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Sample GSM1816208 Query DataSets for GSM1816208
Status Public on Sep 30, 2016
Title 10_Leaves_Montepulciano_Stress 1_Sampling1
Sample type RNA
 
Source name Montepulciano leaves collected two days after water deprivation, replicate 1
Organism Vitis vinifera
Characteristics cultivar: Montepulciano
tissue: Leaves
treatment: Water stress
sampling: Sampling 1, Two 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) marianna.fasoli@univr.it
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 245.5093
CHR10_GSVIVT00007268001_T01 478.8424
CHR10_GSVIVT00021093001_T01 168.2755
CHR10_GSVIVT00021115001_T01 62.3064
CHR10_GSVIVT00021131001_T01 1168.3412
CHR10_GSVIVT00021157001_T01 393.8718
CHR10_GSVIVT00021158001_T01 410.2985
CHR10_GSVIVT00021206001_T01 104.0781
CHR10_GSVIVT00021217001_T01 945.818
CHR10_GSVIVT00021273001_T01 112.5473
CHR10_GSVIVT00021290001_T01 92.3438
CHR10_GSVIVT00021333001_T01 57.5476
CHR10_GSVIVT00021341001_T01 145.226
CHR10_GSVIVT00021361001_T01 41.2603
CHR10_GSVIVT00021408001_T01 271.7596
CHR10_GSVIVT00021438001_T01 9105.9002
CHR10_GSVIVT00021476001_T01 4260.1286
CHR10_GSVIVT00021483001_T01 7940.0672
CHR10_GSVIVT00021487001_T01 12182.4156
CHR10_GSVIVT00021498001_T01 50.8259

Total number of rows: 29971

Table truncated, full table size 874 Kbytes.




Supplementary file Size Download File type/resource
GSM1816208_010_A10_531360_532.pair.gz 2.1 Mb (ftp)(http) PAIR
Processed data included within Sample table

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