Zhang Jin, Zhang Xiang-Qian, Ling Xuan-Ze, Zhao Xiu-Hua, Zhou Kai-Zhi, Wang Jin-Yu, Zhang Gen-Xi
College of Animal Science and Technology, Yangzhou University, Yangzhou 225000, China.
Institute of Animal Husbandry, Heilongjiang Academy of Agricultural Sciences, Harbin 150001, China.
Vet Sci. 2022 Oct 16;9(10):570. doi: 10.3390/vetsci9100570.
Egg production in chickens is a quantitative trait. The aim of this study was to investigate the effect of promoter methylation of the Zona pellucida 2 (ZP2) gene on egg production. Real-time fluorescence quantification showed that the expression of the ZP2 gene in the ovaries of 300-day-old Jinghai yellow chickens in the high-laying group was significantly higher than that in the low-laying group (p < 0.01). A series of deletion fragments of the ZP2 gene promoter in Jinghai yellow chickens had different promoter activities in DF-1 cells, and the core region of the ZP2 gene promoter was found to be between −1552 and −1348. Four CpG islands in the promoter region of the ZP2 gene were detected by software prediction. The overall degree of methylation of the ZP2-1 amplified fragment was negatively correlated with mRNA expression to some extent (R = −0.197); the overall degree of methylation of the ZP2-2 amplified fragment was also negatively correlated with mRNA expression to some extent (R = −0.264), in which the methylation of methylcytosine (mC)-9, mC-20, and mC-21 sites was significantly negatively correlated with mRNA expression (p < 0.05). In addition, the mC-20 and mC-21 sites are located on the Sp1 transcription factor binding site, and it is speculated that these two sites may be the main sites for regulating transcription. In summary, the methylation sites mC-20 and mC-21 of the ZP2 gene may inhibit the binding of Sp1 and DNA, affect the transcription of the ZP2 gene, and then affect the number of eggs produced by the Jinghai yellow chickens.
鸡的产蛋量是一个数量性状。本研究旨在探讨透明带2(ZP2)基因启动子甲基化对产蛋量的影响。实时荧光定量显示,高产蛋组300日龄京海黄鸡卵巢中ZP2基因的表达显著高于低产蛋组(p < 0.01)。京海黄鸡ZP2基因启动子的一系列缺失片段在DF-1细胞中具有不同的启动子活性,发现ZP2基因启动子的核心区域在−1552至−1348之间。通过软件预测检测到ZP2基因启动子区域的四个CpG岛。ZP2-1扩增片段的总体甲基化程度与mRNA表达在一定程度上呈负相关(R = −0.197);ZP2-2扩增片段的总体甲基化程度也与mRNA表达在一定程度上呈负相关(R = −0.264),其中甲基胞嘧啶(mC)-9、mC-20和mC-21位点的甲基化与mRNA表达显著负相关(p < 0.05)。此外,mC-20和mC-21位点位于Sp1转录因子结合位点上,推测这两个位点可能是调节转录的主要位点。综上所述,ZP2基因的甲基化位点mC-20和mC-21可能抑制Sp1与DNA的结合,影响ZP2基因的转录,进而影响京海黄鸡的产蛋数。