Bile acid-controlled transgene expression in mammalian cells and mice

被引:18
作者
Roessger, Katrin [1 ]
Charpin-El-Hamri, Ghislaine [2 ]
Fussenegger, Martin [1 ,3 ]
机构
[1] Swiss Fed Inst Technol, Dept Biosyst Sci & Engn, CH-4058 Basel, Switzerland
[2] Inst Univ Technol IUTA, Dept Genie Biol, F-69622 Villeurbanne, France
[3] Univ Basel, Fac Sci, CH-4058 Basel, Switzerland
基金
欧洲研究理事会;
关键词
Synthetic biology; Gene switch; Gene circuit; Gene expression; PRODUCT GENE-EXPRESSION; MULTIDRUG EFFLUX PUMP; INTRAHEPATIC CHOLESTASIS; CAMPYLOBACTER-JEJUNI; TRANSCRIPTION; CMEABC; CMER; REPRESSOR; CIRCUIT; SWITCH;
D O I
10.1016/j.ymben.2013.11.003
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
In recent years, using trigger-inducible mammalian gene switches to design sophisticated transcription-control networks has become standard practice in synthetic biology. These switches provide unprecedented precision, complexity and reliability when programming novel mammalian cell functions. Metabolite-responsive repressors of human-pathogenic bacteria are particularly attractive for use in these orthogonal synthetic mammalian gene switches because the trigger compound sensitivity often matches the human physiological range. We have designed both a bile acid-repressible (BEAR(OFF)) as well as a bile-acid-inducible (BEAR(ON)) gene switch by capitalizing on components that have evolved to manage bile acid resistance in Campylobacter jejuni, the leading causative agent of human food-borne enteritis. We have shown that both of these switches enable bile acid-adjustable transgene expression in different mammalian cell lines as well as in mice. For the BEAR(OFF) device, the C jejuni repressor CmeR was fused to the VP16 transactivation domain to create a synthetic transactivator that activates minimal promoters containing tandem operator modules (O-cme) in a bile acid-repressible manner. Fusion of CmeR to a transsilencing domain resulted in an artificial transsilencer that binds and represses a constitutive O-cme-containing promoter until it is released by addition of bile acid (BEAR(ON)). A tailored multi-step tuning program for the inducible gene switch, which included the optimization of individual component performance, control of their relative abundances, the choice of the cell line and trigger compound, resulted in a BEAR(ON) device with significantly improved bile acid responsive control characteristics. Synthetic metabolite triggered gene switches that are able to interface with host metabolism may foster advances in future gene and cell based therapies. (C) 2013 International Metabolic Engineering Society. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:81 / 90
页数:10
相关论文
共 67 条
  • [1] From gene switches to mammalian designer cells: present and future prospects
    Auslaender, Simon
    Fussenegger, Martin
    [J]. TRENDS IN BIOTECHNOLOGY, 2013, 31 (03) : 155 - 168
  • [2] Programmable single-cell mammalian biocomputers
    Auslaender, Simon
    Auslaender, David
    Mueller, Marius
    Wieland, Markus
    Fussenegger, Martin
    [J]. NATURE, 2012, 487 (7405) : 123 - +
  • [3] Increasing the dynamic control space of mammalian transcription devices by combinatorial assembly of homologous regulatory elements from different bacterial species
    Bacchus, William
    Weber, Wilfried
    Fussenegger, Martin
    [J]. METABOLIC ENGINEERING, 2013, 15 : 144 - 150
  • [4] Synthetic two-way communication between mammalian cells
    Bacchus, William
    Lang, Moritz
    El-Baba, Marie Daoud
    Weber, Wilfried
    Stelling, Joerg
    Fussenegger, Martin
    [J]. NATURE BIOTECHNOLOGY, 2012, 30 (10) : 991 - +
  • [5] SERUM CONJUGATED BILE-ACID PROFILE DURING INH INTRAHEPATIC CHOLESTASIS OF PREGNANCY
    BACQ, Y
    MYARA, A
    BRECHOT, MC
    HAMON, C
    STUDER, E
    TRIVIN, F
    METMAN, EH
    [J]. JOURNAL OF HEPATOLOGY, 1995, 22 (01): : 66 - 70
  • [6] Control of the establishment of aversive memory by calcineurin and Zif268
    Baumgaertel, Karsten
    Genoux, David
    Welzl, Hans
    Tweedie-Cullen, Ry Y.
    Koshibu, Kyoko
    Livingstone-Zatchej, Magdalena
    Mamie, Celine
    Mansuy, Isabelle M.
    [J]. NATURE NEUROSCIENCE, 2008, 11 (05) : 572 - 578
  • [7] Specific host genes required for the killing of Klebsiella bacteria by phagocytes
    Benghezal, M
    Fauvarque, MO
    Tournebize, R
    Froquet, R
    Marchetti, A
    Bergeret, E
    Lardy, B
    Klein, G
    Sansonetti, P
    Charette, SJ
    Cosson, P
    [J]. CELLULAR MICROBIOLOGY, 2006, 8 (01) : 139 - 148
  • [8] Regulation of the expression of the CmeABC efflux pump in Campylobacter jejuni:: identification of a point mutation abolishing the binding of the CmeR repressor in an in vitro-selected multidrug-resistant mutant
    Cagliero, Cedric
    Maurel, Marie-Christine
    Cloeckaert, Axel
    Payot, Sophie
    [J]. FEMS MICROBIOLOGY LETTERS, 2007, 267 (01) : 89 - 94
  • [9] Reprogramming Cellular Behavior with RNA Controllers Responsive to Endogenous Proteins
    Culler, Stephanie J.
    Hoff, Kevin G.
    Smolke, Christina D.
    [J]. SCIENCE, 2010, 330 (6008) : 1251 - 1255
  • [10] A tunable genetic switch based on RNAi and repressor proteins for regulating gene expression in mammalian cells
    Deans, Tara L.
    Cantor, Charles R.
    Collins, James J.
    [J]. CELL, 2007, 130 (02) : 363 - 372