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Construction of a doxycycline inducible adipogenic lentiviral expression system

To provide a tool for research on regulating adipocyte differentiation, tetracycline inducible (Tet on) lentiviral expression vectors under the control of an adipose-specific promoter were constructed. The lowest basal expression in the absence of doxycycline and most efficient dose-dependent, doxyc...

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Detalles Bibliográficos
Autores principales: Liu, Q., Hill, P.J., Karamitri, A., Ryan, K.J.P., Chen, H.Y., Lomax, M.A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academic Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3556778/
https://www.ncbi.nlm.nih.gov/pubmed/23099229
http://dx.doi.org/10.1016/j.plasmid.2012.10.001
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author Liu, Q.
Hill, P.J.
Karamitri, A.
Ryan, K.J.P.
Chen, H.Y.
Lomax, M.A.
author_facet Liu, Q.
Hill, P.J.
Karamitri, A.
Ryan, K.J.P.
Chen, H.Y.
Lomax, M.A.
author_sort Liu, Q.
collection PubMed
description To provide a tool for research on regulating adipocyte differentiation, tetracycline inducible (Tet on) lentiviral expression vectors under the control of an adipose-specific promoter were constructed. The lowest basal expression in the absence of doxycycline and most efficient dose-dependent, doxycycline-induced transient overexpression was observed using vectors constructed with a combination of Tetracycline Responsive Element (TRE) and reverse tetracycline-controlled TransActivator advanced (rtTAadv), transfected in white (3T3-L1) and brown (HIB-1B) preadipocytes cell lines. The results demonstrate that doxycycline adipogenic inducible expression can be achieved using a pLenti TRE / rtTA adv under the control of the truncated aP2 promoter in HIB-1B preadipocytes.
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spelling pubmed-35567782013-01-28 Construction of a doxycycline inducible adipogenic lentiviral expression system Liu, Q. Hill, P.J. Karamitri, A. Ryan, K.J.P. Chen, H.Y. Lomax, M.A. Plasmid Article To provide a tool for research on regulating adipocyte differentiation, tetracycline inducible (Tet on) lentiviral expression vectors under the control of an adipose-specific promoter were constructed. The lowest basal expression in the absence of doxycycline and most efficient dose-dependent, doxycycline-induced transient overexpression was observed using vectors constructed with a combination of Tetracycline Responsive Element (TRE) and reverse tetracycline-controlled TransActivator advanced (rtTAadv), transfected in white (3T3-L1) and brown (HIB-1B) preadipocytes cell lines. The results demonstrate that doxycycline adipogenic inducible expression can be achieved using a pLenti TRE / rtTA adv under the control of the truncated aP2 promoter in HIB-1B preadipocytes. Academic Press 2013-01 /pmc/articles/PMC3556778/ /pubmed/23099229 http://dx.doi.org/10.1016/j.plasmid.2012.10.001 Text en © 2013 Elsevier Inc. https://creativecommons.org/licenses/by/3.0/ Open Access under CC BY 3.0 (https://creativecommons.org/licenses/by/3.0/) license
spellingShingle Article
Liu, Q.
Hill, P.J.
Karamitri, A.
Ryan, K.J.P.
Chen, H.Y.
Lomax, M.A.
Construction of a doxycycline inducible adipogenic lentiviral expression system
title Construction of a doxycycline inducible adipogenic lentiviral expression system
title_full Construction of a doxycycline inducible adipogenic lentiviral expression system
title_fullStr Construction of a doxycycline inducible adipogenic lentiviral expression system
title_full_unstemmed Construction of a doxycycline inducible adipogenic lentiviral expression system
title_short Construction of a doxycycline inducible adipogenic lentiviral expression system
title_sort construction of a doxycycline inducible adipogenic lentiviral expression system
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3556778/
https://www.ncbi.nlm.nih.gov/pubmed/23099229
http://dx.doi.org/10.1016/j.plasmid.2012.10.001
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