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[利用一种新方法——有序差异显示克隆涡虫区域特异性遗传标记]

[Cloning of region-specific genetic markers of planaria using a new method--ordered differential display].

作者信息

Mats M V, Shagin D A, Usman N Iu, Bogdanova E A, Fradkov A F, Soboleva T A, Luk'ianov S A

机构信息

Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, Moscow, Russia.

出版信息

Bioorg Khim. 1998 Dec;24(12):910-5.

Abstract

A new method for finding differentially expressed genes, termed ordered differential display of mRNAs (ODD), was used in the search for region-specific molecular markers of freshwater planarian Dugesia tigrina. In this method, the effect of selective suppression of a polymerase chain reaction (PCR) is used for the differential amplification of a pool of 3'-terminal cDNA fragments generated by digestion of cDNAs with a restriction endonuclease. In the resulting amplified cDNAs, every mRNA is represented by a cDNA fragment whose length is determined by the position of the restriction site nearest to the 3'-terminus. Subsequent PCR with primers 3'-extended by two random nucleotides allowed the amplification of 1/192 part of all cDNA molecules present in the sample. The comparison of the generated pools of cDNA molecules separated by PAGE leads to the identification of differentially expressed sequences. The systematic study of the total mRNA pool is achieved by the successive use of all possible combinations of extended primers. Some sequences preferentially expressed along the anterior-posterior axis of planarian were identified using ODD.

摘要

一种寻找差异表达基因的新方法,称为mRNA有序差异显示(ODD),被用于寻找淡水涡虫杜氏虎纹涡虫区域特异性分子标记。在该方法中,利用聚合酶链反应(PCR)的选择性抑制作用,对用限制性内切酶消化cDNA产生的3'-末端cDNA片段池进行差异扩增。在所得的扩增cDNA中,每个mRNA由一个cDNA片段代表,其长度由最接近3'-末端的限制性位点的位置决定。随后用两个随机核苷酸3'-延伸的引物进行PCR,可扩增样品中所有cDNA分子的1/192部分。通过PAGE分离产生的cDNA分子池的比较,可鉴定差异表达序列。通过连续使用延伸引物的所有可能组合,实现了对总mRNA池的系统研究。利用ODD鉴定了一些沿涡虫前后轴优先表达的序列。

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