Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Isabelle Canal"'
Autor:
Lydia Hadjeras, Marie Bouvier, Isabelle Canal, Leonora Poljak, Quentin Morin-Ogier, Carine Froment, Odile Burlet-Schlitz, Lina Hamouche, Laurence Girbal, Muriel Cocaign-Bousquet, Agamemnon J Carpousis
Publikováno v:
PLoS Biology, Vol 21, Iss 1, p e3001942 (2023)
RNA processing and degradation shape the transcriptome by generating stable molecules that are necessary for translation (rRNA and tRNA) and by facilitating the turnover of mRNA, which is necessary for the posttranscriptional control of gene expressi
Externí odkaz:
https://doaj.org/article/3e65891bf00f4059945dafbd6e7a7916
Autor:
Lydia Hadjeras, Marie Bouvier, Isabelle Canal, Leonora Poljak, Quentin Morin-Ogier, Carine Froment, Odile Burlet-Schlitz, Lina Hamouche, Laurence Girbal, Muriel Cocaign-Bousquet, Agamemnon J. Carpousis
BackgroundRNase E has crucial roles in the initiation of mRNA degradation, the processing of ‘stable’ transcripts such as rRNA and tRNA, and the quality control of ribosomes. With over 20’000 potential cleavage sites, RNase E is a low specifici
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bea65f9cfb53b48abfb873333b1b7047
https://doi.org/10.1101/2022.06.14.496040
https://doi.org/10.1101/2022.06.14.496040
Autor:
Marie Bouvier, Lydia Hadjeras, Agamemnon J. Carpousis, Muriel Cocaign-Bousquet, Quentin Morin‐Ogier, Isabelle Canal, Leonora Poljak, Laurence Girbal
Publikováno v:
Molecular Microbiology
Molecular Microbiology, Wiley, 2019, 111 (6), pp.1715-1731. ⟨10.1111/mmi.14248⟩
Molecular Microbiology, 2019, 111 (6), pp.1715-1731. ⟨10.1111/mmi.14248⟩
Molecular Microbiology, Wiley, 2019, 111 (6), pp.1715-1731. ⟨10.1111/mmi.14248⟩
Molecular Microbiology, 2019, 111 (6), pp.1715-1731. ⟨10.1111/mmi.14248⟩
Summary The reason for RNase E attachment to the inner membrane is largely unknown. To understand the cell biology of RNA degradation, we have characterized a strain expressing RNase E lacking the membrane attachment site (cytoplasmic RNase E). Genom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b09df87dcb2307ce7d175a5a5c18996
https://hal.archives-ouvertes.fr/hal-02317164
https://hal.archives-ouvertes.fr/hal-02317164
Autor:
Isabelle Canal, Olivier Fayet, Pavel V. Baranov, M.-F. Prère, Andrew E. Firth, Virag Sharma, John F. Atkins
Publikováno v:
Nucleic Acids Research
Nucleic Acids Research, Oxford University Press, 2014, pp.7210-7225
Nucleic Acids Research, Oxford University Press, 2014, pp.7210-7225
Programmed ribosomal -1 frameshifting is a non-standard decoding process occurring when ribosomes encounter a signal embedded in the mRNA of certain eukaryotic and prokaryotic genes. This signal has a mandatory component, the frameshift motif: it is
Publikováno v:
Journal of Bacteriology
Journal of Bacteriology, American Society for Microbiology, 2011, 193, pp.2735-2744
Journal of Bacteriology, American Society for Microbiology, 2011, 193, pp.2735-2744
The IS 911 bacterial transposable element uses −1 programmed translational frameshifting to generate the protein required for its mobility: translation initiated in one gene ( orfA ) shifts to the −1 frame and continues in a second overlapping ge
Publikováno v:
Journal of Biological Chemistry. 283:20421-20432
Nearly all members of a widespread family of bacterial transposable elements related to insertion sequence 3 (IS3), therefore called the IS3 family, very likely use programmed -1 ribosomal frameshifting to produce their transposase, a protein require
Autor:
Marie-Hélène, Mazauric, Patricia, Licznar, Marie-Françoise, Prère, Isabelle, Canal, Olivier, Fayet
Publikováno v:
The Journal of biological chemistry. 283(29)
Nearly all members of a widespread family of bacterial transposable elements related to insertion sequence 3 (IS3), therefore called the IS3 family, very likely use programmed -1 ribosomal frameshifting to produce their transposase, a protein require
Publikováno v:
FEMS microbiology letters. 218(2)
The IS911 bacterial transposable element has been analyzed for its mechanism of transposition and for the way it controls the expression of its genes by programmed −1 translational frameshifting. In the present study the prevalence of IS911 has bee