Quenching of microbial samples for increased reliability of microarray data

被引:46
作者
Pieterse, B
Jellema, RH
van der Werf, MJ
机构
[1] TNO, NL-3700 AJ Zeist, Netherlands
[2] Wageningen Ctr Food Sci, NL-6700 AN Wageningen, Netherlands
关键词
quenching; microbial samples; microarray data;
D O I
10.1016/j.mimet.2005.04.035
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Messenger RNA levels change on a minutes scale due to both degradation and de novo transcription. Consequently, alterations in the transcript profiles that are not representative for the condition of interest are easily introduced during sample harvesting and work-up. In order to avoid these unwanted changes we have validated a -45 degrees C methanol-based quenching method for obtaining reliable and reproducible 'snapshot' samples of Lactobacillus plantarum cells for transcriptome analyses. Transcript profiles of cells harvested with the quenching method were compared with transcript profiles of cells that were harvested according to two different commonly applied protocols. Significant differences between the transcript profiles of cells harvested by the different methods from the same steady-state culture were observed. In total. 42 genes or operons were identified from which the transcript levels were altered when the cells were not immediately quenched upon harvesting. Among these, several have previously been associated with cold-shock response. Furthermore, the reproducibility of transcript profiles improved, as indicated by the fact that the variation in the data sets obtained from the quenched cells was smaller than in the data sets obtained from the cells that were harvested under non-quenched conditions. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:207 / 216
页数:10
相关论文
共 26 条
[1]   Global analysis of mRNA decay and abundance in Escherichia coli at single-gene resolution using two-color fluorescent DNA microarrays [J].
Bernstein, JA ;
Khodursky, AB ;
Lin, PH ;
Lin-Chao, S ;
Cohen, SN .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (15) :9697-9702
[2]   The genome-wide transcriptional responses of Saccharomyces cerevisiae grown on glucose in aerobic chemostat cultures limited for carbon, nitrogen, phosphorus, or sulfur [J].
Boer, VM ;
de Winde, JH ;
Pronk, JT ;
Piper, MDW .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (05) :3265-3274
[3]   A METHOD FOR THE DETERMINATION OF CHANGES OF GLYCOLYTIC METABOLITES IN YEAST ON A SUBSECOND TIME SCALE USING EXTRACTION AT NEUTRAL PH [J].
DEKONING, W ;
VANDAM, K .
ANALYTICAL BIOCHEMISTRY, 1992, 204 (01) :118-123
[4]   GROE MUTANTS OF ESCHERICHIA-COLI ARE DEFECTIVE IN UMUDC-DEPENDENT UV MUTAGENESIS [J].
DONNELLY, CE ;
WALKER, GC .
JOURNAL OF BACTERIOLOGY, 1989, 171 (11) :6117-6125
[5]   Cluster analysis and display of genome-wide expression patterns [J].
Eisen, MB ;
Spellman, PT ;
Brown, PO ;
Botstein, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (25) :14863-14868
[6]   Cold shock stress-induced proteins in Bacillus subtilis [J].
Graumann, P ;
Schroder, K ;
Schmid, R ;
Marahiel, MA .
JOURNAL OF BACTERIOLOGY, 1996, 178 (15) :4611-4619
[7]   Transcriptional and post-transcriptional control of cold-shock genes [J].
Gualerzi, CO ;
Giuliodori, AM ;
Pon, CL .
JOURNAL OF MOLECULAR BIOLOGY, 2003, 331 (03) :527-539
[8]   Benefits and pitfalls of using microarrays to monitor bacterial gene expression during infection [J].
Hinton, JCD ;
Hautefort, I ;
Eriksson, S ;
Thompson, A ;
Rhen, M .
CURRENT OPINION IN MICROBIOLOGY, 2004, 7 (03) :277-282
[9]   Genome-wide transcriptional profiling of the Bacillus subtilis cold-shock response [J].
Kaan, T ;
Homuth, G ;
Mäder, U ;
Bandow, J ;
Schweder, T .
MICROBIOLOGY-SGM, 2002, 148 :3441-3455
[10]   Trigger factor is induced upon cold shock and enhances viability of Escherichia coli at low temperatures [J].
Kandror, O ;
Goldberg, AL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (10) :4978-4981