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SRX684306: GSM1482896: Int11 replicat3; Homo sapiens; RNA-Seq
1 ILLUMINA (Illumina HiSeq 2000) run: 59.2M spots, 3G bases, 1.8Gb downloads

Submitted by: Gene Expression Omnibus (GEO)
Study: Integrator complex regulates NELF-mediated RNA Polymerase II pause/release and processivity at coding genes [RNA-seq]
show Abstracthide Abstract
RNAPII pausing/termination shortly after initiation is a hallmark of gene regulation. However, the molecular mechanisms involved are still to be uncovered. Here, we show that NELF interacts with Integrator complex subunits (INTScom) forming a stable complex with RNPII and Spt5. The interaction between NELF and INTScom subunits is RNA and DNA independent. Using both HIV-1 promoter and genome wide analyses, we demonstrate that Integrator subunits specifically control NELF-mediated RNAPII pause/release at coding genes. The strength of RNAPII pausing is determined by the nature of the NELF-associated complex. Interestingly, in addition to controlling RNAPII pause release INTS11 catalytic subunit of the INTScom is required for the synthesis of full length mRNA. Finally, INTScom-target genes are enriched in HIV-1 TAR/ NELF-binding element and in a 3'box sequence required for snRNA biogenesis. Revealing these unexpected functions of INTScom in regulating RNAPII pausing/release and completion of mRNA synthesis of NELF-target genes will contribute to our understanding of the gene expression cycle. Overall design: Genome-wide expression in HeLa cells in the absence of Integrator 11, or NELF or mock (control) depleted by strand-specific RNASeq (Illumina)
Sample: Int11 replicat3
SAMN03000063 • SRS687433 • All experiments • All runs
Organism: Homo sapiens
Library:
Instrument: Illumina HiSeq 2000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: SINGLE
Construction protocol: Total RNAs whole-cell RNAs were depleted for ribosomal RNAs using the Ribo-ZeroTM Magnetic Gold Kit following manufacturer’s instructions.For total RNA samples (siInt11_1/2/3, SiNELF-1/2-3; Siscrambled-1/2/3), 100 ng of ribosomal RNA depleted whole cell RNA was used for library construction following Illumina’s instructions. cDNA libraries of poly-adenylated RNAs ('Int11-1/2-3' NELF-1/2/3; scr/Scrambled-1/2/3) were generated using 1 µg of whole-cell RNAs following Illumina’s instructions. Librairies were prepared using Illumina Tru-Seq stranded mRNA sample prep kit TruSeq Sample Prep Kit (multiplexed libraries) according to manufacturer’s instructions.(Illumina).
Experiment attributes:
GEO Accession: GSM1482896
Links:
External link:
Runs: 1 run, 59.2M spots, 3G bases, 1.8Gb
Run# of Spots# of BasesSizePublished
SRR155515459,194,6213G1.8Gb2015-05-19

ID:
958131

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