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pmid:26981366

RNA sequencing analysis to demonstrate Erk dependent and independent functions of Mek.

Chang Liu · Haixia Chen · Lin Liu · Lingyi Chen

Genomics data · 2016 doi:10.1016/j.gdata.2015.11.029

Paper

complete

Experiment

complete

Data

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Analysis

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Execution

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RNA sequencing analysis to demonstrate Erk dependent and independent functions of Mek.
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10.1016/j.gdata.2015.11.029
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Chang Liu
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Haixia Chen
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Lin Liu
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Lingyi Chen
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Genomics data
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2016
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Mek inhibition and Erk knockout (KO) have quite distinct effects on pluripotency maintenance in mouse embryonic stem cells (ESCs). To test whether there is an Erk-independent function of Mek, RNA-sequencing (RNA-seq) is carried out on six samples, WT KH2 ESCs treated with or without PD0325901 (PD) for 48 h (KH2_PD and KH2, respectively), iErk1; Erk KO ESCs cultured in the presence of Dox (P0), 48 and 96 h after Dox withdrawal (P1 and P2, respectively), and iErk1; Erk KO ESCs cultured without Dox for 96 h, and treated with PD in the last 48 h (P2_PD). These RNA-seq data demonstrate that Mek inhibition has quite different effect on the transcriptional profile of mouse ESCs, compared to Erk KO. Moreover, a significant fraction of genes is regulated by Mek inhibition, regardless of the presence or absence of Erk, indicating an Erk-independent function of Mek. RNA-seq data are deposited in Gene Expression Omnibus (GEO) datasets under accession number GSE70304.
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RNA-seq analysis of transcriptome changes upon Erk knockout, or Mek inhibition in WT and Erk KO ESCs.
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there is an Erk-independent function of Mek, RNA-sequencing (RNA-seq) is carried out on six samples, WT
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