Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Catherine Chailleux"'
Autor:
Jérémie Fages, Catherine Chailleux, Jonathan Humbert, Suk-Min Jang, Jérémy Loehr, Jean-Philippe Lambert, Jacques Côté, Didier Trouche, Yvan Canitrot
Publikováno v:
PLoS Genetics, Vol 16, Iss 6, p e1008511 (2020)
Ribosomal DNA (rDNA) is the most transcribed genomic region and contains hundreds of tandem repeats. Maintaining these rDNA repeats as well as the level of rDNA transcription is essential for cellular homeostasis. DNA damages generated in rDNA need t
Externí odkaz:
https://doaj.org/article/0423a83cc3b04ae09e91bdd5bd3f4dec
Publikováno v:
PLoS Genetics, Vol 7, Iss 6, p e1001390 (2011)
In proliferating myoblasts, muscle specific genes are silenced by epigenetic modifications at their promoters, including histone H3K9 methylation. Derepression of the promoter of the gene encoding the myogenic factor myogenin (Myog) is key for initia
Externí odkaz:
https://doaj.org/article/a1c7046ee454414690d13b0bf65667e8
Autor:
Ayeong So, Elodie Dardillac, Ali Muhammad, Catherine Chailleux, Laura Sesma-Sanz, Sandrine Ragu, Eric Le Cam, Yvan Canitrot, Jean Yves Masson, Pauline Dupaigne, Bernard S Lopez, Josée Guirouilh-Barbat
Publikováno v:
Nucleic Acids Research
Nucleic Acids Research, 2022, 50 (5), pp.2651-2666. ⟨10.1093/nar/gkac073⟩
Nucleic Acids Research, 2022, 50 (5), pp.2651-2666. ⟨10.1093/nar/gkac073⟩
Selection of the appropriate DNA double-strand break (DSB) repair pathway is decisive for genetic stability. It is proposed to act according to two steps: 1-canonical nonhomologous end-joining (C-NHEJ) versus resection that generates single-stranded
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9063f39f571d1a49962617f0379e518d
https://doi.org/10.1093/nar/gkac073
https://doi.org/10.1093/nar/gkac073
Autor:
Sandrine Ragu, Catherine Chailleux, Yvan Canitrot, Laura Sesma Sanz, Pauline Dupaigne, Jean-Yves Masson, Bernard S. Lopez, Ali Muhammad, Eric Le Cam, Ayeong So, Josée Guirouilh-Barbat
The selection of the DNA double-strand breaks (DSBs) repair pathway is decisive for genetic stability/instability. We proposed that it acts according to two successive steps: 1-canonical non-homologous end-joining (C-NHEJ)versussingle-strand DNA (ssD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4a279ad8a7bc3721225213eb37bbd96
Autor:
Catherine Chailleux, Didier Trouche, Celine Courilleau, Alexandre Carayon, François Aymard, Gemael-Cedrick Taty-Taty, Muriel Quaranta, Yvan Canitrot
Publikováno v:
Cell Cycle. 13:399-407
In mammalian cells, DNA double-strand breaks (DSB) can be repaired by 2 main pathways, homologous recombination (HR) and non-homologous end joining (NHEJ). To give access to DNA damage to the repair machinery the chromatin structure needs to be relax
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4de20ce8147d3823fbcab6d0209a3fb9
https://doi.org/10.4161/cc.27143
https://doi.org/10.4161/cc.27143
Autor:
Yvan Canitrot, Camille Gelot, Josée Guirouilh-Barbat, Elodie Dardillac, Bernard S. Lopez, Catherine Chailleux, Tangui Le Guen
Publikováno v:
Molecular Cell
Molecular Cell, 2016, 61 (1), pp.15-26. ⟨10.1016/j.molcel.2015.11.002⟩
Molecular Cell, Elsevier, 2016, 61 (1), pp.15-26. ⟨10.1016/j.molcel.2015.11.002⟩
Molecular Cell, Cell Press, 2016, 61 (1), pp.15-26. ⟨10.1016/j.molcel.2015.11.002⟩
Molecular Cell, 2016, 61 (1), pp.15-26. ⟨10.1016/j.molcel.2015.11.002⟩
Molecular Cell, Elsevier, 2016, 61 (1), pp.15-26. ⟨10.1016/j.molcel.2015.11.002⟩
