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Series GSE6552 Query DataSets for GSE6552
Status Public on Dec 25, 2006
Title Transcriptome associates with rice organogenesis
Organism Oryza sativa
Experiment type Expression profiling by array
Summary Most plant cells retain the capacity to differentiate into all the other cell and organ types that constitute a plant. However, genome-wide transcriptional activities underlying the process of cell differentiation are poorly understood, especially in monocot plants. Here we used a rice (Oryza sativa) cell culture system to generate somatic embryos, which were further induced into shoots and roots. The global transcriptional reorganization during the development of somatic embryos, shoots, and roots from cultured cells was studied using a rice whole genome microarray and verified by RNA blotting analysis of representative genes. Overall, only 1-3% of expressed genes were differentially regulated during each organogenesis process at the examined time point. Also metabolic pathways were minimally regulated. Thus the genes that dictating organ formation should be relatively small in number. Comparison of these three transcriptomes revealed little overlap during these three organogenesis processes. These results indicate that each organogenesis involves specific reorganization of genome expression.
Keywords: transcriptome
 
Overall design Oryza sativa Genome Oligo Set Version 1.0 was designed by Beijing Genomics Institute (BGI) and contain 60,727 70mer oligos representing both indica and japonica genomes. All oligos were designed from cDNAs, expreseed sequence tag (EST) sequences, predicted genes of BGI rice genome build and other public resources. Mapping to TIGR rice genome pseudommolecues release 2 is based on the BLAST results, if a oligo has greater than 97% identity to a gene sequence from TIGR pseudomolecules, the oligo represents that gene. Rice 30K Operon Version 1.0 -70 mer oligos. The array is in 48 pin conformation. It has 25 columns and 25 rows in each of 4 x 12 subarrays.
 
Contributor(s) Su N, He K, Jiao Y, Deng X
Citation(s) 17072560
Submission date Dec 17, 2006
Last update date Sep 17, 2012
Contact name Kun He
E-mail(s) hek@mail.cbi.pku.edu.cn
Phone 203-432-8909
Organization name Yale University
Department Molecular, Cellular & Developmental Biology
Lab Denglab
Street address 165 Prospect
City New Haven
State/province CT
ZIP/Postal code 06520
Country USA
 
Platforms (2)
GPL1773 LIMA_SlideA
GPL1774 LIMA_SlideB
Samples (16)
GSM151641 Embryo vs. Callus AP1
GSM151642 Embryo vs. Callus AP2
GSM151643 Embryo vs. Callus AP3
Relations
BioProject PRJNA98785

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Supplementary file Size Download File type/resource
GSE6552_RAW.tar 31.7 Mb (http)(custom) TAR (of GPR)

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