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Epitranscriptomics & Cancer Adaptation : A.David

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Our research work focuses on the contribution of post-transcriptional mechanisms on cancer cell adaptation, in particular RNA epigenetic & translational control.

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Group name EQUIPEFC
Item Type Journal Article
Title In mammalian foetal testes, SOX9 regulates expression of its target genes by binding to genomic regions with conserved signatures
Creator Rahmoun et al.
Author Massilva Rahmoun
Author Rowena Lavery
Author Sabine Laurent-Chaballier
Author Nicolas Bellora
Author Gayle K. Philip
Author Moïra Rossitto
Author Aleisha Symon
Author Eric Pailhoux
Author Florence Cammas
Author Jessica Chung
Author Stefan Bagheri-Fam
Author Mark Murphy
Author Vivian Bardwell
Author David Zarkower
Author Brigitte Boizet-Bonhoure
Author Philippe Clair
Author Vincent R. Harley
Author Francis Poulat
Abstract In mammalian embryonic gonads, SOX9 is required for the determination of Sertoli cells that orchestrate testis morphogenesis. To identify genetic networks directly regulated by SOX9, we combined analysis of SOX9-bound chromatin regions from murine and bovine foetal testes with sequencing of RNA samples from mouse testes lacking Sox9. We found that SOX9 controls a conserved genetic programme that involves most of the sex-determining genes. In foetal testes, SOX9 modulates both transcription and directly or indirectly sex-specific differential splicing of its target genes through binding to genomic regions with sequence motifs that are conserved among mammals and that we called 'Sertoli Cell Signature' (SCS). The SCS is characterized by a precise organization of binding motifs for the Sertoli cell reprogramming factors SOX9, GATA4 and DMRT1. As SOX9 biological role in mammalian gonads is to determine Sertoli cells, we correlated this genomic signature with the presence of SOX9 on chromatin in foetal testes, therefore equating this signature to a genomic bar code of the fate of foetal Sertoli cells. Starting from the hypothesis that nuclear factors that bind to genomic regions with SCS could functionally interact with SOX9, we identified TRIM28 as a new SOX9 partner in foetal testes.
Publication Nucleic Acids Research
Volume 45
Issue 12
Pages 7191-7211
Date Jul 07, 2017
Journal Abbr Nucleic Acids Res.
Language eng
DOI 10.1093/nar/gkx328
ISSN 1362-4962
Library Catalog PubMed
Extra PMID: 28472341 PMCID: PMC5499551
Tags Animals, Cattle, Chromatin, Embryo, Mammalian, Female, Fetus, GATA4 Transcription Factor, Gene Expression Regulation, Developmental, Gene Regulatory Networks, Male, Mice, Morphogenesis, Nuclear Proteins, Protein Binding, Repressor Proteins, Sequence Analysis, RNA, Sertoli Cells, Sex Determination Processes, SOX9 Transcription Factor, Transcription Factors, Transcriptome, Tripartite Motif-Containing Protein 28
Date Added 2019/12/19 - 15:59:09
Date Modified 2019/12/19 - 15:59:09
Notes and Attachments PubMed entry (Attachment)
Texte intégral (Attachment)


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