C. Francastel

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Coding and Non-coding RNAs, the Frontier Has Never Been So Blurred

F. Hubé, C. Francastel, 2018, Front. Genet..

Corrigendum: Mutations in CDCA7 and HELLS cause immunodeficiency–centromeric instability–facial anomalies syndrome

Yuya Ito, Jun Wang, Mikita Suyama, 2016, Nature Communications.

When one is better than two: RNA with dual functions.

Claire Francastel, F. Hubé, C. Francastel, 2011, Biochimie.

Mammalian Introns: When the Junk Generates Molecular Diversity

F. Hubé, C. Francastel, 2015, International journal of molecular sciences.

DNA methylation in satellite repeats disorders.

F. Magdinier, C. Francastel, 2019, Essays in biochemistry.

Comparative methylome analysis of ICF patients identifies heterochromatin loci that require ZBTB24, CDCA7 and HELLS for their methylated state

Laure Ferry, C. Picard, J. Deleuze, 2018, Human molecular genetics.

Multiple information carried by RNAs: total eclipse or a light at the end of the tunnel?

F. Hubé, C. Francastel, Baptiste Bogard, 2020, RNA biology.

Nuclear relocation of a transactivator subunit precedes target gene activation

M. Groudine, C. Francastel, W. Magis, 2001, Proceedings of the National Academy of Sciences of the United States of America.

Three novel ZBTB24 mutations identified in Japanese and Cape Verdean type 2 ICF syndrome patients

C. Picard, M. Unoki, H. Sasaki, 2013, Journal of Human Genetics.

Regulation of telomeric function by DNA methylation differs between humans and mice.

S. Selig, L. Godley, C. Francastel, 2020, Human molecular genetics.

CDCA7 and HELLS suppress DNA:RNA hybrid-associated DNA damage at pericentromeric repeats

H. Sasaki, H. Koseki, Yuichiro Saito, 2020, Scientific Reports.

Genetic, Cellular and Clinical Features of ICF Syndrome: a French National Survey

A. Fischer, C. Picard, N. Mahlaoui, 2016, Journal of Clinical Immunology.

Germline genes hypomethylation and expression define a molecular signature in peripheral blood of ICF patients: implications for diagnosis and etiology

C. Picard, A. Mégarbané, H. Sasaki, 2014, Orphanet Journal of Rare Diseases.

MafG Sumoylation Is Required for Active Transcriptional Repression

J. D. Engel, J. Engel, Masayuki Yamamoto, 2006, Molecular and Cellular Biology.

Identification of a dinucleotide signature that discriminates coding from non-coding long RNAs

M. Dinger, F. Hubé, C. Francastel, 2014, Front. Genet..

Upregulation of CD9 expression during TPA treatment of K562 cells

O. Lantz, C. Boucheix, E. Rubinstein, 1997, Leukemia.

A new method for the identification of thousands of circular RNAs

F. Hubé, C. Francastel, Baptiste Bogard, 2018 .

Preferential association of irreversibly silenced E2F-target genes with pericentromeric heterochromatin in differentiated muscle cells

A. Harel-Bellan, L. Fritsch, L. Pritchard, 2010, Epigenetics.

Nuclear compartmentalization and gene activity

Dirk Schübeler, Mark Groudine, Claire Francastel, 2000, Nature Reviews Molecular Cell Biology.

A Functional Enhancer Suppresses Silencing of a Transgene and Prevents Its Localization Close to Centromeric Heterochromatin

Mark Groudine, Claire Francastel, David I. K. Martin, 1999, Cell.

Maintenance of DNA methylation: Dnmt3b joins the dance

C. Francastel, G. Velasco, E. Walton, 2011, Epigenetics.

Short intron-derived ncRNAs

A. Sureau, F. Hubé, C. Francastel, 2017, Nucleic acids research.

Steroid receptor RNA activator protein binds to and counteracts SRA RNA-mediated activation of MyoD and muscle differentiation

Florent Hubé, Guillaume Velasco, Jérôme Rollin, 2010, Nucleic Acids Res..

Dnmt3b recruitment through E2F6 transcriptional repressor mediates germ-line gene silencing in murine somatic tissues

Damien Neuillet, E. Viégas-Péquignot, F. Hubé, 2010, Proceedings of the National Academy of Sciences.

ICF-specific DNMT3B dysfunction interferes with intragenic regulation of mRNA transcription and alternative splicing

M. D'Esposito, C. Angelini, M. Gagliardi, 2017, Nucleic acids research.

Interplay between Histone and DNA Methylation Seen through Comparative Methylomes in Rare Mendelian Disorders

V. Cormier-Daire, C. Francastel, G. Velasco, 2021, International journal of molecular sciences.

CDCA7 and HELLS mutations undermine nonhomologous end joining in centromeric instability syndrome

H. Sasaki, C. Francastel, H. Funabiki, 2018, The Journal of clinical investigation.

Dnmt3b Prefers Germ Line Genes and Centromeric Regions: Lessons from the ICF Syndrome and Cancer and Implications for Diseases

C. Francastel, G. Velasco, E. Walton, 2014, Biology.

Long-Distance Control of Origin Choice and Replication Timing in the Human β-Globin Locus Are Independent of the Locus Control Region

M. Groudine, D. Schübeler, A. Reik, 2000, Molecular and Cellular Biology.

Genetics meets DNA methylation in rare diseases

C. Francastel, G. Velasco, Guillaume Velasco, 2019, Clinical genetics.

Contrasting epigenetic states of heterochromatin in the different types of mouse pluripotent stem cells

Giacomo Grillo, V. Brochard, A. Jouneau, 2018, Scientific Reports.

