Methylation-dependent transcriptional ...
Type de document :
Article dans une revue scientifique
DOI :
URL permanente :
Titre :
Methylation-dependent transcriptional regulation of crescentin gene (creS) by GcrA in Caulobacter crescentus.
Auteur(s) :
Mohapatra, Saswat Sourav [Auteur]
Unité de Glycobiologie Structurale et Fonctionnelle - UMR 8576 [UGSF]
Fioravanti, Antonella [Auteur]
Unité de Glycobiologie Structurale et Fonctionnelle - UMR 8576 [UGSF]
Vandame, Pauline [Auteur]
Unité de Glycobiologie Structurale et Fonctionnelle - UMR 8576 [UGSF]
Spriet, Corentin [Auteur]
Unité de Glycobiologie Structurale et Fonctionnelle - UMR 8576 [UGSF]
Pini, Francesco [Auteur]
Unité de Glycobiologie Structurale et Fonctionnelle - UMR 8576 [UGSF]
Bompard, Coralie [Auteur]
Unité de Glycobiologie Structurale et Fonctionnelle - UMR 8576 [UGSF]
Blossey, Ralf [Auteur]
Unité de Glycobiologie Structurale et Fonctionnelle - UMR 8576 [UGSF]
Valette, Odile [Auteur]
Laboratoire de chimie bactérienne [LCB]
Biondi, Emanuele G [Auteur]
Laboratoire de chimie bactérienne [LCB]
Unité de Glycobiologie Structurale et Fonctionnelle - UMR 8576 [UGSF]
Fioravanti, Antonella [Auteur]
Unité de Glycobiologie Structurale et Fonctionnelle - UMR 8576 [UGSF]
Vandame, Pauline [Auteur]
Unité de Glycobiologie Structurale et Fonctionnelle - UMR 8576 [UGSF]
Spriet, Corentin [Auteur]

Unité de Glycobiologie Structurale et Fonctionnelle - UMR 8576 [UGSF]
Pini, Francesco [Auteur]
Unité de Glycobiologie Structurale et Fonctionnelle - UMR 8576 [UGSF]
Bompard, Coralie [Auteur]

Unité de Glycobiologie Structurale et Fonctionnelle - UMR 8576 [UGSF]
Blossey, Ralf [Auteur]

Unité de Glycobiologie Structurale et Fonctionnelle - UMR 8576 [UGSF]
Valette, Odile [Auteur]
Laboratoire de chimie bactérienne [LCB]
Biondi, Emanuele G [Auteur]
Laboratoire de chimie bactérienne [LCB]
Titre de la revue :
Molecular Microbiology
Nom court de la revue :
Mol Microbiol
Numéro :
114
Pagination :
127-139
Date de publication :
2020-03-18
ISSN :
1365-2958
Mot(s)-clé(s) en anglais :
Caulobacter crescentus
CcrM
DNA methylation
GcrA
transcription
CcrM
DNA methylation
GcrA
transcription
Discipline(s) HAL :
Sciences du Vivant [q-bio]/Immunologie/Allergologie
Résumé en anglais : [en]
In Caulobacter crescentus the combined action of chromosome replication and the expression of DNA methyl-transferase CcrM at the end of S-phase maintains a cyclic alternation between a full- to hemi-methylated chromosome. ...
Lire la suite >In Caulobacter crescentus the combined action of chromosome replication and the expression of DNA methyl-transferase CcrM at the end of S-phase maintains a cyclic alternation between a full- to hemi-methylated chromosome. This transition of the chromosomal methylation pattern affects the DNA-binding properties of the transcription factor GcrA that controls the several key cell cycle functions. However, the molecular mechanism by which GcrA and methylation are linked to transcription is not fully elucidated yet. Using a combination of cell biology, genetics, and in vitro analysis, we deciphered how GcrA integrates the methylation pattern of several S-phase expressed genes to their transcriptional output. We demonstrated in vitro that transcription of ctrA from the P1 promoter in its hemi-methylated state is activated by GcrA, while in its fully methylated state GcrA had no effect. Further, GcrA and methylation together influence a peculiar distribution of creS transcripts, encoding for crescentin, the protein responsible for the characteristic shape of Caulobacter cells. This gene is duplicated at the onset of chromosome replication and the two hemi-methylated copies are spatially segregated. Our results indicated that GcrA transcribed only the copy where coding strand is methylated. In vitro transcription assay further substantiated this finding. As several of the cell cycle-regulated genes are also under the influence of methylation and GcrA-dependent transcriptional regulation, this could be a mechanism responsible for maintaining the gene transcription dosage during the S-phase.Lire moins >
Lire la suite >In Caulobacter crescentus the combined action of chromosome replication and the expression of DNA methyl-transferase CcrM at the end of S-phase maintains a cyclic alternation between a full- to hemi-methylated chromosome. This transition of the chromosomal methylation pattern affects the DNA-binding properties of the transcription factor GcrA that controls the several key cell cycle functions. However, the molecular mechanism by which GcrA and methylation are linked to transcription is not fully elucidated yet. Using a combination of cell biology, genetics, and in vitro analysis, we deciphered how GcrA integrates the methylation pattern of several S-phase expressed genes to their transcriptional output. We demonstrated in vitro that transcription of ctrA from the P1 promoter in its hemi-methylated state is activated by GcrA, while in its fully methylated state GcrA had no effect. Further, GcrA and methylation together influence a peculiar distribution of creS transcripts, encoding for crescentin, the protein responsible for the characteristic shape of Caulobacter cells. This gene is duplicated at the onset of chromosome replication and the two hemi-methylated copies are spatially segregated. Our results indicated that GcrA transcribed only the copy where coding strand is methylated. In vitro transcription assay further substantiated this finding. As several of the cell cycle-regulated genes are also under the influence of methylation and GcrA-dependent transcriptional regulation, this could be a mechanism responsible for maintaining the gene transcription dosage during the S-phase.Lire moins >
Langue :
Anglais
Comité de lecture :
Oui
Audience :
Non spécifiée
Établissement(s) :
Université de Lille
CNRS
CNRS
Équipe(s) de recherche :
Plant Storage Polysaccharides
Computational Molecular Systems Biology
Computational Molecular Systems Biology
Plateforme(s) de recherche :
Traitement de l'image et du signal pour la biologie (TISBio)
Date de dépôt :
2020-07-06T14:23:52Z
2020-09-28T10:23:38Z
2020-11-27T13:03:47Z
2021-12-09T11:42:17Z
2020-09-28T10:23:38Z
2020-11-27T13:03:47Z
2021-12-09T11:42:17Z
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