U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

SRX2208964: GSM2334826: RNA-seq RPMI-8226 Rep1; Homo sapiens; RNA-Seq
1 ILLUMINA (Illumina HiSeq 2500) run: 17.4M spots, 4.4G bases, 2Gb downloads

Submitted by: NCBI (GEO)
Study: 3D genome of multiple myeloma reveals spatial genome disorganization associated with copy number variations
show Abstracthide Abstract
Hi-C technique has been widely applied to study the three-dimensional architecture of the whole genome. Genome structures such as compartment A/B, TAD (topologically associated domain) and chromatin loops can be identified from Hi-C data in both normal cells of human and other species, and are found to be associated with features such as epigenetic markers, DNA-binding proteins and gene expression. But such technique had been rarely used in cancer studies. Here we used Hi-C to study the aneuploid cancer genomic architecture in multiple myeloma cells. Our results indicate that Hi-C interaction matrix of cancer cells is affected by CNVs and should be adjusted for copy number. After correcting this CNV bias, we found a significant overlapping between the boundaries of CNV blocks and boundaries of TADs, which suggests that TAD boundaries are fragile sites for CNV breakpoints. In addition, the compartment A/B switching is associated with differential gene expression, from which we found important genes that are related with multiple myeloma. We build a 3D structure model of the aneuploidy genome and found that there are great changes both in the whole genome spatial interactome and local chromosome territories. In summary, our research builds the first 3D genome interaction maps of multiple myeloma and the first time notice this CNV-driven bias in Hi-C studies, which may deepen our understanding of changes in cancer 3D genome. Overall design: Integrated analysis of 3D genome architecture, gene expression, and genome structure variations in multiple myelomas.
Sample: RNA-seq RPMI-8226 Rep1
SAMN05860229 • SRS1726326 • All experiments • All runs
Organism: Homo sapiens
Library:
Instrument: Illumina HiSeq 2500
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Total RNA was collected using the TRIzol® Reagent (Life Technologies) following the manufacturer's instructions. mRNA was purified from total RNA using poly-T oligo-attached magnetic beads. Fragmentation was carried out using divalent cations under elevated temperature in NEBNext First Strand Synthesis Reaction Buffer (5X). First strand cDNA was synthesized using random hexamer primer and M-MuLV Reverse Transcriptase (RNaseH-). Second strand cDNA synthesis was subsequently performed using DNA Polymerase I and RNase H. Remaining overhangs were converted into blunt ends via exonuclease/polymerase activities. After adenylation of 3' ends of DNA fragments, NEBNext Adaptor with hairpin loop structure was ligated to prepare for hybridization. In order to select cDNA fragments with right length, the library fragments were purified with AMPure XP system (Beckman Coulter, Beverly, USA). Then, 3 μl USER Enzyme (NEB, USA) was used with size-selected, adaptor-ligated cDNA at 37°C for 15 min followed by 5 min at 95°C before PCR. Then, PCR was performed with Phusion High-Fidelity DNA polymerase, Universal PCR primers and Index (X) Primer. At last, products were purified (AMPure XP system) and library quality was assessed on the Agilent Bioanalyzer 2100 system.
Experiment attributes:
GEO Accession: GSM2334826
Links:
Runs: 1 run, 17.4M spots, 4.4G bases, 2Gb
Run# of Spots# of BasesSizePublished
SRR434189517,418,5674.4G2Gb2017-11-21

ID:
3244456

Supplemental Content

Search details

See more...

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...