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非CpG甲基化使亚硫酸氢盐PCR偏向于低甲基化或未甲基化的线粒体DNA:该领域的建议

Non-CpG methylation biases bisulphite PCR towards low or unmethylated mitochondrial DNA: recommendations for the field.

作者信息

Morris Margaret J, Hesson Luke B, Youngson Neil A

机构信息

School of Medical Sciences, UNSW Sydney, NSW 2052, Australia.

Prince of Wales Clinical School and Lowy Cancer Research Centre, UNSW Sydney, NSW 2052, Australia.

出版信息

Environ Epigenet. 2020 Feb 4;6(1):dvaa001. doi: 10.1093/eep/dvaa001. eCollection 2020 Jan.

Abstract

Mitochondrial DNA (mtDNA) is a circular genome of 16 kb that is present in multiple copies in mitochondria. mtDNA codes for genes that contribute to mitochondrial structure and function. A long-standing question has asked whether mtDNA is epigenetically regulated similarly to the nuclear genome. Recently published data suggest that unlike the nuclear genome where CpG methylation is the norm, mtDNA is methylated predominantly at non-CpG cytosines. This raises important methodological considerations for future investigations. In particular, existing bisulphite PCR techniques may be unsuitable due to primers being biased towards amplification from unmethylated mtDNA. Here, we describe how this may have led to previous studies underestimating the level of mtDNA methylation and reiterate methodological strategies for its accurate assessment.

摘要

线粒体DNA(mtDNA)是一个16kb的环状基因组,在线粒体中以多个拷贝存在。mtDNA编码有助于线粒体结构和功能的基因。一个长期存在的问题是,mtDNA是否像核基因组一样受到表观遗传调控。最近发表的数据表明,与以CpG甲基化为常态的核基因组不同,mtDNA主要在非CpG胞嘧啶处发生甲基化。这为未来的研究提出了重要的方法学考量。特别是,现有的亚硫酸氢盐PCR技术可能不合适,因为引物倾向于从未甲基化的mtDNA进行扩增。在这里,我们描述了这可能如何导致先前的研究低估了mtDNA甲基化水平,并重申了准确评估mtDNA甲基化的方法策略。

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