Zobrazeno 1 - 10
of 68
pro vyhledávání: '"MESH: DNA Breaks"'
Autor:
Alexandre Nore, Ariadna B. Juarez-Martinez, Julie Clément, Christine Brun, Boubou Diagouraga, Hamida Laroussi, Corinne Grey, Henri Marc Bourbon, Jan Kadlec, Thomas Robert, Bernard de Massy
Publikováno v:
Nature Communications
Nature Communications, 2022, 13 (1), pp.7048. ⟨10.1038/s41467-022-34799-0⟩
Nature Communications, 2022, 13 (1), pp.7048. ⟨10.1038/s41467-022-34799-0⟩
Meiosis requires the formation of programmed DNA double strand breaks (DSBs), essential for fertility and for generating genetic diversity. In male and female meiotic cells, DSBs are induced by the catalytic activity of the TOPOVIL complex formed by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a32a901d169c80386cfd45a59ed2c889
https://hal.science/hal-03853094
https://hal.science/hal-03853094
Autor:
Estelle Vincendeau, Wenming Wei, Xuefei Zhang, Cyril Planchais, Wei Yu, Hélène Lenden-Hasse, Thomas Cokelaer, Juliana Pipoli da Fonseca, Hugo Mouquet, David J. Adams, Frederick W. Alt, Stephen P. Jackson, Gabriel Balmus, Chloé Lescale, Ludovic Deriano
Publikováno v:
Nature Communications
Nature Communications, 2022, 13 (1), pp.3707. ⟨10.1038/s41467-022-31287-3⟩
Nature Communications, 2022, 13 (1), pp.3707. ⟨10.1038/s41467-022-31287-3⟩
Funder: Ligue Nationale Contre le Cancer
SHLD1 is part of the Shieldin (SHLD) complex, which acts downstream of 53BP1 to counteract DNA double-strand break (DSB) end resection and promote DNA repair via non-homologous end-joining (NHEJ). While 5
SHLD1 is part of the Shieldin (SHLD) complex, which acts downstream of 53BP1 to counteract DNA double-strand break (DSB) end resection and promote DNA repair via non-homologous end-joining (NHEJ). While 5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6552ddce6e8fcc03619460c08b3e7d7a
Autor:
Murielle Chauvel, Adeline Feri, Corinne Maufrais, Mélanie Legrand, Christophe d'Enfert, Timea Marton
Publikováno v:
Genetics
Genetics, 2021, 218 (1), pp.iyab028. ⟨10.1093/genetics/iyab028⟩
Genetics, 2021, 218 (1), pp.iyab028. ⟨10.1093/genetics/iyab028⟩
Genomic rearrangements have been associated with the acquisition of adaptive phenotypes, allowing organisms to efficiently generate new favorable genetic combinations. The diploid genome of Candida albicans is highly plastic, displaying numerous geno
Autor:
de Krijger, Inge, Föhr, Bastian, Pérez, Santiago Hernández, Vincendeau, Estelle, Serrat, Judit, Thouin, Alexander Marc, Susvirkar, Vivek, Lescale, Chloé, Paniagua, Inés, Hoekman, Liesbeth, Kaur, Simranjeet, Altelaar, Maarten, Deriano, Ludovic, Faesen, Alex C, Jacobs, Jacqueline J L, Afd Biomol.Mass Spect. and Proteomics, Biomolecular Mass Spectrometry and Proteomics
Publikováno v:
Nature Communications
Nature Communications, Nature Publishing Group, 2021, 12 (1), pp.5421. ⟨10.1038/s41467-021-25724-y⟩
Nature Communications, Vol 12, Iss 1, Pp 1-15 (2021)
Nature Communications, 12(1). Nature Publishing Group
Nature Communications, 2021, 12 (1), pp.5421. ⟨10.1038/s41467-021-25724-y⟩
Nature Communications, Nature Publishing Group, 2021, 12 (1), ⟨10.1038/s41467-021-25724-y⟩
