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Trincr1 RNA pull down MS in mESC

ABSTRACT: Long noncoding RNAs (lncRNAs) have emerged as important components of gene regulatory network in embryonic stem cells (ESCs). However, the function and molecular mechanism of lncRNAs are still largely unknown. Here we identified Trincr1 (TRIM71 interacting long noncoding RNA 1) lncRNA that regulates the FGF/ERK signaling and self-renewal of ESCs. Trincr1 is exported by THOC complex to cytoplasm where it binds and represses TRIM71, leading to the downregulation of SHCBP1 protein. Knocking out Trincr1 leads to the upregulation of phosphorylated ERK and ERK pathway target genes and the decrease of ESC self-renewal, while knocking down Trim71 completely rescues the defects of Trincr1 knockout. Furthermore, ectopic expression of Trincr1 represses FGF/ERK signaling and the self-renewal of neural progenitor cells. Together, this study reveals more regulators in FGF/ERK signaling pathway and highlights lncRNA as an important player in cell signaling network to coordinate cell fate specification.

INSTRUMENT(S): LTQ Orbitrap Elite

ORGANISM(S): Mus Musculus (mouse)

TISSUE(S): Cell Culture, Embryonic Stem Cell

SUBMITTER: Yangming Wang

LAB HEAD: Yangming Wang

PROVIDER: PXD012493 | Pride | 2019-02-01

REPOSITORIES: Pride

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			Action	DRS
	16-093_LYP0329_case.raw	Raw
	16-093_LYP0329_case_pep.csv	Csv
	16-093_LYP0329_case_pro.csv	Csv
	16-093_LYP0329_control.raw	Raw
	16-093_LYP0329_control_pep.csv	Csv

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