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Sample GSM956463 Query DataSets for GSM956463
Status Public on Jan 01, 2013
Title 18°C/400 µatm pluteus stage replicate 1
Sample type RNA
 
Channel 1
Source name Approx. 8,000 pooled larvae from one 18°C/400 µatm culture replicate
Organism Strongylocentrotus purpuratus
Characteristics Stage: Pluteus
culture conditions: 18°C/400
Treatment protocol pCO2 within each culture was manipulated by bubbling CO2 gas into seawater as described in Fangue et al. (2010). Temperature was controlled by placing culture mesocosms in baths containing seawater at 13°C or 18°C.
Growth protocol Ferilized eggs were cultured under four different seawater pCO2 concentrations and temperatures: (i)13°C/400 µatm pCO2, (ii)13°C/1100 µatm pCO2, (iii)18°C/400 µatm pCO2 (iv)18°C/1100 µatm pCO2. Larval cultures were performed as described in Fangue et al. (2010). A laboratory-based, experimental system for the study of ocean acidification effects on marine invertebrate larvae. Limnology and Oceanography: Methods 8: 441–452.
Extracted molecule total RNA
Extraction protocol Total RNA extracted using Trizol following manufacturer's instructions.
Label Cy5
Label protocol 200 ng of clean, total RNA from either experimental or reference samples were amplified and labeled with Cy5 or Cy3 fluorescent dyes, respectively, using Agilent's Low-Input Quick Amp Two Color Labeling Kit (#5190-2306, Agilent Technologies Inc., Santa Clara, CA, USA).
 
Channel 2
Source name Total RNA pooled from aliquots of total RNA from all experimental samples and labeled with Cyanine-3 (green).
Organism Strongylocentrotus purpuratus
Characteristics sample type: Reference
Treatment protocol pCO2 within each culture was manipulated by bubbling CO2 gas into seawater as described in Fangue et al. (2010). Temperature was controlled by placing culture mesocosms in baths containing seawater at 13°C or 18°C.
Growth protocol Ferilized eggs were cultured under four different seawater pCO2 concentrations and temperatures: (i)13°C/400 µatm pCO2, (ii)13°C/1100 µatm pCO2, (iii)18°C/400 µatm pCO2 (iv)18°C/1100 µatm pCO2. Larval cultures were performed as described in Fangue et al. (2010). A laboratory-based, experimental system for the study of ocean acidification effects on marine invertebrate larvae. Limnology and Oceanography: Methods 8: 441–452.
Extracted molecule total RNA
Extraction protocol Total RNA extracted using Trizol following manufacturer's instructions.
Label Cy3
Label protocol 200 ng of clean, total RNA from either experimental or reference samples were amplified and labeled with Cy5 or Cy3 fluorescent dyes, respectively, using Agilent's Low-Input Quick Amp Two Color Labeling Kit (#5190-2306, Agilent Technologies Inc., Santa Clara, CA, USA).
 
 
Hybridization protocol Amplified and labled RNA whose yield and specific activity exceeded 1.875 µg and 6 pmol, repsectively, were hybridized to each array according to instructions for Agilent's Two-Color Microarray-Based Gene Expression Analysis (Low Input Quick Amp Labeling) Protocol.
Scan protocol Scanned using an Axon GenePix 4000B microarray scanner, adjusting the PMT gain for optimized visualization of each slide.
Description Biological replicate 1 of 3 from 18°C/400 µatm sampled at pluteus stage
Data processing Agilent Feature Extraction Software (v 9.5.3.1) was used for background subtraction and LOWESS normalization. Only genes 2.6 times above background, but not saturated in all samples were analyzed. Different probes targeting the same gene loci (e.g. SPU) were summarized by computing the geometric mean.
 
Submission date Jul 05, 2012
Last update date Jan 01, 2013
Contact name Tyler G Evans
E-mail(s) tyler.evans@lifesci.ucsb.edu, tylergevans@gmail.com
Phone 8058936176
Fax 8058938062
Organization name University of California Santa Barbara
Department Ecology, Evolution and Marine Biology
Lab Hofmann
Street address Marine Science Institute
City Santa Barbara
State/province California
ZIP/Postal code 93106-9620
Country USA
 
Platform ID GPL15767
Series (1)
GSE39125 Synergistic effects of temperature and pCO2 on growth, development and gene expression of Strongylocentrotus purpuratus larvae

Data table header descriptions
ID_REF
VALUE lowess normalized test/reference

Data table
ID_REF VALUE
SPU_000008 0.428056899
SPU_000015 -0.064906609
SPU_000071 0.292721813
SPU_000091 0.581492898
SPU_000105 0.451676279
SPU_000225 -0.062610154
SPU_000335 -0.211064119
SPU_000354 -0.33827666
SPU_000465 -0.033155234
SPU_000494 0.797927115
SPU_000495 0.613444777
SPU_000682 -0.480130583
SPU_000694 -0.23166841
SPU_000753 0.018147055
SPU_000822 0.27410161
SPU_000825 -0.047697291
SPU_000908 -0.482717893
SPU_001158 0.040461208
SPU_001245 -0.242022429
SPU_001474 0.132142538

Total number of rows: 3627

Table truncated, full table size 82 Kbytes.




Supplementary file Size Download File type/resource
GSM956463_18-L-1.txt.gz 28.1 Mb (ftp)(http) TXT
Processed data included within Sample table

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