Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Gaëlle Philippin"'
Publikováno v:
PLoS Genetics, Vol 18, Iss 6, p e1010238 (2022)
During replication, the presence of unrepaired lesions results in the formation of single stranded DNA (ssDNA) gaps that need to be repaired to preserve genome integrity and cell survival. All organisms have evolved two major lesion tolerance pathway
Externí odkaz:
https://doaj.org/article/52cca27b24524a93897444ac0f6e4178
Publikováno v:
Nucleic Acids Research
Nucleic Acids Research, Oxford University Press, 2017, ⟨10.1093/nar/gkx217⟩
Nucleic Acids Research, 2017, ⟨10.1093/nar/gkx217⟩
Nucleic Acids Research, Oxford University Press, 2017, ⟨10.1093/nar/gkx217⟩
Nucleic Acids Research, 2017, ⟨10.1093/nar/gkx217⟩
The RecBCD complex is a key factor in DNA metabolism. This protein complex harbors a processive nuclease and two helicases activities that give it the ability to process duplex DNA ends. These enzymatic activities make RecBCD a major player in double
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44ab9300c8b61382cc70766a845f22f7
https://hal-amu.archives-ouvertes.fr/hal-01521383/file/Laureti_NAR_2017.pdf
https://hal-amu.archives-ouvertes.fr/hal-01521383/file/Laureti_NAR_2017.pdf
Autor:
Hisaji Maki, Tsutomu Katayama, Mio Ikeda, Gaëlle Philippin, Asako Furukohri, Edward L. Loechler, Masahiro Akiyama, Robert P. P. Fuchs
Publikováno v:
Nucleic Acids Research
Escherichia coli DNA polymerase IV (Pol IV, also known as DinB) is a Y-family DNA polymerase capable of catalyzing translesion DNA synthesis (TLS) on certain DNA lesions, and accumulating data suggest that Pol IV may play an important role in copying
Publikováno v:
Nucleic Acids Research
Nucleic Acids Research, 2012, 40 (18), pp.9036-9043. ⟨10.1093/nar/gks675⟩
Nucleic Acids Research, Oxford University Press, 2012, 40 (18), pp.9036-9043. ⟨10.1093/nar/gks675⟩
Nucleic Acids Research, 2012, 40 (18), pp.9036-9043. ⟨10.1093/nar/gks675⟩
Nucleic Acids Research, Oxford University Press, 2012, 40 (18), pp.9036-9043. ⟨10.1093/nar/gks675⟩
International audience; Although most deoxyribonucleic acid (DNA) lesions are accurately repaired before replication, replication across unrepaired lesions is the main source of point mutations. The lesion tolerance processes, which allow damaged DNA
Publikováno v:
DNA Repair
DNA Repair, 2014, 22, pp.133-136. ⟨10.1016/j.dnarep.2014.08.001⟩
DNA Repair, Elsevier, 2014, 22, pp.133-136. ⟨10.1016/j.dnarep.2014.08.001⟩
DNA Repair, 2014, 22, pp.133-136. ⟨10.1016/j.dnarep.2014.08.001⟩
DNA Repair, Elsevier, 2014, 22, pp.133-136. ⟨10.1016/j.dnarep.2014.08.001⟩
Adducts formed at the nucleophilic N7 position of guanine are the most abundant lesions produced by alkylating agents such as ethylene oxide (EO) and propylene oxide (PO). In order to investigate the intrinsic mutagenic potential of N 7-alkylguanine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1da7102247f3da96f1be3afb9e7f4a66
https://cea.hal.science/cea-02074395
https://cea.hal.science/cea-02074395
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 2014, 111 (15), pp.5526--5531
Proceedings of the National Academy of Sciences of the United States of America, 2014, 111 (15), pp.5526--5531. ⟨10.1073/pnas.1321008111⟩
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 2014, 111 (15), pp.5526--5531
Proceedings of the National Academy of Sciences of the United States of America, 2014, 111 (15), pp.5526--5531. ⟨10.1073/pnas.1321008111⟩
International audience; The encounter of a replication fork with a blocking DNA lesion is a common event that cells need to address properly to preserve genome integrity. Cells possess two main strategies to tolerate unrepaired lesions: potentially m
Autor:
Mauro Modesti, Robert P. P. Fuchs, Gerard Mazón, Gaëlle Philippin, Jean Cadet, Didier Gasparutto
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America
Proceedings of the National Academy of Sciences of the United States of America, 2010, 107 (42), pp.18050-18055. ⟨10.1073/pnas.1008635107⟩
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 2010, 107 (42), pp.18050-18055. ⟨10.1073/pnas.1008635107⟩
Proceedings of the National Academy of Sciences of the United States of America, 2010, 107 (42), pp.18050-18055. ⟨10.1073/pnas.1008635107⟩
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 2010, 107 (42), pp.18050-18055. ⟨10.1073/pnas.1008635107⟩
O 6 -alkylG adducts are highly mutagenic due to their capacity to efficiently form O 6 -alkylG:T mispairs during replication, thus triggering G→A transitions. Mutagenesis is largely prevented by repair strategies such as reversal by alkyltransferas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d72715b0a054dcf4f4ff2f2a928d357f
https://cea.hal.science/cea-02074463
https://cea.hal.science/cea-02074463
Autor:
Carole Alies, Gaëlle Philippin, Stéphane Coulon, Sharada Ramasubramanyan, Alan R. Lehmann, Robert P. P. Fuchs
Many DNA lesions cause pausing of replication forks at lesion sites; thus, generating gaps in the daughter strands that are filled-in by post-replication repair (PRR) pathways. In Saccharomyces cerevisiae, PRR involves translesion synthesis (TLS) med
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::340712e7f9d779eb22c1d868f9c258e5
https://europepmc.org/articles/PMC2892369/
https://europepmc.org/articles/PMC2892369/
Publikováno v:
DNA repair. 8(6)
O6-methylguanine adducts are potent pre-mutagenic lesions owing to their high capacity to direct mis-insertion of thymine when bypassed by replicative DNA polymerases. The strong mutagenic potential of these adducts is prevented by alkyltransferases