Nature Communications, Nature Publishing Group, 2021, 12 (1), pp.5421. ⟨10.1038/s41467-021-25724-y⟩
Nature Communications, Vol 12, Iss 1, Pp 1-15 (2021)
Nature Communications, 12(1). Nature Publishing Group
Nature Communications, 2021, 12 (1), pp.5421. ⟨10.1038/s41467-021-25724-y⟩
Nature Communications, Nature Publishing Group, 2021, 12 (1), ⟨10.1038/s41467-021-25724-y⟩
MAD2L2 (REV7) plays an important role in DNA double-strand break repair. As a member of the shieldin complex, consisting of MAD2L2, SHLD1, SHLD2 and SHLD3, it controls DNA repair pathway choice by counteracting DNA end-resection. Here we investigated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e0eef28d1f10f82de63f851b152c960
https://hdl.handle.net/21.11116/0000-000A-7D73-921.11116/0000-000A-7D6F-F
https://hdl.handle.net/21.11116/0000-000A-7D73-921.11116/0000-000A-7D6F-F
Autor:
Loelia Babin, Caroline Demangel, Hélène Lenden-Hasse, Ludovic Deriano, Ludivine Baron, Erika Brunet, José Yélamos, Marie Bedora-Faure, Wei Yu, Chloé Lescale
Publikováno v:
Nature Communications
Nature Communications, Nature Publishing Group, 2020, 11 (1), pp.5239. ⟨10.1038/s41467-020-19060-w⟩
Nature Communications, 2020, 11 (1), pp.5239. ⟨10.1038/s41467-020-19060-w⟩
Nature Communications, Vol 11, Iss 1, Pp 1-15 (2020)
Nature Communications, Nature Publishing Group, 2020, 11 (1), pp.5239. ⟨10.1038/s41467-020-19060-w⟩
Nature Communications, 2020, 11 (1), pp.5239. ⟨10.1038/s41467-020-19060-w⟩
Nature Communications, Vol 11, Iss 1, Pp 1-15 (2020)
The alternative non-homologous end-joining (NHEJ) pathway promotes DNA double-strand break (DSB) repair in cells deficient for NHEJ or homologous recombination, suggesting that it operates at all stages of the cell cycle. Here, we use an approach in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3732515aa216a36cf4ec687e59a5511b
https://hal-pasteur.archives-ouvertes.fr/pasteur-03262335/document
https://hal-pasteur.archives-ouvertes.fr/pasteur-03262335/document
Autor:
Wilhelm Vaysse-Zinkhöfer, David Viterbo, Stéphane Descorps-Declère, Lucie Poggi, Guy-Franck Richard, Valentine Mosbach
Publikováno v:
PLoS Genetics, Vol 16, Iss 7, p e1008924 (2020)
PLoS Genetics
PLoS Genetics, 2020, 16 (7), pp.e1008924. ⟨10.1371/journal.pgen.1008924⟩
PLoS Genetics
PLoS Genetics, 2020, 16 (7), pp.e1008924. ⟨10.1371/journal.pgen.1008924⟩
Microsatellites are short tandem repeats, ubiquitous in all eukaryotes and represent ~2% of the human genome. Among them, trinucleotide repeats are responsible for more than two dozen neurological and developmental disorders. Targeting microsatellite
Autor:
Pierre Khalfi, Valérie Thiers, Jean-Pierre Vartanian, Noémie Berry, Wenjuan Jiao, Vincent Caval, Rodolphe Suspène, Emmanuelle Pitré, Simon Wain-Hobson
Publikováno v:
BMC Genomics
BMC Genomics, BioMed Central, 2019, 20 (1), pp.858. ⟨10.1186/s12864-019-6216-x⟩
BMC Genomics, 2019, 20 (1), pp.858. ⟨10.1186/s12864-019-6216-x⟩
BMC Genomics, Vol 20, Iss 1, Pp 1-12 (2019)
BMC Genomics, BioMed Central, 2019, 20 (1), pp.858. ⟨10.1186/s12864-019-6216-x⟩
