Butyrate induces profound changes in gene expression related to multiple signal pathways in bovine kidney epithelial cells

被引:87
作者
Li, Robert W. [1 ]
Li, CongJun
机构
[1] USDA ARS, Bovine Funct Genom Lab, Anim & Nat Resources Inst, Beltsville, MD 20705 USA
[2] USDA ARS, Growth Biol Lab, Anim & Nat Resources Inst, Beltsville, MD 20705 USA
关键词
D O I
10.1186/1471-2164-7-234
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
Background: Global gene expression profiles of bovine kidney epithelial cells regulated by sodium butyrate were investigated with high-density oligonucleotide microarrays. The bovine microarray with 86,191 distinct 60mer oligonucleotides, each with 4 replicates, was designed and produced with Maskless Array Synthesizer technology. These oligonucleotides represent approximately 45,383 unique cattle sequences. Results: 450 genes significantly regulated by butyrate with a median False Discovery Rate ( FDR) = 0 % were identified. The majority of these genes were repressed by butyrate and associated with cell cycle control. The expression levels of 30 selected genes identified by the microarray were confirmed using real-time PCR. The results from real-time PCR positively correlated ( R = 0.867) with the results from the microarray. Conclusion: This study presented the genes related to multiple signal pathways such as cell cycle control and apoptosis. The profound changes in gene expression elucidate the molecular basis for the pleiotropic effects of butyrate on biological processes. These findings enable better recognition of the full range of beneficial roles butyrate may play during cattle energy metabolism, cell growth and proliferation, and possibly in fighting gastrointestinal pathogens.
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页数:14
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共 53 条
[1]   Butyrate and glucose metabolism by colonocytes in experimental colitis in mice [J].
Ahmad, MS ;
Krishnan, S ;
Ramakrishna, BS ;
Mathan, M ;
Pulimood, AB ;
Murthy, SN .
GUT, 2000, 46 (04) :493-499
[2]   Differential effects of trichostatin A on gelatinase A expression in 3T3 fibroblasts and HT-1080 fibrosarcoma cells: implications for use of TSA in cancer therapy [J].
Ailenberg, M ;
Silverman, M .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 302 (02) :181-185
[3]   In vitro cytoreductive effects on multiple myeloma cells induced by bisphosphonates [J].
Aparicio, A ;
Gardner, A ;
Tu, Y ;
Savage, A ;
Berenson, J ;
Lichtenstein, A .
LEUKEMIA, 1998, 12 (02) :220-229
[4]   Identification and comparative analysis of human colonocyte short-chain fatty acid response genes [J].
Basson, MD ;
Liu, YW ;
Hanly, AM ;
Emenaker, NJ ;
Shenoy, SG ;
Rothberg, BEG .
JOURNAL OF GASTROINTESTINAL SURGERY, 2000, 4 (05) :501-512
[5]   RADIOIMMUNOASSAY OF INSULIN-LIKE GROWTH FACTOR-BINDING PROTEIN-6 IN HUMAN SERUM AND OTHER BODY-FLUIDS [J].
BAXTER, RC ;
SAUNDERS, H .
JOURNAL OF ENDOCRINOLOGY, 1992, 134 (01) :133-139
[6]   Class II histone deacetylases: Structure, function, and regulation [J].
Bertos, NR ;
Wang, AH ;
Yang, XJ .
BIOCHEMISTRY AND CELL BIOLOGY, 2001, 79 (03) :243-252
[7]   A comparison of normalization methods for high density oligonucleotide array data based on variance and bias [J].
Bolstad, BM ;
Irizarry, RA ;
Åstrand, M ;
Speed, TP .
BIOINFORMATICS, 2003, 19 (02) :185-193
[8]   BUTYRATE BLOCKS THE ACCUMULATION OF CDC2 MESSENGER-RNA IN LATE G1 PHASE BUT INHIBITS BOTH THE EARLY AND LATE G1 PROGRESSION IN CHEMICALLY TRANSFORMED MOUSE FIBROBLASTS BP-A31 [J].
CHAROLLAIS, RH ;
BUQUET, C ;
MESTER, J .
JOURNAL OF CELLULAR PHYSIOLOGY, 1990, 145 (01) :46-52
[9]   Short-Chain Fatty Acid Inhibitors of Histone Deacetylases: Promising Anticancer Therapeutics? [J].
Chen, James S. ;
Faller, Douglas V. ;
Spanjaard, Remco A. .
CURRENT CANCER DRUG TARGETS, 2003, 3 (03) :219-236
[10]   Cell growth inhibition and gene expression induced by the histone deacetylase inhibitor, trichostatin A, on human hepatoma cells [J].
Chiba, T ;
Yokosuka, O ;
Fukai, K ;
Kojima, H ;
Tada, M ;
Arai, M ;
Imazeki, F ;
Saisho, H .
ONCOLOGY, 2004, 66 (06) :481-491