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Multiple regulators mediate the transcriptional activities of ERRalpha and its capacity to promote cell invasion

Date
mer 05 sep 2018
Horaires

9h00

Lieu(x)
East China Normal University

Shanghai - RP CHINE

Intervenant(s)

Soutenance de thèse de Mlle Ling ZHANG de l'IGFL sous la direction de M. Jean-Marc VANACKER et sous la cotutelle de M.Jiemin WONG (ECNU)

Langue(s) des interventions

Description générale

ERRa   is a nuclear receptor whose activity mainly depends on its interaction with transcription co-regulators. High levels of ERRa  are found in various cancer types and correlate with poor prognosis. However, the mechanisms linking ERRα to cancer cell migration as well as the coregulators involved are unclear. In our study, we found two histone-modifying enzymes, LSD1 and SET7, acting as positive regulators of ERRα.
I. ERRa impacts the biochemical activities of the LSD1 demethylase. Activation of ERRa -LSD1 targets (identified by RNA-Seq) requires the recruitment of this complex at Transcriptional Start Sites (TSSs), which is achieved by the NRF1 transcription factor. In our study, we have shown several points: NRF1, but not ERRa , is involved in positioning LSD1 to TSS, whereas ERRa , but not NRF1, regulates LSD1 enzymatic activities towards demethylating H3K9me2.
II. A distinct group of ERRa  target genes (identified by RNA-Seq) is under the control of the histone methyltransferase SET7 which mono-methylates H3K4. Appropriate recruitment of SET7 at TSSs is controlled by the ETS1 transcription factor, promoting the interaction between SET7-ERRa , leading to target gene expression.
Gene Ontology analysis revealed that ERRa -LSD1 co-targets, as well as ERRa -SET7 co-targets, are enriched in terms of cell invasion. Consistently, depletion of each of these factors, as well as depletion of NRF1 or ETS1, leads to reduced cell invasion capacities as observed in transwell assays or in vivo, using xenotransplantation in the zebrafish embryo.
Altogether, our results show two regulatory networks involving histone modifications induced by nuclear receptors, leading to increased cell invasion.

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