Unknown,Transcriptomics,Genomics,Proteomics

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Genome-wide analysis of mRNAs expression in prometaphase


ABSTRACT: The goal of this experiment was to compare the transcriptome of cells that overexpressed the RNA-binding protein Staufen1 to that of cells that expressed the empty vector as control. Stau1 abundance fluctuates through the cell cycle: it is high in the G2 phase of the cell cycle and rapidly decreases as cells transit through mitosis. The importance of controlling Stau1 levels was underscored by the observation that its overexpression impairs mitosis as well as proliferation of transformed cell lines. As a major post-transcriptional regulator, Stau1 may exert its role(s) through the spatial and/or temporal regulation of its bound mRNAs. Therefore, to gather clues to support this possibility, we determined if Stau1 overexpression significantly modified the transcriptome of transformed cells in prometaphase explaining the observed impairment in mitosis transit and/or cell proliferation. HEK293T cells were transfected with plasmids coding for Stau155-FLAG or the empty vector as control. Cells were synchronized in prometaphase with nocodazole.

ORGANISM(S): Homo sapiens

SUBMITTER: Luc DesGroseillers 

PROVIDER: E-GEOD-51182 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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Publications

Cell cycle-dependent regulation of the RNA-binding protein Staufen1.

Boulay Karine K   Ghram Mehdi M   Viranaicken Wildriss W   Trépanier Véronique V   Mollet Stéphanie S   Fréchina Céline C   DesGroseillers Luc L  

Nucleic acids research 20140606 12


Staufen1 (Stau1) is a ribonucleic acid (RNA)-binding protein involved in the post-transcriptional regulation of gene expression. Recent studies indicate that Stau1-bound messenger RNAs (mRNAs) mainly code for proteins involved in transcription and cell cycle control. Consistently, we report here that Stau1 abundance fluctuates through the cell cycle in HCT116 and U2OS cells: it is high from the S phase to the onset of mitosis and rapidly decreases as cells transit through mitosis. Stau1 down-reg  ...[more]

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