色结果表明,与 WH 相比,EH 角芽没有白色角蛋白化突起或空泡化角蛋白细胞,真皮组织下也没有厚的神经束。此外,DNA 测序结果表明,Pc 基因座被纯合插入了胎牛基因组中。通过转录组测序分析,共鉴定出 791 个差异表达基因。差异表达基因的富集分析和蛋白质相互作用分析结果表明,Pc 插入后大量基因变化与黏附分子调控、肌动蛋白表达、细胞骨架变形和角蛋白表达及角化有关。还注意到,结果中包含了几个先前报道与角性状发育相关的基因,如 和 。本研究首次发现并总结了这些变化。结果表明,Pc 突变基因座可能抑制神经嵴细胞 EMT 的发生和角蛋白的表达,导致神经嵴细胞迁移失败和角芽组织的角蛋白化失败,从而调节无角表型的产生。