Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Philippe Catez"'
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:
Jérémy Sandoz, Zita Nagy, Philippe Catez, Gizem Caliskan, Sylvain Geny, Jean-Baptiste Renaud, Jean-Paul Concordet, Arnaud Poterszman, Laszlo Tora, Jean-Marc Egly, Nicolas Le May, Frédéric Coin
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-14 (2019)
Chromatin structure plays a significant role in the regulation of gene expression. Here the authors show that TFIIH interacts with the histone acetyl transferase KAT2A and recruits the ATAC/hSAGA complexes to chromatin; and that loss of xeroderma pig
Externí odkaz:
https://doaj.org/article/c3b2c0ec8f5b4543bcc98340f8ba7994
Publikováno v:
PLoS Genetics, Vol 10, Iss 10, p e1004732 (2014)
The expression of protein-coding genes requires the selective role of many transcription factors, whose coordinated actions remain poorly understood. To further grasp the molecular mechanisms that govern transcription, we focused our attention on the
Externí odkaz:
https://doaj.org/article/d0105cf9646142f095af1cd13188f5b2
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:
Jean-Baptiste Renaud, Jérémy Sandoz, Jean-Paul Concordet, Philippe Catez, Sylvain Geny, Laszlo Tora, Gizem Caliskan, Arnaud Poterszman, Nicolas Le May, Jean-Marc Egly, Zita Nagy, Frédéric Coin
Publikováno v:
Nature Communications
Nature Communications, Nature Publishing Group, 2019, 10 (1), ⟨10.1038/s41467-019-09270-2⟩
Nature Communications, Vol 10, Iss 1, Pp 1-14 (2019)
Nature Communications, 2019, 10 (1), ⟨10.1038/s41467-019-09270-2⟩
Nature Communications, Nature Publishing Group, 2019, 10 (1), pp.1288. ⟨10.1038/s41467-019-09270-2⟩
Nature Communications, Nature Publishing Group, 2019, 10 (1), ⟨10.1038/s41467-019-09270-2⟩
Nature Communications, Vol 10, Iss 1, Pp 1-14 (2019)
Nature Communications, 2019, 10 (1), ⟨10.1038/s41467-019-09270-2⟩
Nature Communications, Nature Publishing Group, 2019, 10 (1), pp.1288. ⟨10.1038/s41467-019-09270-2⟩
The TFIIH subunit XPB is involved in combined Xeroderma Pigmentosum and Cockayne syndrome (XP-B/CS). Our analyses reveal that XPB interacts functionally with KAT2A, a histone acetyltransferase (HAT) that belongs to the hSAGA and hATAC complexes. XPB
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2af59dd46589be04d58d71b39649911
https://hal.archives-ouvertes.fr/hal-03092036
https://hal.archives-ouvertes.fr/hal-03092036
Publikováno v:
Molecular Cell. 16:187-197
Mutations in the XPD subunit of the transcription/repair factor TFIIH cause the Xeroderma pigmentosum disorder. We show that in some XP-D deficient cells, transactivation by the vitamin D receptor (VDR) is selectively inhibited for a subset of respon
Publikováno v:
PLoS Genetics
PLoS Genetics, Vol 10, Iss 10, p e1004732 (2014)
PLoS Genetics, Vol 10, Iss 10, p e1004732 (2014)
The expression of protein-coding genes requires the selective role of many transcription factors, whose coordinated actions remain poorly understood. To further grasp the molecular mechanisms that govern transcription, we focused our attention on the
Both XPD alleles contribute to the phenotype of compound heterozygote xeroderma pigmentosum patients
Publikováno v:
The Journal of Experimental Medicine
Mutations in the XPD subunit of the DNA repair/transcription factor TFIIH result in the rare recessive genetic disorder xeroderma pigmentosum (XP). Many XP patients are compound heterozygotes with a “causative” XPD point mutation R683W and differ
Autor:
Philippe Catez, Dominique Aunis, Dominique Lecestre, Olivier Rohr, Christian Schwartz, Evelyne Schaeffer
Publikováno v:
Journal of Virology
Journal of Virology, American Society for Microbiology, 2000, 74 (1), pp.65-73. ⟨10.1128/JVI.74.1.65-73.2000⟩
Journal of Virology, American Society for Microbiology, 2000, 74 (1), pp.65-73. ⟨10.1128/JVI.74.1.65-73.2000⟩
Human immunodeficiency virus type 1 (HIV-1) infects the central nervous system (CNS) and plays a direct role in the pathogenesis of AIDS dementia. However, mechanisms underlying HIV-1 gene expression in the CNS are poorly understood. The importance o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c070ce9a35310c8c252ada0b2291383
http://jvi.asm.org/cgi/doi/10.1128/JVI.74.1.65-73.2000
http://jvi.asm.org/cgi/doi/10.1128/JVI.74.1.65-73.2000