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Study on the application of parent-of-origin specific DNA methylation markers to forensic genetics.

机译:母本特异性DNA甲基化标记在法医遗传学中的应用研究。

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In paternity test, especially in motherless cases, the allele inherited from father (obligatory gene, OG) often cannot be determined. The paternity exclusion probability (PE) of a genetic marker is reduced considerably. Therefore, it is necessary to develop a new technique, by which the parental origin of alleles can be determined without genealogical analysis. In this paper, we explored the possibility of using parent-of-origin specific DNA methylation markers to determine the parental origin of alleles, choosing the imprinted single nucleotide polymorphism (SNP) locus rs220028 (A/G) as a model system. We typed the SNP by mutagenically separated PCR (MS-PCR). The frequencies of alleles were A=0.5085, G=0.4915; the unbiased heterozygosity was 0.5020. In order to discriminate between the maternal allele and paternal allele, post-digestion MS-PCR, a novel PCR based methylation analysis and SNP typing technique was developed and performed on 18 heterozygous children, and the methylated maternal allele wasdetected specifically. As a pilot study on the use of epigenetic markers in forensic genetics, our results demonstrated the feasibility of using parent-of-origin specific DNA methylation markers to determine the parental origin of alleles.
机译:在亲子鉴定中,尤其是在没有母亲的情况下,通常无法确定从父亲遗传的等位基因(强制性基因,OG)。遗传标记的父子排斥概率(PE)大大降低。因此,有必要开发一种新技术,通过该新技术无需进行族谱分析即可确定等位基因的亲本来源。在本文中,我们探索了使用起源父母的特定DNA甲基化标记物确定等位基因的父母起源的可能性,选择印迹单核苷酸多态性(SNP)基因座rs220028(A / G)作为模型系统。我们通过诱变分离PCR(MS-PCR)输入了SNP。等位基因频率为A = 0.5085,G = 0.4915;无偏杂合度为0.5020。为了区分母体等位基因和父本等位基因,对消化后的MS-PCR进行了研究,开发了一种基于PCR的新型甲基化分析和SNP分型技术,并对18名杂合儿童进行了检测,并专门检测了甲基化的母体等位基因。作为在法医遗传学中使用表观遗传标记的一项初步研究,我们的结果证明了使用起源父母的特定DNA甲基化标记来确定等位基因的父母起源的可行性。

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