MicroSAGE: a modified procedure for serial analysis of gene expression in limited amounts of tissue

被引:117
作者
Datson, NA [1 ]
van der Perk-de Jong, J [1 ]
van den Berg, MP [1 ]
de Kloet, ER [1 ]
Vreugdenhil, E [1 ]
机构
[1] Leiden Univ, Leiden Amsterdam Ctr Drug Res, Div Med Pharmacol, NL-2300 RA Leiden, Netherlands
关键词
D O I
10.1093/nar/27.5.1300
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
Serial Analysis of Gene Expression (SAGE) is a powerful expression profiling method, allowing the analysis of the expression of thousands of transcripts simultaneously, A disadvantage of the method, however, is the relatively high amount of input RNA required. Consequently, SAGE cannot be used for the generation of expression profiles when RNA is limited, i.e. in small biological samples such as tissue biopsies or microdissected material. Here we describe a modification of SAGE, named microSAGE, which requires 500- to 5000-fold less starting material. Compared with SAGE, microSAGE is simplified due to incorporation of a 'single-tube' procedure for all steps from RNA isolation to tag release, Furthermore, a limited number of additional PCR cycles are performed. Using microSAGE gene expression profiles can be obtained from minute quantities of tissue such as a single hippocampal punch from a rat brain slice of 325 mu m thickness, estimated to contain, at most, 10(5) cells. This method opens up a multitude of new possibilities for the application of SAGE, for example the characterization of expression profiles in tissue biopsies, tumor metastases or in other cases where tissue is scarce and the generation of region-specific expression profiles of complex heterogeneous tissues.
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收藏
页码:1300 / 1307
页数:8
相关论文
共 30 条
[1]   3,400 NEW EXPRESSED SEQUENCE TAGS IDENTIFY DIVERSITY OF TRANSCRIPTS IN HUMAN BRAIN [J].
ADAMS, MD ;
KERLAVAGE, AR ;
FIELDS, C ;
VENTER, JC .
NATURE GENETICS, 1993, 4 (03) :256-267
[2]   Serial analysis of gene expression: ESTs get smaller [J].
Adams, MD .
BIOESSAYS, 1996, 18 (04) :261-262
[3]   SEQUENCE IDENTIFICATION OF 2,375 HUMAN BRAIN GENES [J].
ADAMS, MD ;
DUBNICK, M ;
KERLAVAGE, AR ;
MORENO, R ;
KELLEY, JM ;
UTTERBACK, TR ;
NAGLE, JW ;
FIELDS, C ;
VENTER, JC .
NATURE, 1992, 355 (6361) :632-634
[4]   COMPLEMENTARY-DNA SEQUENCING - EXPRESSED SEQUENCE TAGS AND HUMAN GENOME PROJECT [J].
ADAMS, MD ;
KELLEY, JM ;
GOCAYNE, JD ;
DUBNICK, M ;
POLYMEROPOULOS, MH ;
XIAO, H ;
MERRIL, CR ;
WU, A ;
OLDE, B ;
MORENO, RF ;
KERLAVAGE, AR ;
MCCOMBIE, WR ;
VENTER, JC .
SCIENCE, 1991, 252 (5013) :1651-1656
[5]   Analysis of a sequenced cDNA library from multiple sclerosis lesions [J].
Becker, KG ;
Mattson, DH ;
Powers, JM ;
Gado, AM ;
Biddison, WE .
JOURNAL OF NEUROIMMUNOLOGY, 1997, 77 (01) :27-38
[6]   Brain corticosteroid receptor balance in health and disease [J].
De Kloet, ER ;
Vreugdenhil, E ;
Oitzl, MS ;
Joëls, M .
ENDOCRINE REVIEWS, 1998, 19 (03) :269-301
[7]  
DREWE JA, 1992, J NEUROSCI, V12, P538
[8]  
Francia G, 1996, CANCER RES, V56, P3855
[9]   Developmentally regulated gene expression of all eight metabotropic glutamate receptors in hypothalamic suprachiasmatic and arcuate nuclei - a PCR analysis [J].
Ghosh, PK ;
Baskaran, N ;
vandenPol, AN .
DEVELOPMENTAL BRAIN RESEARCH, 1997, 102 (01) :1-12
[10]  
Lanahan A, 1997, J NEUROSCI, V17, P2876