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E-GEOD-16448 GSE16448 transcription profiling by array Crassostrea gigas

microarray_summer_mortality_insitu_oyster

Submitted June 4, 2009 ·Released Aug. 15, 2009 ·Updated May 1, 2014
16
Samples
8
Assays
1
Array Platforms
1
References
Description

Summer mortality of the Pacific oyster Crassostrea gigas is the result of a complex interaction between oysters, their environment and pathogens. Heredity appears to be a major factor determining the sensitivity of oysters to summer mortality, allowing resistant (R) and susceptible (S) lines to be produced. We conducted genome-wide expression profiling of R and S gonads during the 3-month period preceding a summer mortality event using a 9K cDNA microarray that we designed. This transcriptional analysis provides new indications to define markers for Quantitative Trait Loci searches and functional studies, and evaluates the potential role of each gene in the resistance to summer mortality For microarray analysis, R and S oysters were sampled four times (dates 1 to 4: May 9, May 25, June 6, and June 20, respectively). On each date, 3 replicates of 8 oysters were sampled from each line (R and S) and the gonads prepared for total RNA extraction. Furthermore, the entire tissues of 10 wild oysters were collected, pooled and homogenized to constitute a single total RNA sample for use as a reference in all slide hybridizations and RT-PCR analysis. For microarray hybridizations, 5µg of total RNA were directly labeled by reverse transcription and then purified using the Direct ShipShot Labeling kit (Promega). This reaction was performed for each of the 24 gonad samples, with Cy5 (red) incorporation. The reference sample was Cy3-labeled (green) in 24 separate tubes following the same protocol. The 24 Cy3-labeled cDNAs were next pooled, and then divided once more into 24 samples to obtain a homogeneous reference. Equimolar amounts of cDNA samples and cDNA reference labeled with Cy5 and Cy3, respectively, were SpeedVac evaporated and mixed into a single pool with the hybridization buffer (ChipHyb™ hybridization buffer, Ventana Discovery, Tucson, AZ, USA). They were then co-hybridized on the same microarray slide, in a Ventana hybridization station (Ventana Discovery, Tucson, AZ, USA). The data submitted here correspond to the mean of the three replicates for each line and each date, representing 8 samples : gonad_resistant_date1 gonad_sensitive_date1 gonad_resistant_date2 gonad_sensitive_date2 gonad_resistant_date3 gonad_sensitive_date3 gonad_resistant_date4 gonad_sensitive_date4

Array Platforms
A-GEOD-8639
MPI oyster gigas 9K v1.0(8 items)
Sample Attributes
BioSourceProvider
Laboratoire de Physiologie des Invertebres IFREMER Brest
field
Brest, France, in situ rearing (South Britanny, France)
gender
males and females
line
no selection (wild oysters), resistant, sensitive
Organism
Crassostrea gigas
sample
pool of 10 oysters, pool of 8 gonad oysters
sampling
1 month before the mortality peak, 1 week before the mortality peak, 10 days before the mortality peak, 2 weeks before the mortality peak, 3 weeks before the mortality peak, the 10th May 2007
tissue
all tissues (whole oyster), gonad
Experiment Info
Accession
E-GEOD-16448
GEO ID
GSE16448
Type
transcription profiling by array
Organism
Crassostrea gigas
Submitted
June 4, 2009
Released
Aug. 15, 2009
Updated
May 1, 2014
Submitter
Charlotte Corporeau、 Jeanne Moal、 Alain Hénaut、 Pascal Favrel、 David Mazurais、 JeanYves Daniel、 Arnaud Huvet、 Elodie Fleury、 Arnaud Huvet、 Pierre Boudry、 Viviane Boulo
Analysis Services
Analysis Services

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