Accumulation of small murine minor satellite transcripts leads to impaired centromeric architecture and function.

C. Francastel, A. Guais, H. Bouzinba-Ségard, 2006, Proceedings of the National Academy of Sciences of the United States of America.

Chromatin Modifications in Hematopoietic Multipotent and Committed Progenitors Are Independent of Gene Subnuclear Positioning Relative to Repressive Compartments

Marta Maleszewska, C. Francastel, M. Rouyez, 2009, Stem cells.

Subtelomeric methylation distinguishes between subtypes of Immunodeficiency, Centromeric instability and Facial anomalies syndrome

S. Selig, A. Kaindl, C. Francastel, 2018, Human molecular genetics.

Evaluation of DNA Methylation Episignatures for Diagnosis and Phenotype Correlations in 42 Mendelian Neurodevelopmental Disorders.

M. Shaw, N. de Leeuw, J. Gécz, 2020, American journal of human genetics.

Systematic Identification and Functional Validation of New snoRNAs in Human Muscle Progenitors

F. Hubé, C. Francastel, Baptiste Bogard, 2021, Non-coding RNA.

BRCA1 prevents R-loop-associated centromeric instability

C. Francastel, P. Calsou, S. Britton, 2021, Cell Death & Disease.

Centromeres Transcription and Transcripts for Better and for Worse.

C. Francastel, Sabrine Hédouin, Pia Mihìc, 2021, Progress in molecular and subcellular biology.

Genetic, Cellular and Clinical Features of ICF Syndrome: a French National Survey

A. Fischer, C. Picard, N. Mahlaoui, 2016, Journal of Clinical Immunology.

Evaluation of DNA Methylation Episignatures for Diagnosis and Phenotype Correlations in 42 Mendelian Neurodevelopmental Disorders.

M. Shaw, N. de Leeuw, J. Gécz, 2021, American journal of human genetics.

Mutations in CDCA7 and HELLS cause immunodeficiency–centromeric instability–facial anomalies syndrome

M. Suyama, C. Picard, A. Gennery, 2015, Nature Communications.

Nuclear localization and histone acetylation: a pathway for chromatin opening and transcriptional activation of the human beta-globin locus.

M. Groudine, D. Schübeler, A. Reik, 2000, Genes & development.

Lymphoid-affiliated genes are associated with active histone modifications in human hematopoietic stem cells.

M. Cavazzana‐Calvo, D. Charron, Marta Maleszewska, 2008, Blood.

Coding or non-coding: Need they be exclusive?

F. Hubé, C. Francastel, 2011, Biochimie.

Identification of potentially new bifunctional RNA based on genome-wide data-mining of alternative splicing events.

Claire Francastel, F. Hubé, C. Francastel, 2011, Biochimie.

Telomeres in ICF syndrome cells are vulnerable to DNA damage due to elevated DNA:RNA hybrids

F. Chédin, S. Selig, C. Francastel, 2017, Nature Communications.

Non-coding murine centromeric transcripts associate with and potentiate Aurora B kinase

F. Hubé, C. Francastel, G. Velasco, 2009, Nucleic acids research.

Dynamic changes in transcription factor complexes during erythroid differentiation revealed by quantitative proteomics

R. Aebersold, G. Crabtree, M. Brand, 2004, Nature Structural &Molecular Biology.

CENP-A chromatin disassembly in stressed and senescent murine cells

Giacomo Grillo, C. Francastel, I. Ivkovic, 2017, Scientific Reports.

NF-E2p18/mafK is required in DMSO-induced differentiation of Friend erythroleukemia cells by enhancing NF-E2 activity

C. Francastel, J. Robert-Lézénès, Y. Augery-Bourget, 1997, Leukemia.

Antisense c-jun overcomes a differentiation block in a murine erythroleukemia cell line.

R. Groisman, C. Francastel, C. Pfarr, 1994, Oncogene.

Co-induction of c-fos and junB during the latent period preceding commitment of Friend erythroleukemia cells to differentiation.

C. Francastel, J. Robert-Lézénès, Z. Mazouzi, 1992, Leukemia.

Tunable DNMT1 degradation reveals cooperation of DNMT1 and DNMT3B in regulating DNA methylation dynamics and genome organization

L. Mirny, Nezar Abdennur, F. Foijer, 2023, bioRxiv.

The Non-Coding RNA Journal Club: Highlights on Recent Papers—3

G. Calin, I. Berindan‐Neagoe, G. Santulli, 2015, Non-Coding RNA.

“Pocket-sized RNA-Seq”: A Method to Capture New Mature microRNA Produced from a Genomic Region of Interest

F. Hubé, C. Francastel, 2015, Non-coding RNA.

Proteasome inhibition alters mitotic progression through the upregulation of centromeric α‐Satellite RNAs

J. Shetty, Bao Tran, D. Prada, 2021, The FEBS journal.

Identification of potentially new bifunctional RNA based on genome-wide data-mining of alternative splicing events.

F. Hubé, C. Francastel, D. Ulveling, 2011, Biochimie.

Proteasome inhibition alters mitotic progression through the upregulation of centromeric -Satellite RNAs