Imprinting at the KBTBD6 locus involves species-specific maternal methylation and monoallelic expression in livestock animals.

IF 6.3 Q1 AGRICULTURE, DAIRY & ANIMAL SCIENCE
Jinsoo Ahn, In-Sul Hwang, Mi-Ryung Park, Seongsoo Hwang, Kichoon Lee
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Abstract

Background: The primary differentially methylated regions (DMRs) which are maternally hypermethylated serve as imprinting control regions (ICRs) that drive monoallelic gene expression, and these ICRs have been investigated due to their implications in mammalian development. Although a subset of genes has been identified as imprinted, in-depth comparative approach needs to be developed for identification of species-specific imprinted genes. Here, we examined DNA methylation status and allelic expression at the KBTBD6 locus across species and tissues and explored potential mechanisms of imprinting.

Results: Using whole-genome bisulfite sequencing and RNA-sequencing on parthenogenetic and normal porcine embryos, we identified a maternally hypermethylated DMR between the embryos at the KBTBD6 promoter CpG island and paternal monoallelic expression of KBTBD6. Also, in analyzed domesticated mammals but not in humans, non-human primates and mice, the KBTBD6 promoter CpG islands were methylated in oocytes and/or allelically methylated in tissues, and monoallelic KBTBD6 expression was observed, indicating livestock-specific imprinting. Further analysis revealed that these CpG islands were embedded within transcripts in porcine and bovine oocytes which coexisted with an active transcription mark and DNA methylation, implying the presence of transcription-dependent imprinting.

Conclusions: In this study, our comparative approach revealed an imprinted expression of the KBTBD6 gene in domesticated mammals, but not in humans, non-human primates, and mice which implicates species-specific evolution of genomic imprinting.

Abstract Image

Abstract Image

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KBTBD6基因座的印迹涉及家畜中物种特异性母体甲基化和单等位基因表达。
背景:母体超甲基化的初级差异甲基化区(DMRs)作为驱动单等位基因表达的印迹控制区(ICRs),这些ICRs因其在哺乳动物发育中的意义而被研究。尽管有一部分基因已被鉴定为印迹基因,但需要开发深入的比较方法来鉴定物种特异性印迹基因。在这里,我们检测了物种和组织中KBTBD6基因座的DNA甲基化状态和等位基因表达,并探索了印迹的潜在机制。结果:通过对孤雌生殖和正常猪胚胎进行亚硫酸氢盐全基因组测序和RNA测序,我们在KBTBD6启动子CpG岛上鉴定了胚胎之间的母系高甲基化DMR和KBTBD6的父系单等位基因表达。此外,在分析的驯养哺乳动物中,但在人类、非人灵长类动物和小鼠中没有,KBTBD6启动子CpG岛在卵母细胞中被甲基化和/或在组织中被等位基因甲基化,并且观察到单等位基因KBTBD6的表达,表明牲畜特异性印迹。进一步的分析显示,这些CpG岛嵌入猪和牛卵母细胞的转录物中,与活性转录标记和DNA甲基化共存,这意味着存在转录依赖性印迹。结论:在这项研究中,我们的比较方法揭示了KBTBD6基因在驯养哺乳动物中的印迹表达,但在人类、非人灵长类动物和小鼠中没有,这表明基因组印迹的物种特异性进化。
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来源期刊
CiteScore
10.30
自引率
0.00%
发文量
822
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