Systems Biology of Interferon Responses

被引:92
作者
Hertzog, Paul [1 ]
Forster, Sam [1 ]
Samarajiwa, Shamith [1 ]
机构
[1] Monash Univ, Monash Inst Med Res, Ctr Innate Immun & Infect Dis, Clayton, Vic 3168, Australia
基金
英国医学研究理事会;
关键词
RECEPTORS; GENES; MOUSE;
D O I
10.1089/jir.2010.0126
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The interferons (IFNs) are a pleiotropic family of cytokines that perform fundamental functions in protecting host organisms from disease and in maintaining homeostasis. Like other multifunctional cytokines, excessive or inappropriate activity can cause toxicity and even death. Therefore, host organisms have evolved specific and highly regulated mechanisms to control the temporal and tissue specificity of production of IFNs and the selection of pathways and genes to be activated as the effectors of the IFN response in cells. There are now numerous microarray datasets available to enable a "global" analysis of the genes involved in the IFN response. This article describes the INTERFEROME database, which assimilates the available expression profiling data and its contents and enables the definition of IFN-regulated genes, discovery of pathways, regulatory networks, and tissue specificities of the IFN response.
引用
收藏
页码:5 / 11
页数:7
相关论文
共 34 条
[1]   Gene Ontology: tool for the unification of biology [J].
Ashburner, M ;
Ball, CA ;
Blake, JA ;
Botstein, D ;
Butler, H ;
Cherry, JM ;
Davis, AP ;
Dolinski, K ;
Dwight, SS ;
Eppig, JT ;
Harris, MA ;
Hill, DP ;
Issel-Tarver, L ;
Kasarskis, A ;
Lewis, S ;
Matese, JC ;
Richardson, JE ;
Ringwald, M ;
Rubin, GM ;
Sherlock, G .
NATURE GENETICS, 2000, 25 (01) :25-29
[2]   Nucleic acids of mammalian origin can act as endogenous ligands for toll-like receptors and may promote systemic lupus erythematosus [J].
Barrat, FJ ;
Meeker, T ;
Gregorio, J ;
Chan, JH ;
Uematsu, S ;
Akira, S ;
Chang, B ;
Duramad, O ;
Coffman, RL .
JOURNAL OF EXPERIMENTAL MEDICINE, 2005, 202 (08) :1131-1139
[3]  
CHAKRABARTI A, 2010, J INTERFERON CYTOKIN, V31, P49
[4]   Combination therapy in multiple sclerosis [J].
Conway, Devon ;
Cohen, Jeffrey A. .
LANCET NEUROLOGY, 2010, 9 (03) :299-308
[5]   Type I interferon receptors: Biochemistry and biological functions [J].
de Weerd, Nicole A. ;
Samarajiwa, Shamith A. ;
Hertzog, Paul J. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (28) :20053-20057
[6]   JAKs and STATs in invertebrate model organisms [J].
Dearolf, CR .
CELLULAR AND MOLECULAR LIFE SCIENCES, 1999, 55 (12) :1578-1584
[7]  
Fitzgerald KA, 2010, J INTERFERON CYTOKIN, V31, P131
[8]   Functional Crosstalk between Type I and II Interferon through the Regulated Expression of STAT1 [J].
Gough, Daniel J. ;
Messina, Nicole L. ;
Hii, Linda ;
Gould, Jodee A. ;
Sabapathy, Kanaga ;
Robertson, Ashley P. S. ;
Trapani, Joseph A. ;
Levy, David E. ;
Hertzog, Paul J. ;
Clarke, Christopher J. P. ;
Johnstone, Ricky W. .
PLOS BIOLOGY, 2010, 8 (04)
[9]   Review of recent genome-wide association scans in lupus [J].
Graham, R. R. ;
Hom, G. ;
Ortmann, W. ;
Behrens, T. W. .
JOURNAL OF INTERNAL MEDICINE, 2009, 265 (06) :680-688
[10]   Human MxA Protein: An Interferon-Induced Dynamin-Like GTPase with Broad Antiviral Activity [J].
Haller, Otto ;
Kochs, Georg .
JOURNAL OF INTERFERON AND CYTOKINE RESEARCH, 2011, 31 (01) :79-87