BMC Genomics, 2019, 20 (1), pp.858. ⟨10.1186/s12864-019-6216-x⟩
BMC Genomics, Vol 20, Iss 1, Pp 1-12 (2019)
BackgroundAPOBEC1 (A1) enzymes are cytidine deaminases involved in RNA editing. In addition to this activity, a few A1 enzymes have been shown to be active on single stranded DNA. As two human ssDNA cytidine deaminases APOBEC3A (A3A), APOBEC3B (A3B)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f7d56105aea4dcdf3ee2f4f07cdc7ee
https://hal-pasteur.archives-ouvertes.fr/pasteur-02545764
https://hal-pasteur.archives-ouvertes.fr/pasteur-02545764
Publikováno v:
mBio
mBio, American Society for Microbiology, 2019, 10 (4), pp.e01252-19. ⟨10.1128/mBio.01252-19⟩
mBio, Vol 10, Iss 4, p e01252-19 (2019)
mBio, Vol 10, Iss 4 (2019)
mBio, American Society for Microbiology, 2019, 10 (4), pp.e01252-19. ⟨10.1128/mBio.01252-19⟩
mBio, Vol 10, Iss 4, p e01252-19 (2019)
mBio, Vol 10, Iss 4 (2019)
Chromosome damage must be repaired to prevent the proliferation of defective cells. Alternatively, cells with damage must be eliminated. This is true of human and several other cell types but may not be the case for single-celled parasites, such as t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::caa46167e05a82d5322cc74853814b72
https://hal-pasteur.archives-ouvertes.fr/pasteur-03107118/file/mBio-2019-Glover-e01252-19.full.pdf
https://hal-pasteur.archives-ouvertes.fr/pasteur-03107118/file/mBio-2019-Glover-e01252-19.full.pdf
Autor:
Wolf Dietrich Heyer, Aurèle Piazza
Publikováno v:
Trends in cell biology, vol 29, iss 2
Trends in Cell Biology
Trends in Cell Biology, 2019, 29 (2), pp.135-149. ⟨10.1016/j.tcb.2018.10.006⟩
Trends in Cell Biology, Elsevier, 2019, 29 (2), pp.135-149. ⟨10.1016/j.tcb.2018.10.006⟩
Trends in Cell Biology
Trends in Cell Biology, 2019, 29 (2), pp.135-149. ⟨10.1016/j.tcb.2018.10.006⟩
Trends in Cell Biology, Elsevier, 2019, 29 (2), pp.135-149. ⟨10.1016/j.tcb.2018.10.006⟩
International audience; The maintenance of genome integrity involves multiple independent DNA damage avoidance and repair mechanisms. However, the origin and pathways of the focal chromosomal reshuffling phenomena collectively referred to as chromoth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c2dd4d52521f2380667ed75af907f41
https://escholarship.org/uc/item/61c9v3w5
https://escholarship.org/uc/item/61c9v3w5
Publikováno v:
Current Genetics
Current Genetics, 2019, 65, pp.17-28. ⟨10.1007/s00294-018-0865-1⟩
Current Genetics, Springer Verlag, 2019, 65, pp.17-28. ⟨10.1007/s00294-018-0865-1⟩
Current Genetics, 2019, 65, pp.17-28. ⟨10.1007/s00294-018-0865-1⟩
Current Genetics, Springer Verlag, 2019, 65, pp.17-28. ⟨10.1007/s00294-018-0865-1⟩
International audience; Trinucleotide repeats are a particular class of microsatellites whose large expansions are responsible for at least two dozen human neurological and developmental disorders. Slippage of the two complementary DNA strands during
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a044ea1af10f5dd5095ad5e06bfa6f5
https://hal-pasteur.archives-ouvertes.fr/pasteur-02864590
https://hal-pasteur.archives-ouvertes.fr/pasteur-02864590