Temperature influences sex determination in the giant spiny frog (Quasipaa spinosa) via alteration of DNA methylation and transcriptional profiles

DNA甲基化 表观遗传学 转录组 生物 甲基化 基因 CpG站点 发起人 基因表达调控 基因表达 DNA 雌激素 遗传学 性别分化 细胞生物学 睾酮(贴片) 熔化温度 差异甲基化区 性激素结合球蛋白 后生 分子生物学 转录调控
作者
Piao Zhu,Peng Xu,Yibin Hu,Haochen Huang,Gang Wan,Yehong Lin,Xinhao Zhang,Han Li,Rongquan Zheng
出处
期刊:Aquaculture Reports [Elsevier BV]
卷期号:46: 103399-103399 被引量:1
标识
DOI:10.1016/j.aqrep.2026.103399
摘要

Temperature is a critical environmental factor influencing DNA epigenetic modifications. While the role of DNA methylation in gene regulation is well-established, its interplay with environmental signals in amphibians remains inadequately understood. In this study, Quasipaa spinosa tadpoles were reared at 18 ℃ (low), 23℃ (normal), and 28 ℃ (high). Sex ratios were recorded, and transcriptome and whole-genome methylation sequencing were performed. The normal-temperature group exhibited a balanced 1:1 sex ratio, while high temperature induced masculinization and low temperature promoted feminization. Although no significant differences in overall DNA methylation levels were observed, key pathways involved in sex-hormone synthesis were altered in a temperature-dependent manner. Specifically, low temperature activated CACN family genes and upregulated CYP19A1 , thereby enhancing estrogen synthesis and promoting female differentiation. In contrast, high temperature suppressed CYP19A1 activity, resulting in testosterone accumulation and masculinization. These results elucidate a pathway through which temperature influences sex determination in Q. spinosa via epigenetic regulation, providing a theoretical basis for the precise control of sex ratios in aquaculture. • Integrated methylome and transcriptome analyses reveal temperature effects on sex determination in Quasipaa spinosa tadpoles. • Low (18 ℃) feminized and high (28 ℃) masculinized tadpoles; the normal 23 ℃ group showed an approximately 1:1 sex ratio. • Temperature had minimal effects on global DNA methylation but altered key sex-related genes in a tissue-specific manner. • Revealed a negative link between promoter methylation and transcription, and a temperature-dependent sex hormone pathway.
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