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Sample GSM1318614 Query DataSets for GSM1318614
Status Public on May 19, 2015
Title Control HeLa Cells-non-polysomal-REP1
Sample type RNA
Source name Control HeLa Cells-non-polysomal
Organism Homo sapiens
Characteristics cell line: Adherent HeLa cells
genotype: Normal
rna fraction: Non-polysomal
Growth protocol Adherent HeLa cells were cultured under standard conditions. The TIA1 and TIAR shRNA-pSUPER constructs were generated with the pSUPER RNA interference (RNAi) System (OligoEngine, USA). Briefly, to knock-down TIA1 and TIAR, we have followed previously described methods (OligoEngine, USA) to generate TIA1 and TIAR short hairpin RNA (shRNA) pSUPER or empty pSUPER constructs from pSUPER.retro vectors. Sequences coding for short hairpin RNAs were inserted as double-stranded oligos followed by a short spacer, the reverse complement of the sense strand and five thymidines as an RNA polymerase III transcriptional stop signal into pSUPER vectors using the BglII and XhoI sites. The target sequences for the TIA1 and TIAR genes were 5'-AAGCTCTAATTCTGCAACTCT-3' and 5'-AACCATGGAATC AACAAGGAT-3', respectively. The configuration of the constructs was verified by DNA sequencing. The TIA1 and TIAR shRNA pSUPER constructs and the empty pSUPER vector as control were transfected into the cell line HeLa (1 μg of DNA/1×106 cells). Stable cell lines expressing empty or TIA1 and/or TIAR shRNA-pSUPER constructs were selected by plating for 3 weeks according to the manufacturer’s instructions (OligoEngine, USA). Clonal lines were isolated with cloning cylinders and verified by Western blotting.
Extracted molecule total RNA
Extraction protocol RNA from above HeLa cell lines was isolated and purified by using RNeasy kit (Qiagen). The quality of the RNAs was tested using the Agilent 2100 Bioanalyzer RNA Nano Chip
Label Cy3
Label protocol Total RNA (200 ng) was amplified using One Color Low Input Quick Amp Labeling Kit (Agilent Technologies) and purified with RNeasy Mini Kit (Qiagen). Preparation of probes and hybridization was performed as described One-Color Microarray Based Gene Expression Analysis Manual Ver. 6.5, Agilent Technologies.
Hybridization protocol The samples were placed on ice and quickly loaded onto arrays, hybridized at 65ºC for 17 hours in a Hybridization oven rotator and then washed in GE wash buffer 1 at room temperature (1 minute) and in GE Wash Buffer 2 at 37ºC (1 minute).
Scan protocol Images were captured with an Agilent Microarray Scanner and spots quantified using Feature Extraction Software (Agilent Technologies).
Description Control HeLa Cells-non-polysomal-REP1
Data processing Raw intensities were background-corrected by normexp method with an offset of 50. Background-corrected signals were log2 transformed and normalized by quantile adjustment as described in limma package of bioconductor.
Submission date Jan 30, 2014
Last update date May 21, 2015
Contact name Juan Carlos Oliveros
Organization name CNB, CSIC
Street address Darwin 3
City Cantoblanco
State/province Madrid
ZIP/Postal code 28049
Country Spain
Platform ID GPL13607
Series (1)
GSE54540 TIA proteins drives global and specific translational repression of genes linked to the cell-cycle progression and DNA replication/repair

Data table header descriptions
VALUE Normalized log2signals

Data table
1 13.35
2 5.9
3 5.98
4 7.73
5 7.99
6 6.53
7 12.12
8 9.07
9 6.26
10 5.96
11 6.13
12 8.25
13 8.36
14 7.61
15 11.88
16 5.94
17 6.55
18 6.06
19 6.11
20 7.39

Total number of rows: 62976

Table truncated, full table size 661 Kbytes.

Supplementary file Size Download File type/resource
GSM1318614_np_phi_I_1_252800416098_S01_GE1_107_Sep09_1_1.txt.gz 12.4 Mb (ftp)(http) TXT
Processed data included within Sample table

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