a) a genomic DNA sample is treated with sulfite or disulfite in such a way that all of the cytosine bases that are not methylated in the 5-position of the base are changed in such a way that a base is formed that is different in its base-pairing behavior, whereas the cytosines methylated at the 5-position remain unchanged, andb) an aliquot of the same genomic DNA sample is quantitatively methylated with Sss1 or another methyltransferase prior to the chemical treatment according to a) andc) both of the DNA samples treated in this way are investigated for the presence of cytosine by means of the same analytical method, andd) the cytosine positions that are determined are matched with a reference DNA sequence."/> Method for distinguishing 5-position methylation changes of cytosine bases and cytosine-to-thymine mutations and for detecting single nucleotide polymorphisms (SNPs) or point mutations in genomic DNA
首页> 外国专利> Method for distinguishing 5-position methylation changes of cytosine bases and cytosine-to-thymine mutations and for detecting single nucleotide polymorphisms (SNPs) or point mutations in genomic DNA

Method for distinguishing 5-position methylation changes of cytosine bases and cytosine-to-thymine mutations and for detecting single nucleotide polymorphisms (SNPs) or point mutations in genomic DNA

机译:区分胞嘧啶碱基和胞嘧啶-胸腺嘧啶突变的5-位甲基化变化并检测基因组DNA中单核苷酸多态性(SNP)或点突变的方法

摘要

A method is described for distinguishing 5-position methylation changes of cytosine bases and cytosine-to-thymine mutations and for the detection of single nucleotide polymorphisms (SNPs) or point mutations in genomic DNA, in which:a) a genomic DNA sample is treated with sulfite or disulfite in such a way that all of the cytosine bases that are not methylated in the 5-position of the base are changed in such a way that a base is formed that is different in its base-pairing behavior, whereas the cytosines methylated at the 5-position remain unchanged, andb) an aliquot of the same genomic DNA sample is quantitatively methylated with Sss1 or another methyltransferase prior to the chemical treatment according to a) andc) both of the DNA samples treated in this way are investigated for the presence of cytosine by means of the same analytical method, andd) the cytosine positions that are determined are matched with a reference DNA sequence.
机译:描述了一种区分胞嘧啶碱基和胞嘧啶至胸腺嘧啶突变的5位甲基化变化以及检测基因组DNA中单核苷酸多态性(SNP)或点突变的方法,其中: a)用亚硫酸盐或亚硫酸氢盐处理基因组DNA样品,以使所有在碱基的5位未甲基化的胞嘧啶碱基都发生改变,从而使碱基变为形成的碱基配对行为不同,而在5位甲基化的胞嘧啶保持不变,并且 b)在按照a)和 c)进行化学处理之前,用Sss1或另一种甲基转移酶对基因组DNA样品进行定量甲基化处理通过相同的分析方法研究胞嘧啶的存在方式,并且 d)确定的胞嘧啶位置与参考DNA序列匹配。

著录项

  • 公开/公告号US7179594B1

    专利类型

  • 公开/公告日2007-02-20

    原文格式PDF

  • 申请/专利权人 KURT BERLIN;

    申请/专利号US20000110610

  • 发明设计人 KURT BERLIN;

    申请日2000-10-13

  • 分类号C12Q1/68;C12P19/34;C07H21/02;C07H21/04;

  • 国家 US

  • 入库时间 2022-08-21 21:00:34

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