Genome-wide estimation of transcript concentrations from spotted cDNA microarray data

被引:17
作者
Frigessi, A
van de Wiel, MA
Holden, M
Svendsrud, DH
Glad, IK
Lyng, H
机构
[1] Univ Oslo, Dept Biostat, Inst Basic Med Sci, N-0317 Oslo, Norway
[2] Univ Oslo, Dept Math, N-0317 Oslo, Norway
[3] Norwegian Comp Ctr, Oslo, Norway
[4] Tech Univ Eindhoven, Dept Math & Comp Sci, NL-5600 MB Eindhoven, Netherlands
[5] Norwegian Radium Hosp, Hlth Enterprise Rikshosp, Dept Radiat Biol, Oslo, Norway
关键词
D O I
10.1093/nar/gni141
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 method providing absolute transcript concentrations from spotted microarray intensity data is presented. Number of transcripts per mu g total RNA, mRNA or per cell, are obtained for each gene, enabling comparisons of transcript levels within and between tissues. The method is based on Bayesian statistical modelling incorporating available information about the experiment from target preparation to image analysis, leading to realistically large confidence intervals for estimated concentrations. The method was validated in experiments using transcripts at known concentrations, showing accuracy and reproducibility of estimated concentrations, which were also in excellent agreement with results from quantitative real-time PCR. We determined the concentration for 10 157 genes in cervix cancers and a pool of cancer cell lines and found values in the range of 10(5)-10(10) transcripts per mu g total RNA. The precision of our estimates was sufficiently high to detect significant concentration differences between two tumours and between different genes within the same tumour, comparisons that are not possible with standard intensity ratios. Our method can be used to explore the regulation of pathways and to develop individualized therapies, based on absolute transcript concentrations. It can be applied broadly, facilitating the construction of the transcriptome, continuously updating it by integrating future data.
引用
收藏
页码:1 / 13
页数:13
相关论文
共 36 条
[1]  
Ausubel FM, 2000, CURRENT PROTOCOLS MO, V1
[2]   DEVELOPMENTALLY REGULATED MESSENGER-RNAS IN MOUSE-LIVER [J].
BARTH, RK ;
GROSS, KW ;
GREMKE, LC ;
HASTIE, ND .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1982, 79 (02) :500-504
[3]   The Bayesian revolution in genetics [J].
Beaumont, MA ;
Rannala, B .
NATURE REVIEWS GENETICS, 2004, 5 (04) :251-261
[4]   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
[5]   Exploring the new world of the genome with DNA microarrays [J].
Brown, PO ;
Botstein, D .
NATURE GENETICS, 1999, 21 (Suppl 1) :33-37
[6]   The use and analysis of microarray data [J].
Butte, A .
NATURE REVIEWS DRUG DISCOVERY, 2002, 1 (12) :951-960
[7]   Combining multiple microarray studies and modeling interstudy variation [J].
Choi, Jung Kyoon ;
Yu, Ungsik ;
Kim, Sangsoo ;
Yoo, Ook Joon .
BIOINFORMATICS, 2003, 19 :i84-i90
[8]   Fundamentals of experimental design for cDNA microarrays [J].
Churchill, GA .
NATURE GENETICS, 2002, 32 (Suppl 4) :490-495
[9]   Bayesian estimation of transcript levels using a general model of array measurement noise [J].
Dror, RO ;
Murnick, JG ;
Rinaldi, NJ ;
Marinescu, VD ;
Rifkin, RM ;
Young, RA .
JOURNAL OF COMPUTATIONAL BIOLOGY, 2003, 10 (3-4) :433-452
[10]   Measuring absolute expression with microarrays with a calibrated reference sample and an extended signal intensity range [J].
Dudley, AM ;
Aach, J ;
Steffen, MA ;
Church, GM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (11) :7554-7559