Impact of RNA extraction from limited samples on microarray results

被引:16
作者
Ojaniemi, H
Evengard, B
Lee, DR
Unger, ER
Vernon, SD
机构
[1] Ctr Dis Control & Prevent, Atlanta, GA 30333 USA
[2] Huddinge Univ Hosp, Karolinska Inst, Stockholm, Sweden
[3] Royal Inst Technol, Stockholm, Sweden
关键词
D O I
10.2144/03355st04
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
To move microarray technology into the diagnostic realm, the impact of technical parameters, such as sample preparation and RNA extraction, needs to be understood and minimized. We evaluated the impact of two RNA extraction methods, DNase treatment and the amount of hybridized cDNA probe, on the outcome of microarray results. The results for both RNA extraction methods were comparable, although one method resulted in residual DNA that slightly affected the microarray results. As little as one microgram of total RNA could be used to synthesize a cDNA probe and resulted in a gene expression profile that was similar to one produced using 5 mug total RNA, even though the overall signal intensity was lower. These experiments illustrate that microarray technology holds great promise for the use of limited clinical samples in the diagnostic setting.
引用
收藏
页码:968 / 973
页数:6
相关论文
共 11 条
[1]  
[Anonymous], [No title captured]
[2]   High-sensitivity detection of DNA hybridization on microarrays using resonance light scattering [J].
Bao, P ;
Frutos, AG ;
Greef, C ;
Lahiri, J ;
Muller, U ;
Peterson, TC ;
Warden, L ;
Xie, XY .
ANALYTICAL CHEMISTRY, 2002, 74 (08) :1792-1797
[3]   Assessment of normal variability in peripheral blood gene expression [J].
Campbell, C ;
Vernon, SD ;
Karem, KL ;
Nisenbaum, R ;
Unger, ER .
DISEASE MARKERS, 2002, 18 (04) :201-206
[4]   Analysis of microarray data using Z score transformation [J].
Cheadle, C ;
Vawter, MP ;
Freed, WJ ;
Becker, KG .
JOURNAL OF MOLECULAR DIAGNOSTICS, 2003, 5 (02) :73-81
[5]   SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION [J].
CHOMCZYNSKI, P ;
SACCHI, N .
ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) :156-159
[6]   THE PREPARATION OF POLY(A)+MESSENGER RNA FROM THE HAGFISH SLIME GLAND [J].
GADBOIS, DM ;
SALO, WL ;
ANN, DK ;
DOWNING, SW ;
CARLSON, DM .
PREPARATIVE BIOCHEMISTRY, 1988, 18 (01) :67-76
[7]   RNA amplification results in reproducible microarray data with slight ratio bias [J].
Puskás, LG ;
Zvara, A ;
Hackler, L ;
Van Hummelen, P .
BIOTECHNIQUES, 2002, 32 (06) :1330-+
[8]   Use of real-time quantitative PCR to validate the results of cDNA array and differential display PCR technologies [J].
Rajeevan, MS ;
Ranamukhaarachchi, DG ;
Vernon, SD ;
Unger, ER .
METHODS, 2001, 25 (04) :443-451
[9]   Reproducibility of alternative probe synthesis approaches for gene expression profiling with arrays [J].
Vernon, SD ;
Unger, ER ;
Rajeevan, M ;
Dimulescu, IM ;
Nisenbaum, R ;
Campbell, CE .
JOURNAL OF MOLECULAR DIAGNOSTICS, 2000, 2 (03) :124-127
[10]   Utility of the blood for gene expression profiling and biomarker discovery in chronic fatigue syndrome [J].
Vernon, SD ;
Unger, ER ;
Dimulescu, IM ;
Rajeevan, M ;
Reeves, WC .
DISEASE MARKERS, 2002, 18 (04) :193-199