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Status |
Public on Dec 01, 2012 |
Title |
13813_1 |
Sample type |
RNA |
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|
Source name |
mutant infected root
|
Organism |
Medicago truncatula |
Characteristics |
line: a17 age: 3 day bacterial strain: GRS138 bacterial genotype: GALA7 mutant
|
Treatment protocol |
Name:GRS138 - nothing - pathogen infection,ralstonia solanacearum strain grs138:time 13hour . - 3 plates of 12 roots/plate were inoculated with 300ul inoculum/root. - Inoculum 10^7cfu/ml
|
Growth protocol |
roots - - germination on water agar (4 days 4°C; 1 day 14°C) - root growth on Fahraeus medium with N-source; 3 days pre-culture in vitro before inoculation in vitro - 25°C; 75% RH;
|
Extracted molecule |
total RNA |
Extraction protocol |
13813_1:31ug. Standard Affymetrix Protocol
|
Label |
Biotin
|
Label protocol |
labelling Biotin direct, amplification=yes, cRNA 20 ug.
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|
|
Hybridization protocol |
labelled extract quantity: 15ug. Standard Affymetrix Protocol
|
Scan protocol |
GCOS, Biotin:pmt voltage 570nm,650V,laser power 1
|
Description |
We have identified two essential virulence determinants (GALA7, a type III secretion effector and HpaP, a chaperone-like protein) of Ralstonia solanacearum for the infection and colonisation of the host plant Medicago truncatula1,2. The scope of this project is to identify the GALA7 and HpaP-specific transcriptome alteration. For this purpose wild type and mutant infected root material (13h and 72h postinfection) will be analysed on M. truncatula affymetrix chips
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Data processing |
The data were normalized with the gcrma algorithm (Irizarry et al., 2003), available in the Bioconductor package (Gentleman and Carey, 2002).
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Submission date |
May 25, 2010 |
Last update date |
Dec 01, 2012 |
Contact name |
stephanie huguet |
E-mail(s) |
huguet@evry.inra.fr
|
Organization name |
inra
|
Street address |
2 rue gaston cremieux
|
City |
evry |
ZIP/Postal code |
91000 |
Country |
France |
|
|
Platform ID |
GPL4652 |
Series (1) |
GSE21985 |
Ralstonia solanacearum effector-specific effect on Medicago truncatula trancriptome |
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