Cyrinne Achour

ORCID: 0000-0003-0997-5958
Publications
Citations
Views
---
Saved
---
About
Contact & Profiles
Research Areas
  • RNA modifications and cancer
  • Cancer-related gene regulation
  • RNA Research and Splicing
  • Cancer-related molecular mechanisms research
  • HVDC Systems and Fault Protection
  • RNA and protein synthesis mechanisms
  • Genomics and Chromatin Dynamics
  • Pluripotent Stem Cells Research
  • Epigenetics and DNA Methylation

Umeå University
2018-2024

National Institutes of Health
2024

National Cancer Institute
2024

Institut de Biologie Paris-Seine
2019-2020

Transgene (France)
2019-2020

Laboratoire de Biologie du Développement
2019-2020

Sorbonne Université
2019-2020

Epigénétique et Destin Cellulaire
2017

Sorbonne Paris Cité
2017

Université Paris Cité
2017

Abstract Cancer stem cells (CSCs) are a small but critical cell population for cancer biology since they display inherent resistance to standard therapies and give rise metastases. Despite accruing evidence establishing link between deregulation of epitranscriptome-related players tumorigenic process, the role messenger RNA (mRNA) modifications in regulation CSC properties remains poorly understood. Here, we show that cytoplasmic pool fat mass obesity-associated protein (FTO) impedes...

10.1038/s41467-021-21758-4 article EN cc-by Nature Communications 2021-03-19

Abstract Alternative splicing (AS) enables differential inclusion of exons from a given transcript, thereby contributing to the transcriptome and proteome diversity. Aberrant AS patterns play major roles in development different pathologies, including breast cancer. N 6 -methyladenosine (m A), most abundant internal modification eukaryotic mRNA, influences tumor progression metastasis cancer, it has been recently linked regulation. Here, we identify specific signature associated with...

10.1038/s41388-023-02602-z article EN cc-by Oncogene 2023-02-01

Abstract 2′-O-Methylation (Nm) represents one of the most common RNA modifications. Nm affects structure and function with crucial roles in various RNA-mediated processes ranging from silencing, translation, self versus non-self recognition to viral defense mechanisms. Here, we identify two methyltransferases (Nm-MTases) Drosophila melanogaster (CG7009 CG5220) as functional orthologs yeast TRM7 human FTSJ1. Genetic knockout studies together MALDI-TOF mass spectrometry RiboMethSeq mapping...

10.1093/nar/gkaa002 article EN cc-by Nucleic Acids Research 2020-01-09

Abstract Lysine-specific histone demethylase 1 (LSD1) is a that plays critical role in epigenetic regulation by removing the methyl group from mono- and di-methylated lysine 4 on H3 (H3K4me1/2), acting as repressor of gene expression. Recently, catalytically independent functions LSD1, serving scaffold for assembling chromatin-regulator transcription factor complexes, have been identified. Herein, we show first time LSD1 interacts with chromodomain-helicase-DNA-binding protein 7 (CHD7) mouse...

10.1038/s41598-024-78920-3 article EN cc-by Scientific Reports 2024-11-18

Abstract 2’-O-methylation (Nm) represents one of the most common RNA modifications. Nm affects structure and function with crucial roles in various RNA-mediated processes ranging from silencing, translation, self versus non-self recognition to viral defense mechanisms. Here, we identify two novel methyltransferases (Nm-MTases) Drosophila melanogaster (CG7009 CG5220) as functional orthologs yeast TRM7 human FTSJ1, respectively. Genetic knockout studies together MALDI-TOF mass spectrometry...

10.1101/699934 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2019-07-11

ABSTRACT Alternative splicing (AS) enables differential inclusion of exons from a given transcript, thereby contributing to the transcriptome and proteome diversity. Aberrant AS patterns play major roles in development different pathologies, including breast cancer. N 6 -methyladenosine (m A), most abundant internal modification eukaryotic mRNA, influences tumor progression metastasis cancer, it has been recently linked regulation. Here, we identify specific signature associated with...

10.1101/2022.04.11.487899 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2022-04-11
Coming Soon ...