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{"title":"Transposon Insertion Site Sequencing (TIS-Seq): An Efficient and High-Throughput Method for Determining Transposon Insertion Site(s) and Their Relative Abundances in a PiggyBac Transposon Mutant Pool by Next-Generation Sequencing.","authors":"Yaligara Veeranagouda, Michel Didier","doi":"10.1002/cpmb.47","DOIUrl":null,"url":null,"abstract":"<p><p>The PiggyBac (PB) transposon has emerged as a novel mutagenesis tool for understanding gene function and for phenotypic screening in eukaryotes. Successful screening of PB transposon mutants relies on efficient identification of transposon insertion site(s) (TIS) in mutant cells. However, currently available methods suffer from time-consuming steps. Here, we present the method for transposon insertion site sequencing (TIS-Seq) for high-throughput identification of TIS in transposon mutants. TIS-Seq provides qualitative and quantitative information on mutants present in a given PB transposon mutant library. TIS-Seq also facilitates identification of TIS in up to 96 individual/hand-picked mutants in a single MiniSeq/MiSeq run. TIS-Seq is a versatile method that can be easily modified to identify TIS from any kind of transposon mutant, as long as one end of the DNA sequence is known. Therefore, TIS-Seq is a promising method for transposon mutant screening. © 2017 by John Wiley & Sons, Inc.</p>","PeriodicalId":10734,"journal":{"name":"Current Protocols in Molecular Biology","volume":"120 ","pages":"21.35.1-21.35.11"},"PeriodicalIF":0.0000,"publicationDate":"2017-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cpmb.47","citationCount":"7","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols in Molecular Biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/cpmb.47","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
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Abstract
The PiggyBac (PB) transposon has emerged as a novel mutagenesis tool for understanding gene function and for phenotypic screening in eukaryotes. Successful screening of PB transposon mutants relies on efficient identification of transposon insertion site(s) (TIS) in mutant cells. However, currently available methods suffer from time-consuming steps. Here, we present the method for transposon insertion site sequencing (TIS-Seq) for high-throughput identification of TIS in transposon mutants. TIS-Seq provides qualitative and quantitative information on mutants present in a given PB transposon mutant library. TIS-Seq also facilitates identification of TIS in up to 96 individual/hand-picked mutants in a single MiniSeq/MiSeq run. TIS-Seq is a versatile method that can be easily modified to identify TIS from any kind of transposon mutant, as long as one end of the DNA sequence is known. Therefore, TIS-Seq is a promising method for transposon mutant screening. © 2017 by John Wiley & Sons, Inc.
转座子插入位点测序(TIS-Seq):利用新一代测序技术测定PiggyBac转座子突变体库中转座子插入位点及其相对丰度的高效、高通量方法。
PiggyBac (PB)转座子已成为一种新的突变工具,用于了解真核生物的基因功能和表型筛选。PB转座子突变体的成功筛选依赖于突变细胞中转座子插入位点(TIS)的有效鉴定。然而,目前可用的方法存在耗时的问题。在这里,我们提出了转座子插入位点测序(TIS- seq)方法,用于高通量鉴定转座子突变体中的TIS。TIS-Seq提供了在给定的PB转座子突变文库中存在的突变体的定性和定量信息。TIS- seq还有助于在单次MiniSeq/MiSeq中鉴定多达96个单独/精心挑选的突变体的TIS。TIS- seq是一种通用的方法,可以很容易地从任何转座子突变体中识别出TIS,只要DNA序列的一端是已知的。因此,TIS-Seq是一种很有前途的转座子突变体筛选方法。©2017 by John Wiley & Sons, Inc。
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