NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM763609 Query DataSets for GSM763609
Status Public on Jun 23, 2014
Title S. uvarum CECT 12600 replicate A, fermentation at 12C
Sample type RNA
 
Channel 1
Source name yeast cells from wine fermentation at 12C
Organism Saccharomyces uvarum
Characteristics strain: CECT 12600
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 12C
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. uvarum CECT12600 with respect to the reference strain S. cerevisiae Lalvin T73. Samples from wine fermentation at 12C. 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 -1.24
Arabidopsis -1.606
YAL001C -2.832
YAL002W -2.573
YAL003W -0.889
YAL004W -1.439
YAL005C -0.121
YAL007C 0.289
YAL008W 0.07
YAL009W -1.035
YAL010C -0.69
YAL011W -2.73
YAL012W -1.258
YAL013W -2.593
YAL014C -2.203
YAL015C -0.478
YAL016W 0.168
YAL017W 0.067
YAL018C -2.409
YAL019W -1.667

Total number of rows: 6191

Table truncated, full table size 86 Kbytes.




Supplementary file Size Download File type/resource
GSM763609.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