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Universal endogenous gene controls for bisulphite conversion in analysis of plant DNA methylation

机译:亚硫酸氢盐转化的通用内源基因控制用于植物DNA甲基化分析

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摘要

Accurate analysis of DNA methylation by bisulphite sequencing depends on the complete conversion of all cytosines into uracil. Until now there has been no standard or universal gene identified as an endogenous control to monitor the conversion frequency in plants. Here, we report the development of PCR based assays for one nuclear gene IND (INDEHISCENT) and two mitochondrial genes, NAD (NICOTINAMIDE ADENINE DINUCLEOTIDE) and ATP1 (ATPase SUBUNIT 1). We demonstrated their efficacy as bisulphite conversion controls in Brassica and other plant taxa. The target regions amplified by four primer pairs were found to be consistently free from DNA methylation. Primer pairs for IND.a and NAD were effective within Brassica species, whereas two primer pairs for ATP1 provided reliable controls across a representative range of dicot and monocot angiosperm species. These primer sets may therefore be adopted as controls in plant methylation analysis for a wide range of studies.
机译:亚硫酸氢盐测序对DNA甲基化的准确分析取决于所有胞嘧啶是否完全转化为尿嘧啶。迄今为止,还没有标准或通用基因被鉴定为监测植物转化频率的内源性对照。在这里,我们报告了一个核基因IND(INDEHISCENT)和两个线粒体基因NAD(NICOTINAMIDE ADENINE DINUCLEOTIDE)和ATP1(ATPase SUBUNIT 1)的基于PCR的检测方法的开发。我们证明了它们作为芸苔属和其他植物类群中亚硫酸氢盐转化对照的功效。发现通过四个引物对扩增的靶区域始终没有DNA甲基化。芸苔属物种中IND.a和NAD的引物对有效,而ATP1的两个引物对在双子叶植物和单子叶植物被子植物的代表性范围内提供了可靠的对照。因此,这些引物组可以用作植物甲基化分析的对照,以进行广泛的研究。

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