Gene expression analysis for high throughput screening applications

被引:0
作者
Pinhasov, A [1 ]
Mei, J [1 ]
Amaratunga, D [1 ]
Amato, FA [1 ]
Lu, H [1 ]
Kauffman, J [1 ]
Xin, H [1 ]
Brenneman, DE [1 ]
Johnson, DL [1 ]
Andrade-Gordon, P [1 ]
Ilyin, SE [1 ]
机构
[1] Johnson & Johnson Pharmaceut Res & Dev LLC, Spring House, PA 19477 USA
关键词
TaqMan; Allegro; RT-PCR; gene expression; cytokines; drug discovery; neurodegenerative diseases; cancer;
D O I
暂无
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
To meet growing needs for high throughput gene expression profiling, we established a new automated high throughput TaqMan RT-PCR method for quantitative mRNA expression analysis. In this method, the Allegro(TM) (Zymark) system conducts all sample tracking and liquid handling steps, and ABI PRISM(R) 7900 HT (Applied Biosystems) is used to conduct real-time determination of the C-t value when amplification of PCR products is first detected and accumulation of inhibitory PCR products is unlikely to occur. The ABI PRISM(R) 7900 HT Sequence Detection System features a real-time PCR instrument with 384-well-plate compatibility and robotic loading, and continuous wavelength detection, which enables the use of multiple fluorophores in a single reaction. The Allegro System offers an assembly line approach with a modular design that allows reconfiguration of the components to accommodate variations in the assay flow. In the present study, we have established and validated a new automated High Throughput (FIT) TaqMan RT-PCR-based method for quantitative mRNA expression analysis. The data demonstrate that HT-Taqman PCR is a powerful tool that can be used for measuring low concentrations of mRNA, and is highly accurate, reproducible, and amenable to high throughput analysis. Results suggest that HT-TaqMan is a reliable method for the quantification of low-expression genes and a powerful tool with FIT capability for target identification/validation, structure-activity relationship (SAR) study, compound selection for efficacy studies, and biomarker identification in drug discovery and development.
引用
收藏
页码:133 / 140
页数:8
相关论文
共 23 条
  • [1] DNA arrays and neurobiollogy - what's new and what's next?
    Barlow, C
    Lockhart, DJ
    [J]. CURRENT OPINION IN NEUROBIOLOGY, 2002, 12 (05) : 554 - 561
  • [2] Transforming growth factor β1 prevents IL-1β-induced microglial activation, whereas TNFα- and IL-6-stimulated activation are not antagonized
    Basu, A
    Krady, JK
    Enterline, JR
    Levison, SW
    [J]. GLIA, 2002, 40 (01) : 109 - 120
  • [3] CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
  • [4] DeRisi J, 1996, NAT GENET, V14, P457
  • [5] ANALYSIS OF CYTOKINE MESSENGER-RNA AND DNA - DETECTION AND QUANTITATION BY COMPETITIVE POLYMERASE CHAIN-REACTION
    GILLILAND, G
    PERRIN, S
    BLANCHARD, K
    BUNN, HF
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (07) : 2725 - 2729
  • [6] Real time quantitative PCR
    Heid, CA
    Stevens, J
    Livak, KJ
    Williams, PM
    [J]. GENOME RESEARCH, 1996, 6 (10): : 986 - 994
  • [7] Brain tumor development in rats is associated with changes in central nervous system cytokine and neuropeptide systems
    Ilyin, SE
    Gayle, D
    González-Gómez, I
    Miele, ME
    Plata-Salamán, CR
    [J]. BRAIN RESEARCH BULLETIN, 1999, 48 (04) : 363 - 373
  • [8] Modifications of RNase protection assay for neuroscience applications
    Ilyin, SE
    Gayle, D
    Plata-Salamán, CR
    [J]. JOURNAL OF NEUROSCIENCE METHODS, 1998, 84 (1-2) : 139 - 141
  • [9] Reliability of reverse transcription-polymerase chain reaction (RT-PCR)-based assays for the detection of circulating tumour cells:: A quality-assurance initiative of the EORTC melanoma cooperative group
    Keilholz, U
    Willhauck, M
    Rimoldi, D
    Brasseur, F
    Dummer, W
    Rass, K
    de Vries, T
    Blaheta, J
    Voit, C
    Lethé, B
    Burchill, S
    [J]. EUROPEAN JOURNAL OF CANCER, 1998, 34 (05) : 750 - 753
  • [10] A rapid method for semiquantitative analysis of the human V beta-repertoire using TaqMan(R) PCR
    Lang, R
    Pfeffer, K
    Wagner, H
    Heeg, K
    [J]. JOURNAL OF IMMUNOLOGICAL METHODS, 1997, 203 (02) : 181 - 192