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Series GSE111468 Query DataSets for GSE111468
Status Public on May 22, 2019
Title The MYB5-driven MBW complex recruits a WRKY factor to enhance the expression of targets involved in vacuolar hyper-acidification and trafficking in grapevine
Organism Vitis vinifera
Experiment type Expression profiling by array
Summary The accumulation of secondary metabolites and the regulation of tissue acidity contribute to important traits like color, astringency and acidity of grape berry which are essential to the value of the final product, the wine. Moreover, they influence the plant performance in response to the environment and to parasites and herbivores. In several plant species highly conserved WD-MYB-bHLH-WRKY (WMBW) transcriptional complexes determine color and acidity in epidermal cells. Here we investigated the function in grapevine (Vitis vinifera L.) of WMBW complexes involving two MYBs (VvMYB5a and VvMYB5b) and the WRKY-type transcription factor VvWRKY26. Using transgenic grapevine plants we show that these complexes affect different aspects of morphology, plant development, pH regulation, and pigment accumulation. Transcriptomic analysis identified a core set of putative target genes controlled by VvMYB5a, VvMYB5b and VvWRKY26 in different tissues. Our data indicate that VvWRKY26 enhances the expression of selected target genes induced by VvMYB5a/b. Among these target genes are enzymes of the biosynthesis of flavonoids, genes involved in cell-type identity and the P-type ATPases VvPH5 and VvPH1. In addition, VvWRKY26 is recruited specifically by VvMYB5a, reflecting the functional diversification of VvMYB5a and VvMYB5b. The expression of WBMW complexes in vegetative organs, such as leaves, indicates a possible function of vacuolar hyper-acidification in repulsion of parasites/herbivores and/or in developmental processes as shown by defects in transgenic grape plants where the WMBW complex is inactivated.
 
Overall design Transcriptomic changes caused by the alteration of VvMYB5a, VvMYB5b and VvWRKY26 expression, were inspected by a microarray analysis performed on leaf RNA of selected transgenic lines and wild type plants. Three biological replicates of fully expanded leaves were collected before the onset of the altered phenotype in order to avoid secondary transcriptional effects.
 
Contributor(s) Amato A, Cavallini E, Walker AR, Pezzotti M, Bliek M, Quattrocchio FM, Koes R, Ruperti B, Bertini E, Zenoni S, Tornielli GB
Citation(s) 31125454
Submission date Mar 06, 2018
Last update date Aug 26, 2019
Contact name Alessandra Amato
E-mail(s) alessandra.amato@univr.it
Organization name University of Verona
Street address strada le grazie 15
City VR
ZIP/Postal code 37134
Country Italy
 
Platforms (1)
GPL17894 NimbleGen 090918 Vitus vinifera exp HX12 [090918_Vitus_exp; GENE_CALL_ID version]
Samples (21)
GSM3031723 WT_MYB5aOE_replicate 1
GSM3031724 WT_MYB5aOE_replicate 2
GSM3031725 WT_MYB5aOE_replicate 3
Relations
BioProject PRJNA437126

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
GSE111468_RAW.tar 53.2 Mb (http)(custom) TAR (of PAIR)
Processed data included within Sample table

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