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SRX5141903: GSM3517733: Synchronized RNA-seq_Control_time_8; Homo sapiens; RNA-Seq
1 ILLUMINA (HiSeq X Ten) run: 35.1M spots, 10.6G bases, 3.8Gb downloads

Submitted by: NCBI (GEO)
Study: RNA-binding chromatin modifier MTA1 regulates mitotic transition and tumorigenesis by orchestrating mitotic mRNA processing [Synchronized RNA-seq]
show Abstracthide Abstract
The processing of RNAs by chromatin-associated proteins (CAPs) is highlighted by the latest findings. However, whether and how CAP-RNA interactions regulate cancer biology remain underdefined. Using modified fCLIP-seq technology, we show that, cancer metastasis-associated antigen 1 (MTA1), a well-known oncogenic chromatin modifier, binds bulk transcripts, preferentially at splicing-responsible motifs, influencing the abundance and alternative splicing (AS) of target transcripts, preferentially those encoding mitosis regulators. MTA1 orchestrates the fluctuant pre-mRNA AS kinetics of mitosis regulators, such as ATRX and MYBL2, during mitosis. MTA1 overexpression causes a defective mitotic arrest, leading to aberrant chromosome segregation, and CIN occurrence in cancer cells and clinical tumors, which eventually contributes to tumorigenesis. Hence, we present MTA1 as a pivotal RNA-binding CAP linked to mitosis control in tumorigenesis. Overall design: RNA-seq experiments performed on MTA1-knockout and control samples from synchronized HCT116 cells. Each was performed with three replicates.
Sample: Synchronized RNA-seq_Control_time_8
SAMN10603306 • SRS4152531 • All experiments • All runs
Organism: Homo sapiens
Library:
Instrument: HiSeq X Ten
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: RNA was harvested using Trizol reagent.Total RNA was treated with RQ1 DNase (promega) to remove DNA. The quality and quantity of the purified RNA were determined by measuring the absorbance at 260nm/280nm (A260/A280) using smartspec plus (BioRad). RNA integrity was further verified by 1.5% Agarose gel electrophoresis. RNA libraries were prepared for sequencing using standard Illumina protocols
Experiment attributes:
GEO Accession: GSM3517733
Links:
Runs: 1 run, 35.1M spots, 10.6G bases, 3.8Gb
Run# of Spots# of BasesSizePublished
SRR833034235,076,48410.6G3.8Gb2020-07-18

ID:
6956398

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