Expression profiling methods used in drug abuse research

被引:13
作者
Gebicke-Haerter, PJ [1 ]
机构
[1] Heidelberg Univ, Cent Inst Mental Hlth, Dept Psychopharmacol, D-68159 Mannheim, Germany
关键词
D O I
10.1080/13556210412331327812
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
A variety of analytical methodologies to investigate gene expression patterns in cells or tissues have been developed. For screennig purposes, a large number of target mRNAs have to be interrogated simultaneously. These requirements have been met more or less comprehensively by Differential Display (DD) RT-PCR, Suppression Subtractive Hybridization (SSH), Serial Analysis of Gene Expression (SAGE), and DNA chips. The ultimate goal to cover any gene transcript potentially gene expressed by a given cell is on the way to be achieved by microbead arrays and by Affymetrix chips. Once targets of interest are identified, techniques employing low degrees of multiplexing, such as RNAse protection assays or some bead-based techniques (Luminex) eventually provide extremely fast results on the diagnostic level. With the aid of powerful computer programs, expression profiling technologies have opened intriguing new insights into the complex world of gene regulation. These new techniques have also been applied in drug abuse research recently and some examples of such approaches are described.
引用
收藏
页码:37 / 46
页数:10
相关论文
共 79 条
[1]   Microarray analysis of genes expressed in the frontal cortex of rats chronically treated with morphine and after naloxone precipitated withdrawal [J].
Ammon, S ;
Mayer, P ;
Riechert, U ;
Tischmeyer, H ;
Höllt, V .
MOLECULAR BRAIN RESEARCH, 2003, 112 (1-2) :113-125
[2]   Morphine-induced changes of gene expression in the brain [J].
Ammon-Treiber, S ;
Höllt, V .
ADDICTION BIOLOGY, 2005, 10 (01) :81-89
[3]   Altered inhibitory input to Purkinje cells of dystrophin-deficient mice [J].
Anderson, JL ;
Head, SI ;
Morley, JW .
BRAIN RESEARCH, 2003, 982 (02) :280-283
[4]   Discrete cell gene profiling of ventral tegmental dopamine neurons after acute and chronic cocaine self-administration [J].
Backes, E ;
Hemby, SE .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2003, 307 (02) :450-459
[5]   CD81-induced behavioural changes during chronic cocaine administration:: in vivo gene delivery with regulatable lentivirus [J].
Bahi, A ;
Boyer, F ;
Kafri, T ;
Dreyer, JL .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2004, 19 (06) :1621-1633
[6]   Issues for consideration in the analysis of microarray data in behavioural studies [J].
Barr, GA ;
Gao, PH .
ADDICTION BIOLOGY, 2005, 10 (01) :15-21
[7]   Effects of chronic exposure to cocaine are regulated by the neuronal protein Cdk5 [J].
Bibb, JA ;
Chen, JS ;
Taylor, JR ;
Svenningsson, P ;
Nishi, A ;
Snyder, GL ;
Yan, Z ;
Sagawa, ZK ;
Ouimet, CC ;
Nairn, AC ;
Nestler, EJ ;
Greengard, P .
NATURE, 2001, 410 (6826) :376-380
[8]   Options available - from start to finish - for obtaining expression data by microarray [J].
Bowtell, DDL .
NATURE GENETICS, 1999, 21 (Suppl 1) :25-32
[9]   In vitro cloning of complex mixtures of DNA on microbeads:: Physical separation of differentially expressed cDNAs [J].
Brenner, S ;
Williams, SR ;
Vermaas, EH ;
Storck, T ;
Moon, K ;
McCollum, C ;
Mao, JI ;
Luo, SJ ;
Kirchner, JJ ;
Eletr, S ;
DuBridge, RB ;
Burcham, T ;
Albrecht, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (04) :1665-1670
[10]   Gene expression analysis by massively parallel signature sequencing (MPSS) on microbead arrays [J].
Brenner, S ;
Johnson, M ;
Bridgham, J ;
Golda, G ;
Lloyd, DH ;
Johnson, D ;
Luo, SJ ;
McCurdy, S ;
Foy, M ;
Ewan, M ;
Roth, R ;
George, D ;
Eletr, S ;
Albrecht, G ;
Vermaas, E ;
Williams, SR ;
Moon, K ;
Burcham, T ;
Pallas, M ;
DuBridge, RB ;
Kirchner, J ;
Fearon, K ;
Mao, J ;
Corcoran, K .
NATURE BIOTECHNOLOGY, 2000, 18 (06) :630-634