A sensitive transcriptome analysis method that can detect unknown transcripts

被引:73
作者
Fukumura, R
Takahashi, H
Saito, T
Tsutsumi, Y
Fujimori, A
Sato, S
Tatsumi, K
Araki, R
Abe, M
机构
[1] Natl Inst Radiol Sci, Transcriptome Profiling Grp, Inage Ku, Chiba 2638555, Japan
[2] Japan Soc Promot Sci Domest Res Fellowship, Chiyoda Ku, Tokyo 1028471, Japan
[3] Maze Inc, Shibuya Ku, Tokyo 1510072, Japan
关键词
D O I
10.1093/nar/gng094
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
We have developed an AFLP-based gene expression profiling method called 'high coverage expression profiling' (HiCEP) analysis. By making improvements to the selective PCR technique we have reduced the rate of false positive peaks to similar to4% and consequently the number of peaks, including overlapping peaks, has been markedly decreased. As a result we can determine the relationship between peaks and original transcripts unequivocally. This will make it practical to prepare a database of all peaks, allowing gene assignment without having to isolate individual peaks. This precise selection also enables us to easily clone peaks of interest and predict the corresponding gene for each peak in some species. The procedure is highly reproducible and sensitive enough to detect even a 1.2-fold difference in gene expression. Most importantly, the low false positive rate enables us to analyze gene expression with wide coverage by means of four instead of six nucleotide recognition site restriction enzymes for fingerprinting mRNAs. Therefore, the method detects 70-80% of all transcripts, including non-coding transcripts, unknown and known genes. Moreover, the method requires no sequence information and so is applicable even to eukaryotes for which there is no genome information available.
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页数:7
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共 19 条
[1]   Options available - from start to finish - for obtaining expression data by microarray [J].
Bowtell, DDL .
NATURE GENETICS, 1999, 21 (Suppl 1) :25-32
[2]   A genome-wide transcriptional analysis of the mitotic cell cycle [J].
Cho, RJ ;
Campbell, MJ ;
Winzeler, EA ;
Steinmetz, L ;
Conway, A ;
Wodicka, L ;
Wolfsberg, TG ;
Gabrielian, AE ;
Landsman, D ;
Lockhart, DJ ;
Davis, RW .
MOLECULAR CELL, 1998, 2 (01) :65-73
[3]   Non-coding RNA genes and the modern RNA world [J].
Eddy, SR .
NATURE REVIEWS GENETICS, 2001, 2 (12) :919-929
[4]   Open systems: panoramic views of gene expression [J].
Green, CD ;
Simons, JF ;
Taillon, BE ;
Lewin, DA .
JOURNAL OF IMMUNOLOGICAL METHODS, 2001, 250 (1-2) :67-79
[5]  
Kato K, 1997, Tanpakushitsu Kakusan Koso, V42, P2876
[6]   DESCRIPTION OF THE ENTIRE MESSENGER-RNA POPULATION BY A 3'-END CDNA FRAGMENT GENERATED BY CLASS IIS RESTRICTION ENZYMES [J].
KATO, K .
NUCLEIC ACIDS RESEARCH, 1995, 23 (18) :3685-3690
[7]   Sequencing and comparison of yeast species to identify genes and regulatory elements [J].
Kellis, M ;
Patterson, N ;
Endrizzi, M ;
Birren, B ;
Lander, ES .
NATURE, 2003, 423 (6937) :241-254
[8]   A novel method using edge detection for signal extraction from cDNA microarray image analysis [J].
Kim, JH ;
Kim, HY ;
Lee, YS .
EXPERIMENTAL AND MOLECULAR MEDICINE, 2001, 33 (02) :83-88
[9]  
Kurian KM, 1999, J PATHOL, V187, P267
[10]   DIFFERENTIAL DISPLAY OF EUKARYOTIC MESSENGER-RNA BY MEANS OF THE POLYMERASE CHAIN-REACTION [J].
LIANG, P ;
PARDEE, AB .
SCIENCE, 1992, 257 (5072) :967-971