Hu Wenping, Dong Xinlong, Tian Zhilong, Zhang Zhuangbiao, Tang Jishun, Liang Benmeng, Liu Qiuyue, Chu Mingxing
Key Laboratory of Animal Genetics and Breeding and Reproduction of Ministry of Agriculture and Rural Affairs, Institute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing, 100193, China.
Institute of Animal Husbandry and Veterinary Medicine, Anhui Academy of Agricultural Sciences, Hefei, 230031, China.
J Anim Sci Biotechnol. 2021 Mar 12;12(1):37. doi: 10.1186/s40104-021-00548-4.
JUNO and IZUMO1 are the first receptor-ligand protein pairs discovered to be essential for sperm-oocyte fusion; their interaction is indispensable for fertilization.
PCR was used to clone the full-length DNA sequence of the Juno gene in sheep. The single nucleotide polymorphism (SNP) loci of Juno were genotyped by Sequenom MassARRAY®. PCR combined with rapid amplification of cDNA Ends were used to clone the full-length cDNA sequence of Juno and Izumo1. Reverse transcriptase-PCR (RT-PCR) and real time-quantitative-PCR (RT-qPCR) were used to analyze the genes' expression in tissues of sheep, and single cell RNA-seq was used to analyze the genes' expression in oocytes, granulosa cells and follicular theca of polytocous and monotocous Small Tail Han ewes. Bioinformatics was used to analyze advanced structure and phylogeny of JUNO and IZUMO1 proteins.
The full-length DNA sequence of the Juno gene in sheep was cloned and nine SNPs were screened. We found a significant association between the g.848253 C > A locus of Juno and litter size of Small Tail Han sheep (P < 0.05). The full-length cDNA sequence of Juno and Izumo1 genes from Small Tail Han sheep were obtained. We found a new segment of the Izumo1 CDS consisting of 35 bp, and we confirmed the Izumo1 gene has 9 exons, not 8. RT-qPCR showed that Juno and Izumo1 genes were highly expressed in ovarian and testicular tissues, respectively (P < 0.01). Single cell RNA-seq showed Juno was specifically expressed in oocytes, but not in granulosa cells or follicular theca, while Izumo1 displayed little to no expression in all three cell types. There was no difference in expression of the Juno gene in oocyte and ovarian tissue in sheep with different litter sizes, indicating expression of Juno is not related to litter size traits. Bioinformatic analysis revealed the g.848253 C > A locus of Juno results in a nonconservative missense point mutation leading to a change from Phe to Leu at position 219 in the amino acid sequence.
For the first time, this study systematically analyzed the expression, structure and function of Juno and Izumo1 genes and their encoded proteins in Small Tail Han sheep, providing the basis for future studies of the regulatory mechanisms of Juno and Izumo1 genes.
JUNO和IZUMO1是首次发现的对精卵融合至关重要的受体-配体蛋白对;它们的相互作用对受精不可或缺。
采用PCR技术克隆绵羊Juno基因的全长DNA序列。利用Sequenom MassARRAY®对Juno的单核苷酸多态性(SNP)位点进行基因分型。采用PCR结合cDNA末端快速扩增技术克隆Juno和Izumo1的全长cDNA序列。运用逆转录PCR(RT-PCR)和实时定量PCR(RT-qPCR)分析基因在绵羊组织中的表达情况,并通过单细胞RNA测序分析基因在多胎和单胎小尾寒羊的卵母细胞、颗粒细胞和卵泡膜细胞中的表达。利用生物信息学分析JUNO和IZUMO1蛋白的高级结构和系统发育。
克隆了绵羊Juno基因的全长DNA序列,筛选出9个SNP。我们发现Juno基因的g.848253 C>A位点与小尾寒羊的产羔数显著相关(P<0.05)。获得了小尾寒羊Juno和Izumo1基因的全长cDNA序列。我们发现Izumo1 CDS有一个由35 bp组成的新片段,并证实Izumo1基因有9个外显子,而非8个。RT-qPCR结果显示,Juno和Izumo1基因分别在卵巢和睾丸组织中高表达(P<0.01)。单细胞RNA测序表明,Juno特异性表达于卵母细胞,而在颗粒细胞或卵泡膜细胞中不表达,而Izumo1在这三种细胞类型中几乎不表达。不同产羔数绵羊的卵母细胞和卵巢组织中Juno基因的表达无差异,表明Juno的表达与产羔数性状无关。生物信息学分析显示,Juno基因的g.848253 C>A位点导致非保守错义点突变,使氨基酸序列第219位的苯丙氨酸变为亮氨酸。
本研究首次系统分析了小尾寒羊中Juno和Izumo1基因及其编码蛋白的表达、结构和功能,为今后研究Juno和Izumo1基因的调控机制提供了依据。