GEO Accession viewer

NCBI > GEO > Accession Display

Not logged in | Login

GEO help: Mouse over screen elements for information.

Sample GSM5150566

Query DataSets for GSM5150566

Status

Public on Mar 23, 2021

Title

COLO205_selumetinib_CCNB1_+ve_1

Sample type

SRA

Source name

COLO205

Organism

Homo sapiens

Characteristics

cell type: colorectal cancer cell line
growth media: RPMI-1640 + 1uM selumetinib (24 hours)
cell line: COLO205
fixed/unfixed: Glyoxal fixed, stained for CCNB1 and sorted

Extracted molecule

polyA RNA

Extraction protocol

Cell pellets were lysed in 1 mL TRI reagent (Sigma, T9424) and mixed until a homogeneous lysate was obtained. For phase separation, 0.2 mL chloroform was added, mixed thoroughly and allowed to stand for 10 minutes prior to centrifugation at 12,000 × g for 15 min at 4 °C. The upper aqueous phase containing RNA was transferred to a fresh tube, and 0.5 mL 2-propanol per mL original lysate was then added, samples mixed and allowed to stand for 10 minutes. Samples were centrifuged (12,000 × g for 10 min at 4 °C), and RNA pellets washed with 1 mL 75% (v/v) ethanol (7,500 × g for 5 min at 4 °C). Pellets were air-dried for 5-10 minutes and resuspended in RNase-free water.
RNA prepared from flow sorted cells was quality controlled on a Bioanalyzer 2100 (Agilent) using RNA Pico 6000 chips (Agilent 5067-1513). mRNA-seq libraries were prepared using the NEBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB E7760S) with the NEBNext Poly(A) mRNA Magnetic Isolation Module (NEB E7490S), following the protocol provided by the manufacturer with the exception that two successive 0.9x AMPure purifications were performed on the final amplified libraries. All libraries were amplified using 12-14 PCR cycles. Library quality was assessed on a Bioanalyzer 2100 using High Sensitivity DNA chips (Agilent 5067-4626) and quantification performed with a KAPA Library Quantification Kit (Roche, KK4844). Libraries were sequenced by the Babraham Institute Next Generation Sequencing Facility on an Illumina HiSeq2500 in Rapid Run 50bp Single End mode.

Library strategy

RNA-Seq

Library source

transcriptomic

Library selection

cDNA

Instrument model

Illumina HiSeq 2500

Description

gene_expression_data_sorts.txt
Cells grown in monolayers were harvested by trypsinization, centrifuged (300 x g for 5 minutes) and washed once with PBS prior to lysis in TRI reagent. For glyoxal fixation and staining, cell pellets were resuspended in 100 µL glyoxal fixation solution (2.8 ml water, 0.79 ml 100% ethanol, 0.31 ml 40% glyoxal and 30 µl acetic acid, pH 4-5) supplemented with 1:25 RNasin Plus RNase inhibitor (Promega, N261B) and incubated for 15 minutes on ice. The cell suspension was diluted in 1 mL PBS supplemented with 1:100 RNasin Plus RNase inhibitor and centrifuged at 2000 x g for 3 minutes at 4°C; the supernatant was discarded. All further centrifugation steps were carried out at similar conditions. Cells were permeabilized by adding 100 µL ice-cold methanol (100%, v/v) with 1:25 RNasin Plus RNase inhibitor drop by drop while gently vortexing cells, and incubated on ice for 30 minutes. The cell suspension was then diluted in 1 mL 1% bovine serum albumin (BSA) (Sigma, A7906) in PBS and centrifuged. For EdU staining, cells were incubated in a modified click reaction cocktail (221.5 µL PBS, 2.5 µL CuSO4, 25 µL 1 M sodium ascorbate, 1.25 µL Alexa Fluor 488) Click-iT™ EdU Alexa Fluor™ 488 Flow cytometry kit (Thermo Fisher Scientific, C10420) and incubated for 30 minutes on ice in dark. Following incubation, cells were washed in 1% BSA in PBS and 1:25 RNasin Plus and incubated in 1 µg/mL DAPI in PBS. For CCNB1 labelling, cells were incubated in 100 uL primary antibody (in this case CST 12231S - 1:200) diluted in 1% BSA in PBS with 1:25 RNasin Plus RNase inhibitor for 1 hour on ice. Following incubation, cells were washed once in 1mL 1% BSA in PBS. Secondary antibody staining was carried out in 100 μL Alexa Fluor 488 donkey anti-rabbit antibody (ThermoFisher Scientific, A21206) diluted 1:1000 in 1% BSA in PBS with 1:25 RNasin Plus RNase inhibitor and incubated on ice for 30 minutes in dark. Cells were washed once in 1 mL 1% BSA in PBS and the cell pellet resuspended in 200 µL 1% BSA in PBS with 1:100 RNasin Plus RNase inhibitor. Cells were incubated in 1 µg/mL DAPI. For collection of glyoxal-fixed cells that were stained with EdU or CCNB1 and flow sorted, cell suspension was pelleted by centrifugation at 2000 x g for 3 minutes at 4°C.

Data processing

After adapter and quality trimming using Trim Galore (v0.5.0), RNAseq data was mapped to human genome GRCh38 using HISAT2 v2.1.0 by the Babraham Institute Bioinformatics Facility. Mapped data was imported into SeqMonk v1.47.0 (https://www.bioinformatics.babraham.ac.uk/projects/seqmonk/) and normalised to total read count.
Genome_build: GRCh38
tab delimited text files showing log2 values per gene for each sample

Submission date

Mar 10, 2021

Last update date

Sep 14, 2022

Contact name

Laura Biggins

E-mail(s)

laura.biggins@babraham.ac.uk

Organization name

The Babraham Institute

Department

Bioinformatics