Expression imbalance map: a new visualization method for detection of mRNA expression imbalance regions

被引:25
作者
Kano, M
Nishimura, K
Ishikawa, S
Tsutsumi, S
Hirota, K
Hirose, M
Aburatani, H
机构
[1] Univ Tokyo, Sch Engn, Tokyo 1138655, Japan
[2] Univ Tokyo, Sch Informat Sci & Technol, Tokyo 1138655, Japan
[3] Univ Tokyo, Adv Sci & Technol Res Ctr, Dept Informat Syst, Tokyo 1538904, Japan
[4] Univ Tokyo, Genome Sci Div, Tokyo 1538904, Japan
关键词
gene expression profiling; allelic imbalance; chromosome mapping; hypergeometric distribution; computing methodologies;
D O I
10.1152/physiolgenomics.00116.2002
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
We describe the development of a new visualization method, called the expression imbalance map (EIM), for detecting mRNA expression imbalance regions, reflecting genomic losses and gains at a much higher resolution than conventional technologies such as comparative genomic hybridization (CGH). Simple spatial mapping of the microarray expression profiles on chromosomal location provides little information about genomic structure, because mRNA expression levels do not completely reflect genomic copy number and some microarray probes would be of low quality. The EIM, which does not employ arbitrary selection of thresholds in conjunction with hypergeometric distribution-based algorithm, has a high tolerance of these complex factors. The EIM could detect regionally underexpressed or overexpressed genes (called, here, an expression imbalance region) in lung cancer specimens from their gene expression data of oligonucleotide microarray. Many known as well as potential loci with frequent genomic losses or gains were detected as expression imbalance regions by the EIM. Therefore, the EIM should provide the user with further insight into genomic structure through mRNA expression.
引用
收藏
页码:31 / 46
页数:16
相关论文
共 12 条
[1]  
[Anonymous], 2002, PROBABILITY STAT ENG
[2]   Classification of human lung carcinomas by mRNA expression profiling reveals distinct adenocarcinoma subclasses [J].
Bhattacharjee, A ;
Richards, WG ;
Staunton, J ;
Li, C ;
Monti, S ;
Vasa, P ;
Ladd, C ;
Beheshti, J ;
Bueno, R ;
Gillette, M ;
Loda, M ;
Weber, G ;
Mark, EJ ;
Lander, ES ;
Wong, W ;
Johnson, BE ;
Golub, TR ;
Sugarbaker, DJ ;
Meyerson, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (24) :13790-13795
[3]   Cell sampling - Laser capture microdissection: Molecular analysis of tissue [J].
Bonner, RF ;
EmmertBuck, M ;
Cole, K ;
Pohida, T ;
Chuaqui, R ;
Goldstein, S ;
Liotta, LA .
SCIENCE, 1997, 278 (5342) :1481-&
[4]  
Fujii T, 2002, CANCER RES, V62, P3340
[5]   COMPARATIVE GENOMIC HYBRIDIZATION FOR MOLECULAR CYTOGENETIC ANALYSIS OF SOLID TUMORS [J].
KALLIONIEMI, A ;
KALLIONIEMI, OP ;
SUDAR, D ;
RUTOVITZ, D ;
GRAY, JW ;
WALDMAN, F ;
PINKEL, D .
SCIENCE, 1992, 258 (5083) :818-821
[6]   Chromosome 3 imbalances are the most frequent aberration found in non-small cell lung carcinoma [J].
Lu, YJ ;
Dong, XY ;
Shipley, J ;
Zhang, RG ;
Cheng, SJ .
LUNG CANCER, 1999, 23 (01) :61-66
[7]   Distinction in gene expression profiles of oligodendrogliomas with and without allelic loss of 1p [J].
Mukasa, A ;
Ueki, K ;
Matsumoto, S ;
Tsutsumi, S ;
Nishikawa, R ;
Fujimaki, T ;
Asai, A ;
Kirino, T ;
Aburatani, H .
ONCOGENE, 2002, 21 (25) :3961-3968
[8]   Genomic imbalances in human lung adenocarcinomas and squamous cell carcinomas [J].
Pei, JM ;
Balsara, BR ;
Li, W ;
Litwin, S ;
Gabrielson, E ;
Feder, M ;
Jen, J ;
Testa, JR .
GENES CHROMOSOMES & CANCER, 2001, 31 (03) :282-287
[9]  
Petersen S, 2000, BRIT J CANCER, V82, P65
[10]   Genome-wide analysis of DNA copy-number changes using cDNA microarrays [J].
Pollack, JR ;
Perou, CM ;
Alizadeh, AA ;
Eisen, MB ;
Pergamenschikov, A ;
Williams, CF ;
Jeffrey, SS ;
Botstein, D ;
Brown, PO .
NATURE GENETICS, 1999, 23 (01) :41-46