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Series GSE36558 Query DataSets for GSE36558
Status Public on Jun 01, 2012
Title affy_med_2011_06-Analysis of the Medicago noot mutant
Platform organisms Sinorhizobium meliloti; Medicago sativa; Medicago truncatula
Sample organism Medicago truncatula
Experiment type Expression profiling by array
Summary affy_med_2011_06 - affy_med_2011_06 - Legume plants establish a symbiotic interaction with soil bacteria called rhizobia. A complex molecular dialogue between the two partners is necessary for the successful infection and organogenesis processes that will ultimately result in the formation of a nitrogen fixing nodule. During a M. truncatula Tnt1 mutant screen, a new class of symbiotic mutant called noot (nodule root) was identified. This original single recessive mutant develops a root in apical position of nodules that are colonized by bacteria and functional for nitrogen fixation. This conversion suggests that the legume nodule morphogenetic pathway may be derived from a root program. We cloned the NOOT gene and showed that it corresponds to Pisum sativum COCH (Ferguson and Reid, 2005, Plant Cell Physiol 46, 1583-1589). The goal of this project is to compare the transcriptomes from wild type nodules and roots to the noot nodule one. This will allow us to unravel the similarity and differences between the wild type and mutant nodule transcriptomes but also to know which developmental pathway is under the control of the NOOT gene. --Seeds of the WT and noot mutant lines (two mutant alleles: Tnk507 and NF2717) were surface sterilized and placed at 4°C for three days on a minimal BNM medium square plate (12cm X 12cm). Seeds were germinated at room temperature and 10 seeds were placed in a row on nitrogen poor (BNM) plate. Seedlings were inoculated using Sinorhizobium meliloti Rm41 for nodule production. Some WT plants were not infected by the bacteria in order to collect roots. Nodules and roots were harvested 18 to 21 days post inoculation. Each experimental repetition (3 WT nodules, 3 WT roots and 2 mutant nodules of each allele) was harvested at a separated day. RNA preparations were done using a Quiagen Kit.
 
Overall design 10 arrays - Medicago; gene knock out,organ comparison
Web link http://urgv.evry.inra.fr/CATdb
 
Contributor(s) Ratet P, Mondy S, Huguet S, Balzergue S, Martin-Magniette M
Citation missing Has this study been published? Please login to update or notify GEO.
Submission date Mar 16, 2012
Last update date Jun 02, 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
 
Platforms (1)
GPL4652 [Medicago] Affymetrix Medicago Genome Array
Samples (10)
GSM896883 R108N_2 with array type Medicago from Affymetrix
GSM896884 R108R_1 with array type Medicago from Affymetrix
GSM896885 R108N_3 with array type Medicago from Affymetrix
Relations
BioProject PRJNA153435

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE36558_RAW.tar 39.2 Mb (http)(custom) TAR (of CEL)
Processed data included within Sample table

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