Rev-erbalpha2 mRNA encodes a stable protein ...
Type de document :
Article dans une revue scientifique: Article original
DOI :
PMID :
Titre :
Rev-erbalpha2 mRNA encodes a stable protein with a potential role in circadian clock regulation.
Auteur(s) :
Rambaud, Juliette [Auteur]
Laboratoire de Biologie Moléculaire de la Cellule [LBMC]
Triqueneaux, Gérard [Auteur]
Laboratoire de Biologie Moléculaire de la Cellule [LBMC]
Centre de génétique et de physiologie moléculaire et cellulaire [CGPhiMC]
Masse, Ingrid [Auteur]
Centre de génétique et de physiologie moléculaire et cellulaire [CGPhiMC]
Staels, Bart [Auteur]
Récepteurs nucléaires, maladies cardiovasculaires et diabète - U 1011 [RNMCD]
Laudet, Vincent [Auteur]
Institut de Génomique Fonctionnelle de Lyon [IGFL]
Benoit, Gérard [Auteur]
Centre de génétique et de physiologie moléculaire et cellulaire [CGPhiMC]
Laboratoire de Biologie Moléculaire de la Cellule [LBMC]
Triqueneaux, Gérard [Auteur]
Laboratoire de Biologie Moléculaire de la Cellule [LBMC]
Centre de génétique et de physiologie moléculaire et cellulaire [CGPhiMC]
Masse, Ingrid [Auteur]
Centre de génétique et de physiologie moléculaire et cellulaire [CGPhiMC]
Staels, Bart [Auteur]
Récepteurs nucléaires, maladies cardiovasculaires et diabète - U 1011 [RNMCD]
Laudet, Vincent [Auteur]
Institut de Génomique Fonctionnelle de Lyon [IGFL]
Benoit, Gérard [Auteur]
Centre de génétique et de physiologie moléculaire et cellulaire [CGPhiMC]
Titre de la revue :
Mol Endocrinol
Pagination :
630-9
Date de publication :
2009-05
Mot(s)-clé(s) :
Male
Immunoprecipitation
COS Cells
Messenger
Receptors
Transcription
Immunoprecipitation
COS Cells
Messenger
Receptors
Transcription
Mot(s)-clé(s) en anglais :
Animals
Blotting
Western
Cercopithecus aethiops
Circadian Rhythm
Computational Biology
DNA-Binding Proteins
Electrophoretic Mobility Shift Assay
Gene Expression Regulation
Mice
Nuclear Receptor Subfamily 1
Group D
Member 1
Promoter Regions
Genetic
Protein Isoforms
Protein Multimerization
RNA
Cytoplasmic and Nuclear
Reverse Transcriptase Polymerase Chain Reaction
Blotting
Western
Cercopithecus aethiops
Circadian Rhythm
Computational Biology
DNA-Binding Proteins
Electrophoretic Mobility Shift Assay
Gene Expression Regulation
Mice
Nuclear Receptor Subfamily 1
Group D
Member 1
Promoter Regions
Genetic
Protein Isoforms
Protein Multimerization
RNA
Cytoplasmic and Nuclear
Reverse Transcriptase Polymerase Chain Reaction
Discipline(s) HAL :
Sciences du Vivant [q-bio]/Biochimie, Biologie Moléculaire/Biologie moléculaire
Résumé en anglais : [en]
Circadian rhythms are observed in nearly all aspects of physiology and behavior. In mammals, such biological rhythms are supported by a complex network of self-sustained transcriptional loops and posttranslational ...
Lire la suite >Circadian rhythms are observed in nearly all aspects of physiology and behavior. In mammals, such biological rhythms are supported by a complex network of self-sustained transcriptional loops and posttranslational modifications, which regulate timely controlled production and degradation of critical factors on a 24-h basis. Among these factors, the orphan nuclear receptor rev-erbalpha plays an essential role by linking together positive and negative regulatory loops. As an essential part of the circadian core clock mechanism, REV-ERBalpha expression shows a precisely scheduled oscillation reflecting the tight control of its production and degradation. In previous studies, we identified two alternative transcripts encoding two protein variants referred to as REV-ERBalpha1 and -alpha2. Interestingly, recent work identified structural elements present only in REV-ERBalpha1 that controls its turnover and thereby influences circadian oscillations. In the present work, we comparatively analyze the two variants and show that REV-ERBalpha2 exhibits a half-life incompatible with a circadian function, suggesting that this variant exerts different biological functions. However, our comparative study clearly indicates undistinguishable DNA-binding properties and transcriptional repression activity as well as a similar regulation mechanism. The only consistent difference appears to be the relative expression level of the two transcripts, rev-erbalpha1 being one to 100 times more expressed than alpha2 depending on tissue and circadian time. Taking this finding into consideration, we reassessed REV-ERBalpha2 turnover and were able to show that this variant exhibits a reduced half-life when coexpressed with REV-ERBalpha1. We propose that the relative expression levels of the two REV-ERBalpha variants fine-tune the circadian period length by regulating REV-ERBalpha half-life.Lire moins >
Lire la suite >Circadian rhythms are observed in nearly all aspects of physiology and behavior. In mammals, such biological rhythms are supported by a complex network of self-sustained transcriptional loops and posttranslational modifications, which regulate timely controlled production and degradation of critical factors on a 24-h basis. Among these factors, the orphan nuclear receptor rev-erbalpha plays an essential role by linking together positive and negative regulatory loops. As an essential part of the circadian core clock mechanism, REV-ERBalpha expression shows a precisely scheduled oscillation reflecting the tight control of its production and degradation. In previous studies, we identified two alternative transcripts encoding two protein variants referred to as REV-ERBalpha1 and -alpha2. Interestingly, recent work identified structural elements present only in REV-ERBalpha1 that controls its turnover and thereby influences circadian oscillations. In the present work, we comparatively analyze the two variants and show that REV-ERBalpha2 exhibits a half-life incompatible with a circadian function, suggesting that this variant exerts different biological functions. However, our comparative study clearly indicates undistinguishable DNA-binding properties and transcriptional repression activity as well as a similar regulation mechanism. The only consistent difference appears to be the relative expression level of the two transcripts, rev-erbalpha1 being one to 100 times more expressed than alpha2 depending on tissue and circadian time. Taking this finding into consideration, we reassessed REV-ERBalpha2 turnover and were able to show that this variant exhibits a reduced half-life when coexpressed with REV-ERBalpha1. We propose that the relative expression levels of the two REV-ERBalpha variants fine-tune the circadian period length by regulating REV-ERBalpha half-life.Lire moins >
Langue :
Anglais
Comité de lecture :
Oui
Audience :
Internationale
Vulgarisation :
Non
Source :