Circadian Analysis of the Mouse Cerebellum Proteome.


Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
15 Apr 2019
Historique:
received: 29 03 2019
revised: 10 04 2019
accepted: 11 04 2019
entrez: 18 4 2019
pubmed: 18 4 2019
medline: 17 8 2019
Statut: epublish

Résumé

The cerebellum contains a circadian clock, generating internal temporal signals. The daily oscillations of cerebellar proteins were investigated in mice using a large-scale two-dimensional difference in gel electrophoresis (2D-DIGE). Analysis of 2D-DIGE gels highlighted the rhythmic variation in the intensity of 27/588 protein spots (5%) over 24 h based on cosinor regression. Notably, the rhythmic expression of most abundant cerebellar proteins was clustered in two main phases (i.e., midday and midnight), leading to bimodal distribution. Only six proteins identified here to be rhythmic in the cerebellum are also known to oscillate in the suprachiasmatic nuclei, including two proteins involved in the synapse activity (Synapsin 2 [SYN2] and vesicle-fusing ATPase [NSF]), two others participating in carbohydrate metabolism (triosephosphate isomerase (TPI1] and alpha-enolase [ENO1]), Glutamine synthetase (GLUL), as well as Tubulin alpha (TUBA4A). Most oscillating cerebellar proteins were not previously identified in circadian proteomic analyses of any tissue. Strikingly, the daily accumulation of mitochondrial proteins was clustered to the mid-resting phase, as previously observed for distinct mitochondrial proteins in the liver. Moreover, a number of rhythmic proteins, such as SYN2, NSF and TPI1, were associated with non-rhythmic mRNAs, indicating widespread post-transcriptional control in cerebellar oscillations. Thus, this study highlights extensive rhythmic aspects of the cerebellar proteome.

Identifiants

pubmed: 30991638
pii: ijms20081852
doi: 10.3390/ijms20081852
pmc: PMC6515515
pii:
doi:

Substances chimiques

Proteome 0
RNA, Messenger 0

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : French Proteomic Infrastructure
ID : ANR-10-INSB-08-03
Organisme : Idex Université de Strasbourg
ID : H2E

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Auteurs

Marine Plumel (M)

Institut Pluridisciplinaire Hubert Curien, LSMBO, Centre National de la Recherche Scientifique (CNRS), Université de Strasbourg, 67087 Strasbourg, France. marine.plumel@gmail.com.

Stéphanie Dumont (S)

Institute of Cellular and Integrative Neurosciences, CNRS, Université de Strasbourg, 67000 Strasbourg, France. dumonts@inci-cnrs.unistra.fr.

Pauline Maes (P)

Institut Pluridisciplinaire Hubert Curien, LSMBO, Centre National de la Recherche Scientifique (CNRS), Université de Strasbourg, 67087 Strasbourg, France. Pauline.Maes@u-bourgogne.fr.

Cristina Sandu (C)

Institute of Cellular and Integrative Neurosciences, CNRS, Université de Strasbourg, 67000 Strasbourg, France. sandu@inci-cnrs.unistra.fr.

Marie-Paule Felder-Schmittbuhl (MP)

Institute of Cellular and Integrative Neurosciences, CNRS, Université de Strasbourg, 67000 Strasbourg, France. feldermp@inci-cnrs.unistra.fr.

Etienne Challet (E)

Institute of Cellular and Integrative Neurosciences, CNRS, Université de Strasbourg, 67000 Strasbourg, France. challet@inci-cnrs.unistra.fr.

Fabrice Bertile (F)

Institut Pluridisciplinaire Hubert Curien, LSMBO, Centre National de la Recherche Scientifique (CNRS), Université de Strasbourg, 67087 Strasbourg, France. fbertile@unistra.fr.

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Classifications MeSH