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Sample GSM758874 Query DataSets for GSM758874
Status Public on Jul 13, 2011
Title sef1Δ mutant vs Wild type, in YEPD+BPS low iron medium, replicate 3
Sample type RNA
 
Channel 1
Source name Wild type grown in YEPD+BPS (low iron)
Organism Candida albicans
Characteristics strain: SN250
genotype/variation: wild type
Growth protocol Saturated overnight cultures of sef1Δ (SN330), hap43Δ (SN694), sfu1Δ (SN515), and isogenic wild type C. albicans (SN250) were inoculated into YPD to OD600=10-4 and incubated with shaking at 30ºC. The next morning, logarithmically growing cells were diluted to OD600 0.01 in iron-replete (wild type and sfu1Δ) or low iron (wild type, sef1Δ, and hap43Δ) medium and incubated at 30°C for 5-6 hours before harvesting at OD600=0.5-0.6. 5-6 biological replicates were performed per strain per condition.
Extracted molecule total RNA
Extraction protocol Total RNA was prepared using a hot phenol method (Miller and Johnson, 2002).
Label Cy3
Label protocol 10 μg of each RNA was treated with DNase I (Turbo DNA-free kit, Ambion) and reverse transcribed using aminoallyl-dUTP and Superscript II (Invitrogen) according to manufacturers’ instructions. cDNA was labeled with Cy3 and Cy5 (Amersham)
 
Channel 2
Source name sef1Δ grown in YEPD+BPS (low iron)
Organism Candida albicans
Characteristics strain: SN330
genotype/variation: sef1Δ
Growth protocol Saturated overnight cultures of sef1Δ (SN330), hap43Δ (SN694), sfu1Δ (SN515), and isogenic wild type C. albicans (SN250) were inoculated into YPD to OD600=10-4 and incubated with shaking at 30ºC. The next morning, logarithmically growing cells were diluted to OD600 0.01 in iron-replete (wild type and sfu1Δ) or low iron (wild type, sef1Δ, and hap43Δ) medium and incubated at 30°C for 5-6 hours before harvesting at OD600=0.5-0.6. 5-6 biological replicates were performed per strain per condition.
Extracted molecule total RNA
Extraction protocol Total RNA was prepared using a hot phenol method (Miller and Johnson, 2002).
Label Cy5
Label protocol 10 μg of each RNA was treated with DNase I (Turbo DNA-free kit, Ambion) and reverse transcribed using aminoallyl-dUTP and Superscript II (Invitrogen) according to manufacturers’ instructions. cDNA was labeled with Cy3 and Cy5 (Amersham)
 
 
Hybridization protocol Fluorescently labeled cDNAs from mutants were directly hybridized against those from wild type grown under the same conditions; dye flip controls were included. 6 additional arrays were performed using wild type grown under iron-replete vs. iron-limiting conditions. cDNA was labeled with Cy3 and Cy5 (Amersham), and 0.5 μg of each channel was hybridized to custom Agilent C. albicans ORF arrays (15,000 spots/array, 70-mer probes) following a protocol described by Hernday et al. (Methods Enzymol. 2010;470:737-58)
Scan protocol Arrays were scanned using a Genepix 4000A Axon scanner, and spots were filtered using GenePix Pro software.
Description Biological replicate 3 of 6. Low iron, Wt vs sef1DD
Data processing Data were normalized using Goulphar (LOWESS normalization) and subjected to One-class Significance Analysis of Microarrays (SAM) analysis with a median false discovery rate of 0.1%. Candidates meeting SAM criteria were also required to exhibit median 2-fold changes among 5-6 experiments.
 
Submission date Jul 12, 2011
Last update date Jul 13, 2011
Contact name Changbin Chen
E-mail(s) Changbin.Chen@ucsf.edu
Phone 4154768992
Fax 4154768201
Organization name University of California, San Francisco
Department Department of Microbiology & Immunology
Lab Dr. Suzanne Noble LAB
Street address HSE450, 513 Parnassus Avenue
City San Francisco
State/province California
ZIP/Postal code 94143
Country USA
 
Platform ID GPL13813
Series (2)
GSE30590 A unique iron homeostasis regulatory circuit with reciprocal roles in Candida albicans commensalism and pathogenesis [Expression Array]
GSE30593 A unique iron homeostasis regulatory circuit with reciprocal roles in Candida albicans commensalism and pathogenesis

Data table header descriptions
ID_REF
VALUE normalized log10 ratio representing test/reference

Data table
ID_REF VALUE
740 0.1285
3657 0.039
11229 -0.06
9819 0.2845
5038 -0.2395
7237 -0.3885
7535 -0.2725
14182 -0.274
14862 -0.136
487 0.325
2154 -0.191
4213 0.2345
2398 -0.2485
1723 -1.516
14056 -0.6455
5055 -0.132
7171 0.1095
9489 0.0595
10574 -0.0405
11113 -0.2815

Total number of rows: 6099

Table truncated, full table size 73 Kbytes.




Supplementary file Size Download File type/resource
GSM758874_sef1KO-L_rep3.gpr.gz 1.5 Mb (ftp)(http) GPR
Processed data included within Sample table

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