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Article: Generation of NSE-MerCreMer transgenic mice with tamoxifen inducible Cre activity in neurons
Title | Generation of NSE-MerCreMer transgenic mice with tamoxifen inducible Cre activity in neurons |
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Authors | |
Keywords | Cre recombinase Estrogen receptor Central nervous system Enzyme activity Enzyme induction |
Issue Date | 2012 |
Publisher | Public Library of Science. The Journal's web site is located at http://www.plosone.org/home.action |
Citation | Plos One, 2012, v. 7 n. 5 How to Cite? |
Abstract | To establish a genetic tool for conditional deletion or expression of gene in neurons in a temporally controlled manner, we generated a transgenic mouse (NSE-MerCreMer), which expressed a tamoxifen inducible type of Cre recombinase specifically in neurons. The tamoxifen inducible Cre recombinase (MerCreMer) is a fusion protein containing Cre recombinase with two modified estrogen receptor ligand binding domains at both ends, and is driven by the neural-specific rat neural specific enolase (NSE) promoter. A total of two transgenic lines were established, and expression of MerCreMer in neurons of the central and enteric nervous systems was confirmed. Transcript of MerCreMer was detected in several non-neural tissues such as heart, liver, and kidney in these lines. In the background of the Cre reporter mouse strain Rosa26R, Cre recombinase activity was inducible in neurons of adult NSE-MerCreMer mice treated with tamoxifen by intragastric gavage, but not in those fed with corn oil only. We conclude that NSE-MerCreMer lines will be useful for studying gene functions in neurons for the conditions that Cre-mediated recombination resulting in embryonic lethality, which precludes investigation of gene functions in neurons through later stages of development and in adult. © 2012 Kam et al. |
Persistent Identifier | http://hdl.handle.net/10722/149155 |
ISSN | 2023 Impact Factor: 2.9 2023 SCImago Journal Rankings: 0.839 |
PubMed Central ID | |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
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dc.contributor.author | Kam, MKM | en_HK |
dc.contributor.author | Lee, KY | en_HK |
dc.contributor.author | Tam, PKH | en_HK |
dc.contributor.author | Lui, VCH | en_HK |
dc.date.accessioned | 2012-06-22T06:27:01Z | - |
dc.date.available | 2012-06-22T06:27:01Z | - |
dc.date.issued | 2012 | en_HK |
dc.identifier.citation | Plos One, 2012, v. 7 n. 5 | en_HK |
dc.identifier.issn | 1932-6203 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/149155 | - |
dc.description.abstract | To establish a genetic tool for conditional deletion or expression of gene in neurons in a temporally controlled manner, we generated a transgenic mouse (NSE-MerCreMer), which expressed a tamoxifen inducible type of Cre recombinase specifically in neurons. The tamoxifen inducible Cre recombinase (MerCreMer) is a fusion protein containing Cre recombinase with two modified estrogen receptor ligand binding domains at both ends, and is driven by the neural-specific rat neural specific enolase (NSE) promoter. A total of two transgenic lines were established, and expression of MerCreMer in neurons of the central and enteric nervous systems was confirmed. Transcript of MerCreMer was detected in several non-neural tissues such as heart, liver, and kidney in these lines. In the background of the Cre reporter mouse strain Rosa26R, Cre recombinase activity was inducible in neurons of adult NSE-MerCreMer mice treated with tamoxifen by intragastric gavage, but not in those fed with corn oil only. We conclude that NSE-MerCreMer lines will be useful for studying gene functions in neurons for the conditions that Cre-mediated recombination resulting in embryonic lethality, which precludes investigation of gene functions in neurons through later stages of development and in adult. © 2012 Kam et al. | en_HK |
dc.language | eng | en_US |
dc.publisher | Public Library of Science. The Journal's web site is located at http://www.plosone.org/home.action | en_HK |
dc.relation.ispartof | PLoS ONE | en_HK |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.subject | Cre recombinase | - |
dc.subject | Estrogen receptor | - |
dc.subject | Central nervous system | - |
dc.subject | Enzyme activity | - |
dc.subject | Enzyme induction | - |
dc.title | Generation of NSE-MerCreMer transgenic mice with tamoxifen inducible Cre activity in neurons | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Tam, PKH: paultam@hkucc.hku.hk | en_HK |
dc.identifier.email | Lui, VCH: vchlui@hkucc.hku.hk | en_HK |
dc.identifier.authority | Tam, PKH=rp00060 | en_HK |
dc.identifier.authority | Lui, VCH=rp00363 | en_HK |
dc.description.nature | published_or_final_version | - |
dc.identifier.doi | 10.1371/journal.pone.0035799 | en_HK |
dc.identifier.pmid | 22586451 | - |
dc.identifier.pmcid | PMC3346737 | - |
dc.identifier.scopus | eid_2-s2.0-84860640071 | en_HK |
dc.identifier.hkuros | 200159 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-84860640071&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 7 | en_HK |
dc.identifier.issue | 5 | en_HK |
dc.identifier.eissn | 1932-6203 | - |
dc.identifier.isi | WOS:000305335000013 | - |
dc.publisher.place | United States | en_HK |
dc.identifier.scopusauthorid | Kam, MKM=36719044000 | en_HK |
dc.identifier.scopusauthorid | Lee, KY=37112403900 | en_HK |
dc.identifier.scopusauthorid | Tam, PKH=7202539421 | en_HK |
dc.identifier.scopusauthorid | Lui, VCH=7004231344 | en_HK |
dc.identifier.issnl | 1932-6203 | - |