Zhang Bochao, Zhu Genbao, Wu Jianling, Xie Huihui, Cui Jiankun, Qian Wei, Yi Qing, Pan Fuqiang, Fang Fugui, Ling Yinghui, Zhang Yunhai, Li Yunsheng, Liu Ya
College of Veterinary Medicine, Anhui Agricultural University, Hefei, Anhui, China.
AnhuiWanbei Electricity Group General Hospital, Suzhou, Anhui, China.
Sci Rep. 2025 Jan 17;15(1):2269. doi: 10.1038/s41598-024-84559-x.
Previous studies have confirmed that methylation regulates gene transcription in the hypothalamus-pituitary-gonadal axis during puberty initiation, but little is known about the regulation of DNA methylation on gene expression in the pineal gland. To screen pineal gland candidate genes related to the onset of goat puberty and regulated by genome methylation, we collected pineal glands from prepubertal and pubertal female goats, then, determined the DNA methylation profile by whole genome bisulfite sequencing and the transcriptome by RNA sequencing on Illumina HiSeqTM2500. We analyzed differentially expressed genes between the Pre group and Pub group using the DESeq2 software (version 1.20.0), and applied the Benjamini and Hochberg method for adjusting P-values. Genes with a P-value less than 0.05 and an absolute log2 fold change greater than 0 were considered differentially expressed genes. Results showed that there was no significant difference in the whole-genome methylation level of the pineal gland between prepubertal and pubertal goats, but the methylation pattern changed significantly, indicating that genomic DNA methylation of the pineal gland might play a role in regulating the initiation of goat puberty. Changes in DNA methylation patterns affected some pineal gland transcriptomes, while the transcriptional level of most genes remained unaffected by DNA methylation differences. Genes regulated by DNA methylation regulates genes primarily involved in metabolic processes, oxidative phosphorylation, and signaling pathways related to thermogenesis. Methylation significantly regulated the expression of genes such as ATP5F1D, CACNB2, and PTEN, while genes like LIN28B, GIP, OPN1SW, and DCC showed the most notable fold changes, which may indicate their involvement in the onset of puberty.
先前的研究已经证实,甲基化在青春期启动过程中调节下丘脑 - 垂体 - 性腺轴中的基因转录,但关于DNA甲基化对松果体中基因表达的调节作用知之甚少。为了筛选与山羊青春期启动相关且受基因组甲基化调控的松果体候选基因,我们收集了青春期前和青春期雌性山羊的松果体,然后通过全基因组亚硫酸氢盐测序确定DNA甲基化图谱,并在Illumina HiSeqTM2500上通过RNA测序确定转录组。我们使用DESeq2软件(版本1.20.0)分析了Pre组和Pub组之间的差异表达基因,并应用Benjamini和Hochberg方法调整P值。P值小于0.05且绝对log2倍数变化大于0的基因被视为差异表达基因。结果表明,青春期前和青春期山羊松果体的全基因组甲基化水平没有显著差异,但甲基化模式发生了显著变化,这表明松果体的基因组DNA甲基化可能在调节山羊青春期启动中发挥作用。DNA甲基化模式的变化影响了一些松果体转录组,而大多数基因的转录水平不受DNA甲基化差异的影响。受DNA甲基化调控的基因主要参与代谢过程、氧化磷酸化以及与产热相关的信号通路。甲基化显著调节了ATP5F1D、CACNB2和PTEN等基因的表达,而LIN28B、GIP、OPN1SW和DCC等基因的倍数变化最为显著,这可能表明它们参与了青春期的启动。