|
| Status |
Public on Feb 24, 2019 |
| Title |
Parental strain, replicate1 |
| Sample type |
RNA |
| |
|
| Source name |
MDS42 strain
|
| Organism |
Escherichia coli |
| Characteristics |
genotype: control
|
| Treatment protocol |
Exponentially growing cultures (OD600 of ~1; mid-exponential growth phase) grown in the modified M9 medium were harvested for total RNA extraction.
|
| Growth protocol |
MDS42 and the ΔrecA mutant cells were inoculated from the frozen glycerol stock into 5 ml of modified M9 medium in test tubes and cultivated overnight at 34°C at 150 rpm. The overnight cultures were diluted to an OD600 of 0.1 into fresh modified M9 medium in test tubes and cultured.
|
| Extracted molecule |
total RNA |
| Extraction protocol |
Two volumes of RNA Protect bacterial reagent (Qiagen) were added directly to one volume of the exponentially growing cultures to stabilize cellular RNA. The cells were harvested by centrifugation at 5,000×g for 10 min at 25°C, and total cellular RNA was isolated using the RNeasy Mini Kit (Qiagen) according to the manufacturer’s instructions. Total RNA was treated with DNase I at room temperature for 15 min. The purified RNA samples were stores at – 80°C before microarray experiments. The quality of the purified RNA was evaluated using Agilent 2100 Bioanalyzer with an RNA 6000 Nano kit (Agilent Technologies). Only purified RNAs that had RIN (RNA integrity number) of 8.4 or more were utilized. The purified RNAs were stored at −80°C prior to transcriptome analysis.
|
| Label |
Cy3
|
| Label protocol |
100 ng of purified total RNA samples were labelled using the Low Input Quick Amp WT Labeling Kit (Agilent Technologies) with Cyanine3 (Cy3) according to the manufacturer’s instructions.
|
| |
|
| Hybridization protocol |
After confirmation of yields (> 825 ng) and specific activities (> 15 pmol/μg) of the Cy3-labbeled cRNAs using NanoDrop ND-2000, 600 ng of Cy3-labelled cRNA was fragmented at 60°C for 30 minutes in a reaction volume of 25 ul containing 1x Agilent fragmentation buffer and 2x Agilent blocking agent following the manufacturers instructions. On completion of the fragmentation reaction, 25 ul of 2x GE Hybridization Buffer HI-RPM was added to the fragmentation mixture and hybridized to custom designed the Agilent 8× 60K arrays for E. coli W3110, E.coli_K12_Expression_Ver.1, for 17 hours at 65°C in a rotating Agilent hybridization oven. After hybridization, microarrays were washed 1 minute at room temperature with GE Wash Buffer 1 (Agilent) and 1 minute with 37°C GE Wash buffer 2 (Agilent), then dried immediately.
|
| Scan protocol |
Slides were scanned immediately after washing on the Agilent SureScan Microarray Scanner (G4900DA) using one color scan setting for 8x60k array slides (AgilentG3_GX_1Color, Scan Area 61x21.6 mm, Scan resolution 5um, Dye channel is set to Green and Green PMT is set to 100%).
|
| Description |
Gene expression of E. coli cells at mid-exponential growth phase
|
| Data processing |
The scanned images were analyzed with Feature Extraction Software 10.7.3.1 (Agilent) using default parameters (protocol GE1_107_Sep09 and Grid: ExternalFullGEML_043017_D_F_20120907) to obtain background subtracted and spatially detrended Processed Signal intensities.
|
| |
|
| Submission date |
Oct 15, 2018 |
| Last update date |
Feb 24, 2019 |
| Contact name |
Chiara Furusawa |
| E-mail(s) |
[email protected]
|
| Phone |
+81-(0)6-6155-0456
|
| Organization name |
RIKEN Quantitative Biology Center
|
| Street address |
Furuedai
|
| City |
Suita |
| State/province |
Osaka |
| ZIP/Postal code |
565-0874 |
| Country |
Japan |
| |
|
| Platform ID |
GPL18948 |
| Series (1) |
| GSE121218 |
High-throughput identification of the impact of ΔrecA mutation on sensitivities to various chemical compounds in Escherichia coli |
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