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Book Chapter: PiggyBac Transposon-Based Insertional Mutagenesis in Mice

TitlePiggyBac Transposon-Based Insertional Mutagenesis in Mice
Authors
KeywordsPiggyBac transposon
Insertional mutagenesis
Forward genetic screen
QiSeq
Issue Date2019
PublisherHumana Press.
Citation
PiggyBac Transposon-Based Insertional Mutagenesis in Mice. In Starr, TK (Ed.), Cancer Driver Genes: Methods and Protocols, p. 171-183. New York, NY: Humana Press, 2019 How to Cite?
AbstractWhile sequencing and array-based studies are creating catalogues of genetic alterations in cancer, discriminating cancer drivers among the large sets of epigenetically, transcriptionally or posttranslationally dysregulated genes remains a challenge. Transposon-based genetic screening in mice has proven to be a powerful approach to address this challenge. Insertional mutagenesis directly flags biologically relevant genes and, combined with the transposon’s unique molecular fingerprint, facilitates the recovery of insertion sites. We have generated transgenic mouse lines harboring different versions of PiggyBac-based oncogenic transposons, which in conjunction with PiggyBac transposase mice can be used for whole-body or tissue-specific insertional mutagenesis screens. We have also developed QiSeq, a method for (semi-)quantitative transposon insertion site sequencing, which overcomes biasing limitations of previous library preparation methods. QiSeq can be used in multiplexed high-throughput formats for candidate cancer gene discovery and gives insights into the clonal distribution of insertions for the study of genetic tumor evolution.
Persistent Identifierhttp://hdl.handle.net/10722/305736
ISBN
Series/Report no.Methods in Molecular Biology ; 1907

 

DC FieldValueLanguage
dc.contributor.authorFriedrich, MJ-
dc.contributor.authorBronner, IF-
dc.contributor.authorLiu, P-
dc.contributor.authorBradley, A-
dc.contributor.authorRad, R-
dc.date.accessioned2021-10-20T10:13:36Z-
dc.date.available2021-10-20T10:13:36Z-
dc.date.issued2019-
dc.identifier.citationPiggyBac Transposon-Based Insertional Mutagenesis in Mice. In Starr, TK (Ed.), Cancer Driver Genes: Methods and Protocols, p. 171-183. New York, NY: Humana Press, 2019-
dc.identifier.isbn9781493989669-
dc.identifier.urihttp://hdl.handle.net/10722/305736-
dc.description.abstractWhile sequencing and array-based studies are creating catalogues of genetic alterations in cancer, discriminating cancer drivers among the large sets of epigenetically, transcriptionally or posttranslationally dysregulated genes remains a challenge. Transposon-based genetic screening in mice has proven to be a powerful approach to address this challenge. Insertional mutagenesis directly flags biologically relevant genes and, combined with the transposon’s unique molecular fingerprint, facilitates the recovery of insertion sites. We have generated transgenic mouse lines harboring different versions of PiggyBac-based oncogenic transposons, which in conjunction with PiggyBac transposase mice can be used for whole-body or tissue-specific insertional mutagenesis screens. We have also developed QiSeq, a method for (semi-)quantitative transposon insertion site sequencing, which overcomes biasing limitations of previous library preparation methods. QiSeq can be used in multiplexed high-throughput formats for candidate cancer gene discovery and gives insights into the clonal distribution of insertions for the study of genetic tumor evolution.-
dc.languageeng-
dc.publisherHumana Press.-
dc.relation.ispartofCancer Driver Genes: Methods and Protocols-
dc.relation.ispartofseriesMethods in Molecular Biology ; 1907-
dc.subjectPiggyBac transposon-
dc.subjectInsertional mutagenesis-
dc.subjectForward genetic screen-
dc.subjectQiSeq-
dc.titlePiggyBac Transposon-Based Insertional Mutagenesis in Mice-
dc.typeBook_Chapter-
dc.identifier.emailLiu, P: pliu88@hku.hk-
dc.identifier.authorityLiu, P=rp02328-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1007/978-1-4939-8967-6_14-
dc.identifier.pmid30543000-
dc.identifier.scopuseid_2-s2.0-85058597083-
dc.identifier.hkuros327374-
dc.identifier.spage171-
dc.identifier.epage183-
dc.publisher.placeNew York, NY-

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