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限制性内切酶指纹分析(REF):一种用于筛选长的连续DNA片段中突变的灵敏方法。

Restriction endonuclease fingerprinting (REF): a sensitive method for screening mutations in long, contiguous segments of DNA.

作者信息

Liu Q, Sommer S S

机构信息

Mayo Clinic/Foundation, Rochester, MN, USA.

出版信息

Biotechniques. 1995 Mar;18(3):470-7.

PMID:7779398
Abstract

Restriction endonuclease fingerprinting (REF) is a modification of single-strand confirmation polymorphism (SSCP) that was developed to detect the presence of essentially all mutations in a 1-kb segment. To test REF, a 1-kb segment of the human factor IX gene was amplified with PCR and digested with each of five groups of restriction endonucleases. The endonucleases in each group were chosen so that the average size of the fragments was about 150 bp. After separate digestions, the products were mixed, 5' end-labeled with T4 polynucleotide kinase, denatured and electrophoresed under nondenaturing conditions. Each lane screened 1 kb and typically contained 68 segments (6.8 fragments per average digestion x 5 digestions x 2 strands). REF was performed with 5.6% polyacrylamide and 7.5% GeneAmp at temperatures of either 23 degrees or 8 degrees C. Point mutations resulted in the gain or loss of a restriction site in 21% of 24 test mutations (informative restriction component). In cases in which the restriction component was not informative, mutations were detected if any of the five mutation-containing restriction fragments (producing 10 single-stranded segments) displayed abnormal mobility (SSCP component). The average efficiency per single-stranded segment of the SSCP component for the 24 point mutations ranged from 49% for polyacrylamide at 23 degrees C to 68% with GeneAmp at 8 degrees C. REF detected 96% of the mutations with polyacrylamide at 23 degrees C and 100% with GeneAmp at 23 degrees or 8 degrees C. GeneAmp at 23 degrees and 8 degrees C also detected 100% of a subsequent blinded sample that contained normal controls and 27 different point mutations.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

限制性内切酶指纹图谱(REF)是单链构象多态性(SSCP)的一种改良方法,其开发目的是检测1kb片段中几乎所有突变的存在。为了测试REF,用聚合酶链反应(PCR)扩增人凝血因子IX基因的1kb片段,并用五组限制性内切酶中的每一组进行消化。每组中的内切酶经过挑选,使得片段的平均大小约为150bp。单独消化后,将产物混合,用T4多核苷酸激酶进行5'端标记,变性并在非变性条件下进行电泳。每条泳道检测1kb,通常包含68个片段(每次平均消化6.8个片段×5次消化×2条链)。REF在5.6%聚丙烯酰胺和7.5%GeneAmp中于23℃或8℃进行。在24个测试突变中有21%(信息性限制性成分)的点突变导致限制性位点的获得或丧失。在限制性成分无信息的情况下,如果五个含突变的限制性片段(产生10个单链片段)中的任何一个显示异常迁移率(SSCP成分),则可检测到突变。对于24个点突变,SSCP成分的每个单链片段的平均效率范围为23℃聚丙烯酰胺时的49%至8℃GeneAmp时的68%。REF在23℃聚丙烯酰胺时检测到96%的突变,在23℃或8℃GeneAmp时检测到100%的突变。23℃和8℃的GeneAmp也检测到了后续包含正常对照和27个不同点突变的盲样中的100%的突变。(摘要截短于250字)

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