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SRX2779455: GSM2597310: SRpP55 KD (siSR#2) exposed 1; Homo sapiens; RNA-Seq
17 ILLUMINA (Illumina HiSeq 2000) runs: 67M spots, 13.5G bases, 9Gb downloads

Submitted by: NCBI (GEO)
Study: A SRp55-regulated alternative splicing network controls pancreatic beta cell survival and function
show Abstracthide Abstract
Progressive failure of insulin-producing beta cells is the central event leading to diabetes, yet the signalling networks controlling beta cell fate remain poorly understood. Here we show that SRp55, a splicing factor regulated by the diabetes susceptibility gene GLIS3, has a major role in maintaining function and survival of human beta cells. RNA-seq analysis revealed that SRp55 regulates the splicing of genes involved in cell survival and death, insulin secretion and JNK signalling. Specifically, SRp55-mediated splicing changes modulate the function of the pro-apoptotic proteins BIM and BAX, JNK signalling and endoplasmic reticulum stress, explaining why SRp55 depletion triggers beta cell apoptosis. Furthermore, SRp55 depletion inhibits beta cell mitochondrial function, explaining the observed decrease in insulin release. These data unveil a novel layer of regulation of human beta cell function and survival, namely alternative splicing modulated by key splicing regulators such as SRp55 that may crosstalk with candidate genes for diabetes. Overall design: Five independent preparations of EndoC-ßH1 cells exposed to control (siCTL) or SRp55 (siSR#2) siRNAs
Sample: SRpP55 KD (siSR#2) exposed 1
SAMN06883697 • SRS2162704 • All experiments • All runs
Organism: Homo sapiens
Library:
Instrument: Illumina HiSeq 2000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Total RNA was isolated from Maria using the RNeasy Mini kit (Qiagen, Venlo, The Netherlands) which favours purification of RNA molecules longer than 200 nucleotides. mRNA was purified from 1 μg total RNA using oligo (dT) beads, before it was fragmented and randomly primed for reverse transcription followed by second-strand synthesis to create ds cDNA fragments. mRNA was purified from 1 µg total RNA using oligo (dT) beads, before it was fragmented and randomly primed for reverse transcription followed by second-strand synthesis to create ds cDNA fragments. The generated cDNA had undergone paired-end repair to convert overhangs into blunt ends. After 39- monoadenylation and adaptor ligation, cDNAs were purified on a 2% agarose gel and 200 basepair (bp) products were excised from the gel. Following gel digestion, purified cDNA was amplified by PCR using primers specific for the ligated adaptors. The generated libraries were submitted to quality control with the Agilent bio- analyzer 2100 (Agilent Technologies, Wokingham, UK) before sequencing. The RNA integrity number (RIN) values for all samples were 7.5 and above. 1 µl cDNA was loaded on an Agilent DNA chip (DNA-1000) to verify cDNA quality and quantity. Only libraries reaching satisfactory conditions were used for sequencing, on an Illumina HiSeq 2000 system
Experiment attributes:
GEO Accession: GSM2597310
Links:
Runs: 17 runs, 67M spots, 13.5G bases, 9Gb
Run# of Spots# of BasesSizePublished
SRR54992364,000,000808M532.3Mb2018-02-05
SRR54992374,000,000808M533.1Mb2018-02-05
SRR54992384,000,000808M550.4Mb2018-02-05
SRR54992394,000,000808M543.6Mb2018-02-05
SRR54992404,000,000808M538.6Mb2018-02-05
SRR54992414,000,000808M560.5Mb2018-02-05
SRR54992424,000,000808M534.4Mb2018-02-05
SRR54992434,000,000808M545.6Mb2018-02-05
SRR54992443,026,888611.4M430.4Mb2018-02-05
SRR54992454,000,000808M545.8Mb2018-02-05
SRR54992464,000,000808M564.1Mb2018-02-05
SRR54992474,000,000808M538.3Mb2018-02-05
SRR54992484,000,000808M548.4Mb2018-02-05
SRR54992494,000,000808M562.1Mb2018-02-05
SRR54992504,000,000808M538.4Mb2018-02-05
There are 2 omitted runs. See all runs in Run Selector.

ID:
4007460

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