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- Publisher Website: 10.1126/science.1193004
- Scopus: eid_2-s2.0-78449294626
- PMID: 20947725
- WOS: WOS:000284374700044
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Article: PiggyBac transposon mutagenesis: A tool for cancer gene discovery in mice
Title | PiggyBac transposon mutagenesis: A tool for cancer gene discovery in mice |
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Authors | |
Issue Date | 2010 |
Citation | Science, 2010, v. 330, n. 6007, p. 1104-1107 How to Cite? |
Abstract | Transposons are mobile DNA segments that can disrupt gene function by inserting in or near genes. Here, we show that insertional mutagenesis by the PiggyBac transposon can be used for cancer gene discovery in mice. PiggyBac transposition in genetically engineered transposon-transposase mice induced cancers whose type (hematopoietic versus solid) and latency were dependent on the regulatory elements introduced into transposons. Analysis of 63 hematopoietic tumors revealed that PiggyBac is capable of genome-wide mutagenesis. The PiggyBac screen uncovered many cancer genes not identified in previous retroviral or Sleeping Beauty transposon screens, including Spic, which encodes a PU.1-related transcription factor, and Hdac7, a histone deacetylase gene. PiggyBac and Sleeping Beauty have different integration preferences. Tomaximize the utility of the tool, we engineered 21 mouse lines to be compatible with both transposon systems in constitutive, tissue- or temporal-specific mutagenesis. Mice with different transposon types, copy numbers, and chromosomal locations support wide applicability. |
Persistent Identifier | http://hdl.handle.net/10722/249044 |
ISSN | 2023 Impact Factor: 44.7 2023 SCImago Journal Rankings: 11.902 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Rad, Roland | - |
dc.contributor.author | Rad, Lena | - |
dc.contributor.author | Wang, Wei | - |
dc.contributor.author | Cadinanos, Juan | - |
dc.contributor.author | Vassiliou, George | - |
dc.contributor.author | Rice, Stephen | - |
dc.contributor.author | Campos, Lia S. | - |
dc.contributor.author | Yusa, Kosuke | - |
dc.contributor.author | Banerjee, Ruby | - |
dc.contributor.author | Li, Meng Amy | - |
dc.contributor.author | De La Rosa, Jorge | - |
dc.contributor.author | Strong, Alexander | - |
dc.contributor.author | Lu, Dong | - |
dc.contributor.author | Ellis, Peter | - |
dc.contributor.author | Conte, Nathalie | - |
dc.contributor.author | Yang, Fang Tang | - |
dc.contributor.author | Liu, Pentao | - |
dc.contributor.author | Bradley, Allan | - |
dc.date.accessioned | 2017-10-27T05:58:57Z | - |
dc.date.available | 2017-10-27T05:58:57Z | - |
dc.date.issued | 2010 | - |
dc.identifier.citation | Science, 2010, v. 330, n. 6007, p. 1104-1107 | - |
dc.identifier.issn | 0036-8075 | - |
dc.identifier.uri | http://hdl.handle.net/10722/249044 | - |
dc.description.abstract | Transposons are mobile DNA segments that can disrupt gene function by inserting in or near genes. Here, we show that insertional mutagenesis by the PiggyBac transposon can be used for cancer gene discovery in mice. PiggyBac transposition in genetically engineered transposon-transposase mice induced cancers whose type (hematopoietic versus solid) and latency were dependent on the regulatory elements introduced into transposons. Analysis of 63 hematopoietic tumors revealed that PiggyBac is capable of genome-wide mutagenesis. The PiggyBac screen uncovered many cancer genes not identified in previous retroviral or Sleeping Beauty transposon screens, including Spic, which encodes a PU.1-related transcription factor, and Hdac7, a histone deacetylase gene. PiggyBac and Sleeping Beauty have different integration preferences. Tomaximize the utility of the tool, we engineered 21 mouse lines to be compatible with both transposon systems in constitutive, tissue- or temporal-specific mutagenesis. Mice with different transposon types, copy numbers, and chromosomal locations support wide applicability. | - |
dc.language | eng | - |
dc.relation.ispartof | Science | - |
dc.title | PiggyBac transposon mutagenesis: A tool for cancer gene discovery in mice | - |
dc.type | Article | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1126/science.1193004 | - |
dc.identifier.pmid | 20947725 | - |
dc.identifier.scopus | eid_2-s2.0-78449294626 | - |
dc.identifier.volume | 330 | - |
dc.identifier.issue | 6007 | - |
dc.identifier.spage | 1104 | - |
dc.identifier.epage | 1107 | - |
dc.identifier.eissn | 1095-9203 | - |
dc.identifier.isi | WOS:000284374700044 | - |
dc.identifier.issnl | 0036-8075 | - |