High-throughput gene expression analysis for drug discovery

被引:34
作者
Lennon, GG [1 ]
机构
[1] Gene Log, Gaithersburg, MD 20878 USA
关键词
D O I
10.1016/S1359-6446(99)01448-8
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The ability to rapidly survey and compare gene expression levels between reference and test samples is moving the drug discovery process towards a more genomic orientation. The success of the Human Genome Project and related private genomics initiatives, combined with new technologies to probe, image and access expression data, are responsible for this transformation. This article reviews the history, status and future direction of high-throughput gene expression analysis. It describes classical approaches, explains the development of methods such as differential display for discovering novel genes, and discusses how microarray technology is exploiting collections of known sequences to pinpoint drug targets.
引用
收藏
页码:59 / 66
页数:8
相关论文
共 32 条
[1]   METHOD FOR DETECTION OF SPECIFIC RNAS IN AGAROSE GELS BY TRANSFER TO DIAZOBENZYLOXYMETHYL-PAPER AND HYBRIDIZATION WITH DNA PROBES [J].
ALWINE, JC ;
KEMP, DJ ;
STARK, GR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1977, 74 (12) :5350-5354
[2]  
BEECHER JE, 1997, POLYM MAT SCI ENG, V76, P597
[3]   SIZING AND MAPPING OF EARLY ADENOVIRUS MESSENGER-RNAS BY GEL-ELECTROPHORESIS OF S1 ENDONUCLEASE-DIGESTED HYBRIDS [J].
BERK, AJ ;
SHARP, PA .
CELL, 1977, 12 (03) :721-732
[4]  
BOWELL DL, 1999, NAT GENET S, V21, P25
[5]   The integration of microarray information in the drug development process [J].
Braxton, S ;
Bedilion, T .
CURRENT OPINION IN BIOTECHNOLOGY, 1998, 9 (06) :643-649
[6]   Suppression subtractive hybridization: A method for generating differentially regulated or tissue-specific cDNA probes and libraries [J].
Diatchenko, L ;
Lau, YFC ;
Campbell, AP ;
Chenchik, A ;
Moqadam, F ;
Huang, B ;
Lukyanov, S ;
Lukyanov, K ;
Gurskaya, N ;
Sverdlov, ED ;
Siebert, PD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (12) :6025-6030
[7]   Exploiting chemical libraries, structure, and genomics in the search for kinase inhibitors [J].
Gray, NS ;
Wodicka, L ;
Thunnissen, AMWH ;
Norman, TC ;
Kwon, SJ ;
Espinoza, FH ;
Morgan, DO ;
Barnes, G ;
LeClerc, S ;
Meijer, L ;
Kim, SH ;
Lockhart, DJ ;
Schultz, PG .
SCIENCE, 1998, 281 (5376) :533-538
[8]   STIMULATION OF 3T3 CELLS INDUCES TRANSCRIPTION OF THE C-FOS PROTO-ONCOGENE [J].
GREENBERG, ME ;
ZIFF, EB .
NATURE, 1984, 311 (5985) :433-438
[9]   HYBRIDIZATION FINGERPRINTING OF HIGH-DENSITY CDNA-LIBRARY ARRAYS WITH CDNA POOLS DERIVED FROM WHOLE TISSUES [J].
GRESS, TM ;
HOHEISEL, JD ;
LENNON, GG ;
ZEHETNER, G ;
LEHRACH, H .
MAMMALIAN GENOME, 1992, 3 (11) :609-619
[10]   ISOLATION OF CDNA CLONES ENCODING T-CELL-SPECIFIC MEMBRANE-ASSOCIATED PROTEINS [J].
HEDRICK, SM ;
COHEN, DI ;
NIELSEN, EA ;
DAVIS, MM .
NATURE, 1984, 308 (5955) :149-153