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首页> 外文期刊>BMC Molecular Biology >Mutation detection using ENDO1:application to disease diagnostics in humans and TILLING and Eco-TILLING in plants
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Mutation detection using ENDO1:application to disease diagnostics in humans and TILLING and Eco-TILLING in plants

机译:使用ENDO1进行突变检测:应用于人类疾病诊断以及植物的TILLING和Eco-TILLING

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摘要

Background Most enzymatic mutation detection methods are based on the cleavage of heteroduplex DNA by a mismatch-specific endonuclease at mismatch sites and the analysis of the digestion product on a DNA sequencer.Important limitations of these methods are the availability of a mismatch-specific endonuclease,their sensitivity in detecting one allele in pool of DNA,the cost of the analysis and the ease by which the technique could be implemented in a standard molecular biology laboratory. Results The co-agroinfiltration of ENDO1 and p19 constructs into N.benthamiana leaves allowed high level of transient expression of a mismatch-specific and sensitive endonuclease,ENDO1 from Arabidopsis thaliana.We demonstrate the broad range of uses of the produced enzyme in detection of mutations.In human,we report the diagnosis of the G1691A mutation in Leiden factor-V gene associated with venous thrombosis and the fingerprinting of HIV-1 quasispecies in patients subjected to antiretroviral treatments.In plants,we report the use of ENDO1 system for detection of mutant alleles of Retinoblastoma-related gene by TILLING in Pisum sativum and discovery of natural sequence variations by Eco-TILLING in Arabidopsis thaliana. Conclusions We introduce a cost-effective tool based on a simplified purification protocol of a mismatch-specific and sensitive endonuclease,ENDO1.Especially,we report the successful applications of ENDO1 in mutation diagnostics in humans,fingerprinting of complex population of viruses,and in TILLING and Eco-TILLING in plants.
机译:背景技术大多数酶促突变检测方法都是基于错配位点上的错配特异性内切核酸酶对异源双链DNA的切割以及在DNA测序仪上对消化产物的分析。这些方法的重要局限性是错配特异性内切核酸酶的可用性,它们在检测DNA池中一个等位基因时的灵敏度,分析的成本以及在标准分子生物学实验室中实施该技术的难易程度。结果将ENDO1和p19构建体共农业渗入N.benthamiana叶片中可以使瞬时表达的错配特异性敏感核酸内切酶拟南芥ENDO1高水平表达。我们证明了产生的酶在检测突变中的广泛用途在人类中,我们报告了接受抗逆转录病毒治疗的患者中的莱顿因子-V基因G1691A突变与静脉血栓形成相关的诊断以及HIV-1准种的指纹图谱。在植物中,我们报告了使用ENDO1系统检测豌豆中TILLING诱导成视网膜细胞瘤相关基因的突变等位基因,拟南芥中Eco-TILLING发现自然序列变异。结论我们引入了一种经济高效的工具,该工具基于错配特异性和敏感核酸内切酶ENDO1的简化纯化方案。特别是,我们报道了ENDO1在人类突变诊断,复杂病毒指纹图谱以及TILLING中的成功应用。和在植物中进行生态耕种。

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