Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Lise-Marie Donnio"'
Autor:
Shaqraa Musawi, Lise-Marie Donnio, Zehui Zhao, Charlène Magnani, Phoebe Rassinoux, Olivier Binda, Jianbo Huang, Arnaud Jacquier, Laurent Coudert, Patrick Lomonte, Cécile Martinat, Laurent Schaeffer, Denis Mottet, Jocelyn Côté, Pierre-Olivier Mari, Giuseppina Giglia-Mari
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-17 (2023)
Abstract Spinal muscular atrophy is an autosomal recessive neuromuscular disease caused by mutations in the multifunctional protein Survival of Motor Neuron, or SMN. Within the nucleus, SMN localizes to Cajal bodies, which are associated with nucleol
Externí odkaz:
https://doaj.org/article/50248904959c4a86860e553b2d011862
Autor:
Jérémy Sandoz, Max Cigrang, Amélie Zachayus, Philippe Catez, Lise-Marie Donnio, Clèmence Elly, Jadwiga Nieminuszczy, Pietro Berico, Cathy Braun, Sergey Alekseev, Jean-Marc Egly, Wojciech Niedzwiedz, Giuseppina Giglia-Mari, Emmanuel Compe, Frédéric Coin
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-13 (2023)
Here the authors show that the exonuclease EXD2 is involved in the recovery of class II gene transcription after UV irradiation. EXD2 travels from the mitochondria to the nucleus to interact with RNA Pol II and degrade new synthetized mRNA to allow t
Externí odkaz:
https://doaj.org/article/a0d3f932123e4cc6bc846c308c77597d
Autor:
Lise-Marie Donnio, Elena Cerutti, Charlene Magnani, Damien Neuillet, Pierre-Olivier Mari, Giuseppina Giglia-Mari
Publikováno v:
eLife, Vol 11 (2022)
Xeroderma Pigmentosum group A-binding protein 2 (XAB2) is a multifunctional protein playing a critical role in distinct cellular processes including transcription, splicing, DNA repair, and messenger RNA export. In this study, we demonstrate that XAB
Externí odkaz:
https://doaj.org/article/119f8a3d1749498ca299e91af75c2f6f
Autor:
Florent Taupelet, Lise-Marie Donnio, Charlène Magnani, Pierre-Olivier Mari, Giuseppina Giglia-Mari
Publikováno v:
PLoS ONE, Vol 17, Iss 7, p e0271246 (2022)
Nucleotide Excision Repair is one of the five DNA repair systems. More than 30 proteins are involved in this process, including the seven XP proteins. When mutated, the genes coding for these proteins are provoking the rare disease Xeroderma Pigmento
Externí odkaz:
https://doaj.org/article/7b1c296f76e041699aa6dec994cc7775
Autor:
Lise-Marie Donnio, Catherine Miquel, Wim Vermeulen, Giuseppina Giglia-Mari, Pierre-Olivier Mari
Publikováno v:
Cancer Cell International, Vol 19, Iss 1, Pp 1-11 (2019)
Abstract Background The basal transcription/repair factor TFIIH is a ten sub-unit complex essential for RNA polymerase II (RNAP2) transcription initiation and DNA repair. In both these processes TFIIH acts as a DNA helix opener, required for promoter
Externí odkaz:
https://doaj.org/article/8066ce574fbb417e826aa5a18af95111
Autor:
Shaqraa Musawi, Lise-Marie Donnio, Charlène Magnani, Olivier Binda, Jocelyn Côté, Patrick Lomonte, Pierre-Olivier Mari, Giuseppina Giglia-Mari
SMA is an autosomal recessive neuromuscular disease caused by mutations in the multifunctional protein SMN. Within the nucleus, SMN localizes to Cajal bodies (CBs), which have been shown to be associated with nucleoli, nuclear organelles dedicated to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83426abd5bd6a4bf0532de60921e064d
https://hal.science/hal-03843781
https://hal.science/hal-03843781
Autor:
Elena Cerutti, Lise-Marie Donnio, Charlene Magnani, Damien Neuillet, Pierre-Olivier Mari, Giuseppina Giglia-Mari
Publikováno v:
eLife
eLife, 2022, 11, ⟨10.7554/elife.77094⟩
eLife, 2022, 11, ⟨10.7554/elife.77094⟩
Xeroderma Pigmentosum group A (XPA)-binding protein 2 (XAB2) is a multi-functional protein that plays a critical role in distinct cellular processes including transcription, splicing, DNA repair and mRNA export. In this study, we detailed XAB2 involv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9424f2c46d71f323441bf91f92bcee8f
https://doi.org/10.7554/elife.77094
https://doi.org/10.7554/elife.77094
Autor:
Jérémy Sandoz, Max Cigrang, Philippe Catez, Lise-Marie Donnio, Clèmence Elly, Pietro Berico, Cathy Braun, Sergey Alekseev, Jean-Marc Egly, Guiseppina Mari-Giglia, Emmanuel Compe, Frédéric Coin
The transcriptional response to genotoxic stress involves gene expression arrest, followed by recovery of mRNA synthesis (RRS) after DNA repair. Using a small-scale RNA interference screen, we found that the lack of the EXD2 nuclease impaired RRS and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f6dd5ba4fe8e672a10c1ffee28fe475
https://doi.org/10.1101/2022.07.20.499545
https://doi.org/10.1101/2022.07.20.499545
Autor:
Ambra Giglia-Mari, Florent TAUPELET, Charlène Magnani, Pierre-Olivier MARI, Lise-Marie DONNIO
Publikováno v:
PLoS ONE
PLoS ONE, 2022, 17 (7), pp.e0271246. ⟨10.1371/journal.pone.0271246⟩
PLoS ONE, 2022, 17 (7), pp.e0271246. ⟨10.1371/journal.pone.0271246⟩
Nucleotide Excision Repair is one of the five DNA repair systems. More than 30 proteins are involved in this process, including the seven XP proteins. When mutated, the genes coding for these proteins are provoking the rare disease Xeroderma Pigmento
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ae9d2dcde9b9c8ba76c8763e1e58df6
https://doi.org/10.1371/journal.pone.0271246
https://doi.org/10.1371/journal.pone.0271246