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Sample GSM140626 Query DataSets for GSM140626
Status Public on Oct 19, 2006
Title Transcriptional profile of Candida glabrata ingested by macrophage cells for 2 hours (Experiment 3-2)
Sample type RNA
 
Channel 1
Source name C. glabrata medium control
Organism Nakaseomyces glabratus
Characteristics A wild type strain of C. glabrata, Cg462 was used in this experiment and it is routinely cultured in YPD medium at 30 C.
Treatment protocol C. glarata cells cultured in DMEM supplemented with 10 % FBS for 2 hrs.
Extracted molecule total RNA
Extraction protocol C. glabrata cells were disrupted with 0.5-mm glass beads (Fisher Scientific) in the presence of guanidium-isothiocyanate (GITC), and the total RNA was isolated by acid phenol extraction. The RNA was further purified by RNeasy Mini kit (Qiagen).
Label Cy5-cDNA
Label protocol 20 ug of total RNA was used to synthesize Cy5-cDNA probes with an anchor primer [(dT)18(dA/dG/dC)] in the presence of Cy5-dCTP (PerkinElmer) using SuperscriptTM III reverse transcriptase (Invitrogen). The probe was purified using MinElute TM reaction Cleanup kit (Qiagen) and vaccum dried.
 
Channel 2
Source name C. glabrata ingested by murine macrophage-like cells J774A.1 for 2 hours
Organism Nakaseomyces glabratus
Characteristics Murine macrophage-like cell line J774A.1 was purchased from ATCC and it is routinely cultured at 37 C in humidified 5 % CO2 atmosphere in Dulbecco's modified Eagle medium (DMEM) supplemented with 10% fetal bovine serum (FBS).
A wild type strain of C. glabrata, Cg462 was used in this experiment and it is routinely cultured in YPD medium at 30 C.
Treatment protocol J774A.1 macrophage-like cells were seeded in a 175 cm2 tissue culture flasks and cultured for 16-18 hrs till confluency. Log phase C. glabrata cells (about 2*107 cells/flask) were added onto the macrophage cells to a MOI of 1:1. The flask was spun down for 1 min at 1,000 rpm to bring the yeast cells down. The flask was incubated at 37 C. After 1 hr, the yeast cells that remained outside of macrophages were washed off with warm PBS, and fresh medium was added. At hour 2, the macrophages were lysed in ice-cold water containing RNase cocktail (Ambion Biotech)(to degrade the released macrophage RNA) for 5 min. The lysate was quickly spun down, washed twice with RNase-free water containing protectRNA TM RNase inhibitor (Sigma). Finally the yeast cell pellets from 6 flasks (1*108 cells total) was quickly frozen in liquid nitrogen for RNA prep.
Extracted molecule total RNA
Extraction protocol see in channel 1
Label Cy3-cDNA
Label protocol see in channel 1
 
 
Hybridization protocol Both Cy5- and Cy3- cDNA probes were resuspened into hybridization buffer (35% formamide, 5*SSC, 0.1%SDS, 0.1 mg/ml denatured salmon sperm DNA) and combined to a total volume of 40 ul. The probe mix was denatured at 100 C for 10 s and quickly cooled on ice, then it was added on a microarray slides. The slides was covered with a cover glass and incubated in a chamber (Corning) at 42 C for 16-18 hrs. The washing protocol follows the manual for UltraGAPS coated slides (Corning).
Scan protocol Hybridized slides was scaned by Axon 4000B microarray scanner with 100% power and PMT ranging 600-800. Data were acquired by Axon GenePix 5.0 software.
Description This is experiment 2 of a dye-swap experiment. Experiment 1 is deposited in GSM140625.
Data processing The median signal intensity captured from Cy5-channel (F635) and from Cy3-channel (F532) was used to calculate the C. glabrata gene expression ratio (Macrophage ingested/medium control
 
Submission date Oct 17, 2006
Last update date Oct 18, 2006
Contact name Brendan Cormack
E-mail(s) bcormack@jhmi.edu
Phone 410-955-3651
Organization name Johns Hopkins Univ. School of Medicine
Department Molecular Biology & Genetics
Street address Hunterian Building 617, 725 N. Wolfe St.
City Baltimore
State/province MD
ZIP/Postal code 21205
Country USA
 
Platform ID GPL3922
Series (1)
GSE6058 Transcriptional profile of Candida glabrata ingested by murine macrophage-like cells (J774A.1) for 2 and 6 hours

Data table header descriptions
ID_REF
VALUE Log2[Ratio of Medians(635/532)]
F635 Median The median of signal intensity from Cy5 channel
F532 Median The median of signal intensity from Cy3 channel
Ratio of Medians (635/532) Ratio of signal intensity (Cy5/Cy3)
Flags Quality information about each hybridized spot depending on the value of the flag. Unflagged spot is of good quality and has value 0. Spots with value -50 are of very low intensity which we discard for further analysis. Spots with value -75 corresponds to empty spots on the array.

Data table
ID_REF VALUE F635 Median F532 Median Ratio of Medians (635/532) Flags
1 -0.303 210 259 0.811 0
2 -0.469 185 256 0.723 0
3 -0.566 183 271 0.675 0
4 -0.802 148 258 0.574 0
5 -0.657 149 235 0.634 0
6 -0.883 148 273 0.542 0
7 -0.772 140 239 0.586 0
8 -0.943 129 248 0.520 0
9 -0.550 155 227 0.683 0
10 -0.316 180 224 0.804 0
11 -1.191 74 169 0.438 -50
12 -1.017 82 166 0.494 -50
13 0.420 546 408 1.338 0
14 0.512 455 319 1.426 0
15 0.523 434 302 1.437 0
16 0.466 384 278 1.381 0
17 0.726 463 280 1.654 0
18 0.752 453 269 1.684 0
19 -0.978 98 193 0.508 -50
20 -1.089 86 183 0.470 -50

Total number of rows: 13056

Table truncated, full table size 356 Kbytes.




Supplementary file Size Download File type/resource
GSM140626.gpr.gz 1.1 Mb (ftp)(http) GPR

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