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Sample GSM1816263 Query DataSets for GSM1816263
Status Public on Sep 30, 2016
Title 65_Berries_Sangiovese_Stress 1_Sampling3
Sample type RNA
 
Source name Sangiovese berries collected 27 days after water deprivation, replicate 2
Organism Vitis vinifera
Characteristics cultivar: Sangiovese
tissue: Berries
treatment: Water stress
sampling: Sampling 3, 27 days after water deprivation
Treatment protocol Ten vines per cultivar were used and maintained at about 90% of maximum water availability (WW, well watered vines) and 10 vines received, from fruit-set to veraison, 40% of maximum water availability (WS, water stressed vines) (Figure 1). During water limitation, all stressed vines were covered with a plastic film to avoid interference due to rainfall and soil water evaporation. Re-watering was performed 46 days after stress imposition and the post-recovery plant material (ex-WS) was collected after 24 days (i.e. 70 days after the onset of water stress).
Growth protocol This study was conducted in 2011 on eight-year-old potted (60 L) vines of cv. Sangiovese (clone VCR30) and cv. Montepulciano (clone R7) grafted onto 1103 Paulsen rootstock and grown in an outdoor area close to the Faculty of Agriculture of the University of Perugia (Region of Umbria, central Italy, 42°58’ N, 12°24’ E, altitude 405 m a.s.l.).
Extracted molecule total RNA
Extraction protocol Total RNA was extracted from ~50 mg of frozen leaves and ~200 mg of berry (pericarp plus seeds) using the Spectrum™ Plant Total RNA kit (Sigma-Aldrich, St. Louis, MO) with some modifications as reported in Fasoli, et al. (2012). RNA quality and quantity were assessed using a Nanodrop 2000 spectrophotometer (Thermo Scientific, Wilmington, DE) and a Bioanalyzer Chip RNA 7500 series II (Agilent, Santa Clara, CA).
Label Cy3
Label protocol cDNA synthesis and labeling reactions were performed according to the NimbleGen Arrays User’s Guide (V 3.2).
 
Hybridization protocol Hybridization and washing procedures were performed according to the NimbleGen Arrays User’s Guide (V 3.2).
Scan protocol Each microarray was scanned using a Axon GenePix 4400 A at 532 nm (Cy-3 absorption peak) and GenePix Pro7 software (Molecular Devices, Sunnyvale, CA, USA) according to the manufacturers' instructions.
Data processing Images were analyzed using NimbleScan v2.5 software (Roche), background correction and standard RMA normalization were selected.
 
Submission date Jul 09, 2015
Last update date Sep 30, 2016
Contact name Marianna Fasoli
E-mail(s) [email protected]
Phone +39 045 842 5625
Organization name University of Verona
Department Biotechnology
Lab Molecular Viticulture
Street address Via della Pieve 70
City San Pietro in Cariano
State/province Verona
ZIP/Postal code 37029
Country Italy
 
Platform ID GPL17894
Series (1)
GSE70670 Distinct transcriptome responses to water limitation in isohydric and anisohydric grapevine cultivars

Data table header descriptions
ID_REF
VALUE Nimblescan v2.5 software calculated RMA-normalized signal intensities.

Data table
ID_REF VALUE
CHR10_GSVIVT00006725001_T01 350.0701
CHR10_GSVIVT00007268001_T01 293.7016
CHR10_GSVIVT00021093001_T01 537.4091
CHR10_GSVIVT00021115001_T01 57.68
CHR10_GSVIVT00021131001_T01 807.5298
CHR10_GSVIVT00021157001_T01 488.0086
CHR10_GSVIVT00021158001_T01 843.2257
CHR10_GSVIVT00021206001_T01 236.7806
CHR10_GSVIVT00021217001_T01 395.1642
CHR10_GSVIVT00021273001_T01 373.5409
CHR10_GSVIVT00021290001_T01 38.5414
CHR10_GSVIVT00021333001_T01 48.5789
CHR10_GSVIVT00021341001_T01 424.8709
CHR10_GSVIVT00021361001_T01 195.7505
CHR10_GSVIVT00021408001_T01 64.0683
CHR10_GSVIVT00021438001_T01 19117.9694
CHR10_GSVIVT00021476001_T01 915.8494
CHR10_GSVIVT00021483001_T01 645.582
CHR10_GSVIVT00021487001_T01 2723.4538
CHR10_GSVIVT00021498001_T01 72.9025

Total number of rows: 29971

Table truncated, full table size 874 Kbytes.




Supplementary file Size Download File type/resource
GSM1816263_065_A05_531336bis_532.pair.gz 2.2 Mb (ftp)(http) PAIR
Processed data included within Sample table

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