Autonomous Bioluminescent Expression of the Bacterial Luciferase Gene Cassette (lux) in a Mammalian Cell Line

被引:96
作者
Close, Dan M. [1 ]
Patterson, Stacey S. [1 ]
Ripp, Steven [1 ]
Baek, Seung J. [2 ]
Sanseverino, John [1 ]
Sayler, Gary S. [1 ]
机构
[1] Univ Tennessee, Ctr Environm Biotechnol, Knoxville, TN 37932 USA
[2] Univ Tennessee, Coll Vet Med, Dept Pathobiol, Knoxville, TN 37932 USA
来源
PLOS ONE | 2010年 / 5卷 / 08期
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
IN-VIVO; CODON OPTIMIZATION; SACCHAROMYCES-CEREVISIAE; FIREFLY LUCIFERASES; FUSION; ALDEHYDE; LUMINESCENCE; EFFICIENCY; YEAST;
D O I
10.1371/journal.pone.0012441
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: The bacterial luciferase (lux) gene cassette consists of five genes (luxCDABE) whose protein products synergistically generate bioluminescent light signals exclusive of supplementary substrate additions or exogenous manipulations. Historically expressible only in prokaryotes, the lux operon was re-synthesized through a process of multi-bicistronic, codon-optimization to demonstrate for the first time self-directed bioluminescence emission in a mammalian HEK293 cell line in vitro and in vivo. Methodology/Principal Findings: Autonomous in vitro light production was shown to be 12-fold greater than the observable background associated with untransfected control cells. The availability of reduced riboflavin phosphate (FMNH2) was identified as the limiting bioluminescence substrate in the mammalian cell environment even after the addition of a constitutively expressed flavin reductase gene (frp) from Vibrio harveyi. FMNH2 supplementation led to a 151-fold increase in bioluminescence in cells expressing mammalian codon-optimized luxCDE and frp genes. When injected subcutaneously into nude mice, in vivo optical imaging permitted near instantaneous light detection that persisted independently for the 60 min length of the assay with negligible background. Conclusions/Significance: The speed, longevity, and self-sufficiency of lux expression in the mammalian cellular environment provides a viable and powerful alternative for real-time target visualization not currently offered by existing bioluminescent and fluorescent imaging technologies.
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页数:12
相关论文
共 33 条
[1]   FUSION OF LUXA AND LUXB AND ITS EXPRESSION IN ESCHERICHIA-COLI, SACCHAROMYCES-CEREVISIAE AND DROSOPHILA-MELANOGASTER [J].
ALMASHANU, S ;
MUSAFIA, B ;
HADAR, R ;
SUISSA, M ;
KUHN, J .
JOURNAL OF BIOLUMINESCENCE AND CHEMILUMINESCENCE, 1990, 5 (02) :89-97
[2]   Thermostability of Firefly Luciferases Affects Efficiency of Detection by In Vivo Bioluminescence [J].
Baggett, Brenda ;
Roy, Rupali ;
Momen, Shafinaz ;
Morgan, Sherif ;
Tisi, Laurence ;
Morse, David ;
Gillies, Robert J. .
MOLECULAR IMAGING, 2004, 3 (04) :324-332
[3]  
Barrett JW, 2006, VIRUS GENES, V33, P15, DOI 10.1007/s11262-005-0035-7
[4]   Optical imaging of Renilla luciferase reporter gene expression in living mice [J].
Bhaumik, S ;
Gambhir, SS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (01) :377-382
[5]   Whole-body fluorescence lifetime imaging of a tumor-targeted near-infrared molecular probe in mice [J].
Bloch, S ;
Lesage, F ;
McIntosh, L ;
Gandjbakhche, A ;
Liang, KX ;
Achilefu, S .
JOURNAL OF BIOMEDICAL OPTICS, 2005, 10 (05)
[6]   GROWTH AND LUMINESCENCE OF THE BACTERIUM XENORHABDUS-LUMINESCENS FROM A HUMAN WOUND [J].
COLEPICOLO, P ;
CHO, KW ;
POINAR, GO ;
HASTINGS, JW .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1989, 55 (10) :2601-2606
[7]   Photonic detection of bacterial pathogens in living hosts [J].
Contag, CH ;
Contag, PR ;
Mullins, JI ;
Spilman, SD ;
Stevenson, DK ;
Benaron, DA .
MOLECULAR MICROBIOLOGY, 1995, 18 (04) :593-603
[8]   Advances in vivo bioluminescence imaging of gene expression [J].
Contag, CH ;
Bachmann, MH .
ANNUAL REVIEW OF BIOMEDICAL ENGINEERING, 2002, 4 :235-260
[9]   CONVERSION OF ALDEHYDE TO ACID IN BACTERIAL BIOLUMINESCENT REACTION [J].
DUNN, DK ;
MICHALISZYN, GA ;
BOGACKI, IG ;
MEIGHEN, EA .
BIOCHEMISTRY, 1973, 12 (24) :4911-4918
[10]   BACTERIAL LUCIFERASE ALPHA-BETA FUSION PROTEIN IS FULLY ACTIVE AS A MONOMER AND HIGHLY SENSITIVE INVIVO TO ELEVATED-TEMPERATURE [J].
ESCHER, A ;
OKANE, DJ ;
LEE, J ;
SZALAY, AA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (17) :6528-6532