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Series GSE35531 Query DataSets for GSE35531
Status Public on Jan 01, 2018
Title Small RNA profiles through the cell cycle in HeLa [small RNA-seq]
Organism Homo sapiens
Experiment type Non-coding RNA profiling by high throughput sequencing
Summary Dicer plays a key role in RNA silencing. By processing pre-miRNAs and dsRNAs, Dicer generates miRNAs and siRNAs that act as post-transcriptional regulators of gene expression. Dicer is also implicated in heterochromatin formation and toxic RNA degradation. Here we report that Dicer is controlled in cell cycle. The Dicer protein level drastically rises at late G1 phase and falls at early S phase. Interestingly, the protein stability of Dicer is decreased specifically at early S phase. MG132, an inhibitor of proteasome, increases Dicer protein level, suggesting that the stability of Dicer is controlled via ubiquitination-dependent proteasome pathway.
 
Overall design All samples were first synchronized to early S phase by thymidine double block, then RNA were extracted from the cells after 8, 10, 14, 16, 18 or 20 hours from releasing the cell cycle progression.
 
Contributor(s) Lee JH, Chang H, Heo I, Park J, Kim VN
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Submission date Feb 03, 2012
Last update date May 15, 2019
Contact name Hyeshik Chang
E-mail(s) hyeshik@snu.ac.kr
Organization name Seoul National University
Department School of Biological Sciences
Lab Hyeshik Chang Lab
Street address Building 203 Room 525, School of Biological Sciences, Seoul National University, 1 Gwanak-ro, Gwanak-gu
City Seoul
State/province South Korea
ZIP/Postal code 08826
Country South Korea
 
Platforms (1)
GPL10999 Illumina Genome Analyzer IIx (Homo sapiens)
Samples (6)
GSM870233 HeLa-Thymidine-8hr
GSM870234 HeLa-Thymidine-10hr
GSM870235 HeLa-Thymidine-14hr
This SubSeries is part of SuperSeries:
GSE35533 Analysis of small RNA through the cell cycle in HeLa
Relations
SRA SRP010745
BioProject PRJNA156091

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