Differential gene expression patterns revealed by oligonucleotide versus long cDNA arrays

被引:97
作者
Li, J
Pankratz, M
Johnson, JA
机构
[1] Univ Wisconsin, Weisman Ctr, Madison, WI 53705 USA
[2] Univ Wisconsin, Sch Pharm, Madison, WI 53705 USA
[3] Univ Wisconsin, Mol & Environm Toxicol Ctr, Madison, WI 53705 USA
[4] Univ Wisconsin, Ctr Neurosci, Madison, WI 53705 USA
关键词
DNA arrays; gene expression; antioxidant responsive element; cross-hybridization; tert-butylhydroquinone;
D O I
10.1093/toxsci/69.2.383
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
DNA microarrays can be classified into oligonucleotides (Affymetrix) or long cDNAs (IncyteGenomics) based on the arrayed probes. Unfortunately, data are lacking on the comparison of these two popular global screening array systems. The present study was designed to assess the reliability of datasets generated by the two platforms from the same samples. We have already established a model for upregulation of a cluster of antioxidant responsive element (ARE)-driven genes in a human neuroblastoma cell line by treatment with tert-butylhydroquinone (tBHQ) for 8 and 24 h. HuGene FL (Affymetrix), U95 Av2 (Affymetrix), and UniGem V 2.0 (IncyteGenomics) were chosen to do the comparative study on 8- and 24-h samples. The Affymetrix data generated from U95Av2 chips demonstrated that the mRNA of 218 (2.3% of total clones) genes was increased after 8 h of tBHQ treatment. This list included most of the known ARE-driven genes, and nine selected genes showed a high consistency with RT-PCR results. IncyteGenomics called four genes increased and no genes were decreased. These same four genes were also called by the Affymetrix microarray. The sensitivity (fluorescence intensity) and specificity (fold) were very different for selected genes when comparing the two platforms. Cross-hybridization was shown to partially contribute to the discrepancies of the data generated by the two platforms. According to our results, the data generated from oligonucleotide microarrays is more reliable for interrogating changes in gene expression than data from long cDNA microarrays.
引用
收藏
页码:383 / 390
页数:8
相关论文
共 23 条
[1]   Development of a toxicological gene array and quantitative assessment of this technology [J].
Bartosiewicz, M ;
Trounstine, M ;
Barker, D ;
Johnston, R ;
Buckpitt, A .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2000, 376 (01) :66-73
[2]   Hybridization cross-reactivity within homologous gene families on glass cDNA microarrays [J].
Evertsz, EM ;
Au-Young, J ;
Ruvolo, MV ;
Lim, AC ;
Reynolds, MA .
BIOTECHNIQUES, 2001, 31 (05) :1182-+
[3]   Monitoring gene expression using DNA microarrays [J].
Harrington, CA ;
Rosenow, C ;
Retief, J .
CURRENT OPINION IN MICROBIOLOGY, 2000, 3 (03) :285-291
[4]   Molecular basis for the contribution of the antioxidant responsive element to cancer chemoprevention [J].
Hayes, JD ;
McMahon, M .
CANCER LETTERS, 2001, 174 (02) :103-113
[5]   Discovery and analysis of inflammatory disease-related genes using cDNA microarrays [J].
Heller, RA ;
Schena, M ;
Chai, A ;
Shalon, D ;
Bedilion, T ;
Gilmore, J ;
Woolley, DE ;
Davis, RW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (06) :2150-2155
[6]   Regulatory mechanisms of cellular response to oxidative stress [J].
Itoh, K ;
Ishii, T ;
Wakabayashi, N ;
Yamamoto, M .
FREE RADICAL RESEARCH, 1999, 31 (04) :319-324
[7]   Regulation of genes encoding NAD(P)H:quinone oxidoreductases [J].
Jaiswal, AK .
FREE RADICAL BIOLOGY AND MEDICINE, 2000, 29 (3-4) :254-262
[8]   Assessment of the sensitivity and specificity of oligonucleotide (50mer) microarrays [J].
Kane, MD ;
Jatkoe, TA ;
Stumpf, CR ;
Lu, J ;
Thomas, JD ;
Madore, SJ .
NUCLEIC ACIDS RESEARCH, 2000, 28 (22) :4552-4557
[9]   Nrf2-dependent activation of the antioxidant responsive element by tert-butylhydroquinone is independent of oxidative stress in IMR-32 human neuroblastoma cells [J].
Lee, JM ;
Moehlenkamp, JD ;
Hanson, JM ;
Johnson, JA .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2001, 280 (01) :286-292
[10]   Phosphatidylinositol 3-kinase, not extracellular signal-regulated kinase, regulates activation of the antioxidant-responsive element in IMR-32 human neuroblastoma cells [J].
Lee, JM ;
Hanson, JM ;
Chu, WA ;
Johnson, JA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (23) :20011-20016