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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Main Authors: Liu, Q., Hill, P.J., Karamitri, Angeliki, Ryan, K.J.P., Chen, H.Y., Lomax, Michael A.
Format: Article
Published: Elsevier 2013
Subjects:
Online Access:https://eprints.nottingham.ac.uk/3158/
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author Liu, Q.
Hill, P.J.
Karamitri, Angeliki
Ryan, K.J.P.
Chen, H.Y.
Lomax, Michael A.
author_facet Liu, Q.
Hill, P.J.
Karamitri, Angeliki
Ryan, K.J.P.
Chen, H.Y.
Lomax, Michael A.
author_sort Liu, Q.
building Nottingham Research Data Repository
collection Online Access
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 nottingham-31582020-05-04T20:19:42Z https://eprints.nottingham.ac.uk/3158/ Construction of a doxycycline inducible adipogenic lentiviral expression system Liu, Q. Hill, P.J. Karamitri, Angeliki Ryan, K.J.P. Chen, H.Y. Lomax, Michael A. 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. Elsevier 2013-01 Article PeerReviewed Liu, Q., Hill, P.J., Karamitri, Angeliki, Ryan, K.J.P., Chen, H.Y. and Lomax, Michael A. (2013) Construction of a doxycycline inducible adipogenic lentiviral expression system. Plasmid, 69 (1). pp. 96-103. ISSN 0147-619X Tetracycline inducible expression; Lentiviral plasmid; Adipose-specific promoter; Adipocyte http://www.sciencedirect.com/science/article/pii/S0147619X12001060 doi:10.1016/j.plasmid.2012.10.001 doi:10.1016/j.plasmid.2012.10.001
spellingShingle Tetracycline inducible expression; Lentiviral plasmid; Adipose-specific promoter; Adipocyte
Liu, Q.
Hill, P.J.
Karamitri, Angeliki
Ryan, K.J.P.
Chen, H.Y.
Lomax, Michael 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 Tetracycline inducible expression; Lentiviral plasmid; Adipose-specific promoter; Adipocyte
url https://eprints.nottingham.ac.uk/3158/
https://eprints.nottingham.ac.uk/3158/
https://eprints.nottingham.ac.uk/3158/