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用于富含GC区域中metC/C位点特异性定量评估的单核苷酸延伸技术。

Single nucleotide extension technology for quantitative site-specific evaluation of metC/C in GC-rich regions.

作者信息

Kaminsky Zachary A, Assadzadeh Abbas, Flanagan James, Petronis Arturas

机构信息

The Krembil Family Epigenetics Laboratory, Centre for Addiction and Mental Health Toronto, ON, Canada M5T 1R8.

出版信息

Nucleic Acids Res. 2005 Jun 15;33(10):e95. doi: 10.1093/nar/gni094.

Abstract

The development and use of high throughput technologies for detailed mapping of methylated cytosines (metC) is becoming of increasing importance for the expanding field of epigenetics. The single nucleotide primer extension reaction used for genotyping of single nucleotide polymorphisms has been recently adapted to interrogate the bisulfite modification induced 'quantitative' C/T polymorphism that corresponds to metC/C in the native DNA. In this study, we explored the opportunity to investigate C/T (and G/A) ratios using the Applied Biosystems (ABI) SNaPshot technology. The main effort of this study was dedicated to addressing the complexities in the analysis of DNA methylation in GC-rich regions where interrogation of the target cytosine can be confounded by variable degrees of methylation in other cytosines (resulting in variable C/T or G/A ratios after treatment with bisulfite) in the annealing site of the interrogating primer. In our studies, the mismatches of the SNaPshot primer with the target DNA sequence resulted in a biasing effect of up to 70% while these effects decreased as the location of the polymorphic site moved upstream of the target cytosine. We demonstrated that the biasing effect can be corrected with the SNaPshot primers containing degenerative C/T and G/A nucleotides. A series of experiments using various permutations of quantitative C/T and G/A polymorphisms at various positions of the target DNA sequence demonstrated that SNaPshot is able to accurately report cytosine methylation levels with <5% average SD from the true values. Given the relative simplicity of the method and the possibility to multiplex C/T and G/A interrogations, the SNaPshot approach may become a useful tool for large-scale mapping of metC.

摘要

对于不断发展的表观遗传学领域而言,开发和使用用于详细绘制甲基化胞嘧啶(metC)图谱的高通量技术正变得越来越重要。用于单核苷酸多态性基因分型的单核苷酸引物延伸反应最近已被改编,用于检测亚硫酸氢盐修饰诱导的“定量”C/T多态性,该多态性与天然DNA中的metC/C相对应。在本研究中,我们探索了使用应用生物系统公司(ABI)的SNaPshot技术研究C/T(和G/A)比率的机会。本研究的主要工作致力于解决富含GC区域DNA甲基化分析中的复杂性,在该区域,靶向胞嘧啶的检测可能会因在检测引物退火位点的其他胞嘧啶的不同程度甲基化(导致亚硫酸氢盐处理后C/T或G/A比率可变)而混淆。在我们的研究中,SNaPshot引物与目标DNA序列的错配导致高达70%的偏差效应,而随着多态性位点位置向上游移动到目标胞嘧啶,这些效应会降低。我们证明,可以用含有简并C/T和G/A核苷酸的SNaPshot引物校正偏差效应。在目标DNA序列的不同位置使用定量C/T和G/A多态性的各种排列进行的一系列实验表明,SNaPshot能够准确报告胞嘧啶甲基化水平,平均标准差与真实值的偏差<5%。鉴于该方法相对简单,并且有可能对C/T和G/A检测进行多重分析,SNaPshot方法可能成为大规模绘制metC图谱的有用工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2a8/1150895/e1a98b2760d3/gni094f1.jpg

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