Changes in the transcriptional profile of cardiac myocytes following green fluorescent protein expression

被引:13
作者
Badrian, Bahareh
Bogoyevitch, Marie A. [1 ]
机构
[1] Univ Western Australia, Sch Biomed Biomol & Chem Sci, Perth, WA 6009, Australia
[2] Univ Melbourne, Bio21 Inst, Dept Biochem & Mol Biol, Melbourne, Vic, Australia
关键词
D O I
10.1089/dna.2007.0604
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Green fluorescent protein ( GFP) and its multiple forms, such as enhanced GFP ( EGFP), have been widely used as marker proteins and for tracking purposes in many biological systems, including the heart and cardiac cell systems. Despite some concerns on its toxicity under certain circumstances, GFP remains amongst the most reliable and easy-to-use markers available. Using rat full genome DNA microarrays, we have investigated the broader consequences of adenoviral- driven GFP expression in cardiac myocytes. In our transcriptional profiling analysis, we set a threshold of a twofold change. We removed possible changes resulting from adenoviral infection by comparison with transcriptional profiles of cardiac myocytes with adenoviral- driven expression of an unrelated protein, the kinase MEK. Our analysis revealed changes in the expression of 212 genes. Of these genes, 174 were upregulated and 38 were downregulated following GFP expression. Many of these genes remain unannotated, but an evaluation of those with described functions for their resulting proteins indicated that many were involved in processes, including responses to stimuli/stress and signal transduction. Our analysis thus indicates the broader consequences of GFP expression in altering gene expression profiles in cardiac cells. Care should therefore be taken when using GFP expression as a control in gene expression studies.
引用
收藏
页码:727 / 736
页数:10
相关论文
共 53 条
[1]
RGS proteins have a signalling complex: Interactions between RGS proteins and GPCRs, effectors, and auxiliary proteins [J].
Abramow-Newerly, M ;
Roy, AA ;
Nunn, C ;
Chidiac, P .
CELLULAR SIGNALLING, 2006, 18 (05) :579-591
[2]
GFP expression in muscle cells impairs actin-myosin interactions:: implications for cell therapy [J].
Agbulut, O ;
Coirault, C ;
Niederländer, N ;
Huet, A ;
Vicart, P ;
Hagège, A ;
Puceat, M ;
Menasché, P .
NATURE METHODS, 2006, 3 (05) :331-331
[3]
Green fluorescent protein impairs actin-myosin interactions by binding to the actin-binding site of myosin [J].
Agbulut, Onnik ;
Huet, Alexis ;
Niederlander, Nicolas ;
Puceat, Michel ;
Menasche, Philippe ;
Coirault, Catherine .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (14) :10465-10471
[4]
Altered expression and function of P-glycoprotein (170 kDa), encoded by the MDR 1 gene, in T cell subsets from aging humans [J].
Aggarwal, S ;
Tsuruo, T ;
Gupta, S .
JOURNAL OF CLINICAL IMMUNOLOGY, 1997, 17 (06) :448-454
[5]
AHMED S, 1995, METHOD ENZYMOL, V256, P114
[6]
Allen Matthew, 1994, Clinical Materials, V16, P189
[7]
Interaction between the 2′-5′ oligoadenylate synthetase-like protein p59 OASL and the transcriptional repressor methyl CpG-binding protein 1 [J].
Andersen, JB ;
Strandbygård, DJ ;
Hartmann, R ;
Justesen, J .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 2004, 271 (03) :628-636
[8]
Arun K. H. S., 2005, Journal of Pharmacological and Toxicological Methods, V51, P1, DOI 10.1016/j.vascn.2004.07.006
[9]
Gene expression profiling reveals complex changes following MEK-EE expression in cardiac myocytes [J].
Badrian, Bahareh ;
Bogoyevitch, Marie A. .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2007, 39 (02) :349-365
[10]
Contrasting actions of prolonged mitogen-activated protein kinase activation on cell survival [J].
Badrian, Bahareh ;
Casey, Tammy M. ;
Lai, May C. ;
Rakoczy, P. Elizabeth ;
Arthur, Peter G. ;
Bogoyevitch, Marie A. .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2006, 345 (02) :843-850