NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM763612 Query DataSets for GSM763612
Status Public on Jun 23, 2014
Title S. cerevisiae Fermol cryophile replicate A, fermentation at 28C
Sample type RNA
 
Channel 1
Source name yeast cells from wine fermentation at 28C
Organism Saccharomyces cerevisiae
Characteristics strain: Fermol cryophile
growth phase: Beginning of stationary phase
Growth protocol Wine fermentations in Tempranillo must at 12C or 28C
Extracted molecule total RNA
Extraction protocol RNA extraction method was based on consecutive treatments with phenol-tris, phenol-chloroform (5:1) and chloroform-isoamyl alcohol (24:1) and a final precipitation with ethanol and sodium acetate (Garcia-Martinez et al., 2004).
Label Cy3
Label protocol 2-4 ug of total RNA was linearly amplified using the Low RNA Input Fluorescent Linear Amplification kit (Agilent Technologies™, Ca, USA). 2-3 ug of amplified cRNA was used as template for cDNA synthesis. cDNA was marked indirectly with “SuperScript™ Indirect cDNA Labeling System” (Invitrogen™, SanDiego, CA). The fluorophores used were Cy3 and Cy5 mono-reactiveDye (Amersham GE Healthcare™, Amersham UK) and dye incorporation was monitored by a Nanodrop spectrophotometer.
 
Channel 2
Source name yeast cells from wine fermentation at 28C
Organism Saccharomyces cerevisiae
Characteristics strain: Lalvin T73
growth phase: Beginning of stationary phase
Growth protocol Wine fermentations in Tempranillo must at 12C or 28C
Extracted molecule total RNA
Extraction protocol RNA extraction method was based on consecutive treatments with phenol-tris, phenol-chloroform (5:1) and chloroform-isoamyl alcohol (24:1) and a final precipitation with ethanol and sodium acetate (Garcia-Martinez et al., 2004).
Label Cy5
Label protocol 2-4 ug of total RNA was linearly amplified using the Low RNA Input Fluorescent Linear Amplification kit (Agilent Technologies™, Ca, USA). 2-3 ug of amplified cRNA was used as template for cDNA synthesis. cDNA was marked indirectly with “SuperScript™ Indirect cDNA Labeling System” (Invitrogen™, SanDiego, CA). The fluorophores used were Cy3 and Cy5 mono-reactiveDye (Amersham GE Healthcare™, Amersham UK) and dye incorporation was monitored by a Nanodrop spectrophotometer.
 
 
Hybridization protocol A mixture of 200 to 300 pmol of the two samples labelled was concentrated in a Concentrator Plus (Eppendorf™, Hamburg, Germany). Competitive hybridization was performed in hybridization chambers AHC (ArrayIt Corporation, CA, USA) at 42°C overnight. (Prehybridization solution contained 3X SSC, 0.1% SDS and 0.1 mg/ml BSA; hybridization solution contained 5X SSC, 0.1% SDS and 0.1 mg/ml of salmon DNA. Microarrays were washed manually with different solutions containing different SSC 20X and SDS 10% concentrations (Sol.1: 2X SSC-0.1% SDS; Sol.2: 0.1X SSC-0.1% SDS; Sol.3: 0.1 SSC; Sol4: 0.01X SSC).
Scan protocol Signal intensities of Cy3 and Cy5 were acquired with an Axon GenePix 4100A scanner (Molecular devices, CA, USA) using GenePix Pro v.6.1 software, at a resolution of 10 μm.
Description Gene expression of S. cerevisiae Fermol Cryophile with respect to the reference strain S. cerevisiae Lalvin T73. Samples from wine fermentation at 28C. Replicate A
Data processing Raw data with a global background subtraction were generated from GenePix pro 6.0. Analyses were done using Acuity 4.0 software (Molecular Devices, CA, USA).The individual data sets were normalized to a log2 ratio value of 1. After normalization, data were filtered to remove spots flagged as not found. Only spots with at least two replicates were considered. Finally, replicates were combined and their medians were calculated.
Genes with a two-fold log2 ratio values were considered to be significantly expressed.
 
Submission date Jul 19, 2011
Last update date Jun 24, 2014
Contact name Amparo Gamero
E-mail(s) amparo.gamerolluna@gmail.com
Organization name IATA-CSIC
Department Food Biotechnology
Street address Avda. Agustín Escardino 7
City Paterna
State/province Valencia
ZIP/Postal code 46980
Country Spain
 
Platform ID GPL13945
Series (1)
GSE30778 Molecular Analysis of the Genes Involved in Aroma Synthesis in the Species S. cerevisiae, S. kudriavzevii and S. bayanus var. uvarum in Winemaking

Data table header descriptions
ID_REF
VALUE normalized log2 ratio Cy3/Cy5

Data table
ID_REF VALUE
3XSSC 1.985
Arabidopsis 1.054
YAL001C -0.439
YAL002W 0.474
YAL003W -1.713
YAL004W 0.85
YAL005C -1.03
YAL007C -1.319
YAL008W -0.481
YAL009W -0.512
YAL010C -0.772
YAL011W -0.019
YAL012W -0.842
YAL013W -0.121
YAL014C 0.208
YAL015C -2.179
YAL016W -0.592
YAL017W 0.263
YAL018C
YAL019W -0.491

Total number of rows: 6191

Table truncated, full table size 86 Kbytes.




Supplementary file Size Download File type/resource
GSM763612.gpr.gz 1.1 Mb (ftp)(http) GPR
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap