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METHOD FOR PRODUCING SINGLE STRAND GENE TAG GROUP CONTAINING TRANSCRIPTION STARTING SITE

机译:包含转录起始位点的单基因组标签组的生产方法

摘要

PPROBLEM TO BE SOLVED: To provide a method for producing a single strand gene tag group reflective of a kind and a ratio of quantity of a base sequence group at the mRNA 5' terminal extracted from a eukaryotic cell, to provide a method for measuring an expression level of a gene in the eukaryotic cell including a process for hybridizing a solid phase on which a DNA or a RNA containing a transcription starting site is immobilized with the single strand gene tag group, and to provide a method for preparing a gene expression profile by integrating obtained information on gene expression. PSOLUTION: This single strand gene tag group reflective of the kind and the ratio of the quantity of the base sequence at the mRNA 5' terminal is produced by combining a method disclosed in a 5'SAGE method with a procedure for forming a double-stranded DNA into a single strand. Thus, it is found that the single strand gene tag group is effective for recognizing expression of a gene which targets an expression starting site, as a result of conducting hybridization with a DNA chip by using the tag group as a sample. Further, utilization of the single strand gene tag group makes it possible to conduct comprehensive expression analysis of a gene which targets various transcription starting sites. PCOPYRIGHT: (C)2007,JPO&INPIT
机译:解决的问题:提供一种产生反映从真核细胞中提取的mRNA 5'末端的碱基序列基团的种类和数量比的单链基因标签基团的方法,提供一种方法用于测量真核细胞中基因的表达水平的方法,包括使固相杂交的方法,该固相上固定有含有转录起始位点的DNA或RNA与单链基因标签基团,并提供了制备方法通过整合获得的有关基因表达的信息来进行基因表达谱分析。

解决方案:该单链基因标签组反映了5'SAGE方法中公开的方法与形成5'SAGE方法的程序相结合,可反映出mRNA 5'末端碱基序列的种类和数量比例。双链DNA变成单链。因此,发现通过使用标签组作为样品与DNA芯片进行杂交的结果,单链基因标签组对于识别靶向表达起始位点的基因的表达是有效的。此外,利用单链基因标签组可以对靶向各种转录起始位点的基因进行全面的表达分析。

版权:(C)2007,日本特许厅&INPIT

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