Molecular Cell, Cell Press, 2016, 61 (1), pp.15-26. ⟨10.1016/j.molcel.2015.11.002⟩
The end joining of distant DNA double-strand ends (DSEs) can produce potentially deleterious rearrangements. We show that depletion of cohesion complex proteins specifically stimulates the end joining (both C-NHEJ and A-EJ) of distant, but not close,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29fe1e1779dfe0bf3a27700db8e105f1
https://hal.science/hal-03048245
https://hal.science/hal-03048245
Autor:
Hélène Richard-Foy, Didier Trouche, Mathide Calligé, Philippe Rochaix, Catherine Chailleux, Claire Giamarchi
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 1578:12-20
We show here that the two antagonists ICI 182 780, a pure estrogen antagonist, and 4-hydroxy-tamoxifen, a selective estrogen receptor modulator (SERM) have distinct effects on TFF1 (formerly pS2) gene chromatin structure and transcription. Indeed, IC
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76a3504b96c0f6d5503c6b6ab335dd4b
https://doi.org/10.1016/s0167-4781(02)00480-3
https://doi.org/10.1016/s0167-4781(02)00480-3
Autor:
Yvan Canitrot, Virginie Daburon, Pierre Caron, Céline Courilleau, François Aymard, Gaëlle Legube, Didier Trouche, Catherine Chailleux
Publikováno v:
Nature Protocols
Nature Protocols, Nature Publishing Group, 2014, 9 (3), pp.517-528. ⟨10.1038/nprot.2014.031⟩
Nature Protocols, Nature Publishing Group, 2014, 9 (3), pp.517-528. ⟨10.1038/nprot.2014.031⟩
Recent advances in our understanding of the management and repair of DNA double-strand breaks (DSBs) rely on the study of targeted DSBs that have been induced in living cells by the controlled activity of site-specific endonucleases, usually recombin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e288081baec82fbd4ac11332cf35bb55
https://pubmed.ncbi.nlm.nih.gov/24504477
https://pubmed.ncbi.nlm.nih.gov/24504477
Autor:
Sandrine Tyteca, Yvan Canitrot, Catherine Chailleux, Nadine Puget, Céline Courilleau, François Boudsocq, Didier Trouche, Christophe Papin, Mikhail Grigoriev
Publikováno v:
Biochemical Journal
Biochemical Journal, Portland Press, 2010, 426 (3), pp.365-371. ⟨10.1042/BJ20091329⟩
Biochemical Journal, Portland Press, 2010, 426 (3), pp.365-371. ⟨10.1042/BJ20091329⟩
Chromatin modifications and chromatin-modifying enzymes are believed to play a major role in the process of DNA repair. The histone acetyl transferase Tip60 is physically recruited to DNA DSBs (double-strand breaks) where it mediates histone acetylat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc42cd475063a2a5a9a454d6f32cac5c
https://hal.archives-ouvertes.fr/hal-00479248/file/PEER_stage2_10.1042%2FBJ20091329.pdf
https://hal.archives-ouvertes.fr/hal-00479248/file/PEER_stage2_10.1042%2FBJ20091329.pdf
Publikováno v:
Molecular Cancer Research
Molecular Cancer Research, American Association for Cancer Research, 2008, 6 (3), pp.418-25. ⟨10.1158/1541-7786.MCR-07-0381⟩
Molecular Cancer Research, American Association for Cancer Research, 2008, 6 (3), pp.418-25. ⟨10.1158/1541-7786.MCR-07-0381⟩
Permanent silencing of E2F-dependent genes is a hallmark of the irreversible cell cycle exit that characterizes terminally differentiated and senescent cells. The determinant of this silencing during senescence has been proposed to be the binding of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a85a99ec396c1715720cf3ddd794d44a
https://hal.archives-ouvertes.fr/hal-00317872
https://hal.archives-ouvertes.fr/hal-00317872