Por favor, use este identificador para citar o enlazar a este item: http://hdl.handle.net/10261/124337
COMPARTIR / EXPORTAR:
logo share SHARE logo core CORE BASE
Visualizar otros formatos: MARC | Dublin Core | RDF | ORE | MODS | METS | DIDL | DATACITE

Invitar a revisión por pares abierta
Título

One-carbon cycle alterations induced by Dyrk1a dosage

AutorDelabar, Jean M.; Latour, Alizée; Noll, Christophe; Renon, Marjorie; Salameh, Sacha; Paul, Jean Louis; Arbones, Maria L. CSIC ORCID ; Movassat, Jamileh; Janel, Nathalie
Palabras claveCystathionine beta synthase
Dyrk1a
Homocysteine
Liver
Murine model
Fecha de publicación2014
EditorElsevier
CitaciónMolecular Genetics and Metabolism Reports 1: 487-492 (2014)
Resumen© 2014 The Authors. Published by Elsevier Inc. Hyperhomocysteinemia due to cystathionine beta synthase deficiency confers diverse clinical manifestations. It is characterized by elevated plasma homocysteine levels, a common amino acid metabolized by remethylation to methionine or transsulfuration to cysteine.We recently found a relationship between hepaticDyrk1A protein expression, a serine/threonine kinase involved in signal transduction in biological processes, hepatic S-adenosylhomocysteine activity, and plasma homocysteine levels.We aimed to study whether there is also a relationship between Dyrk1a and cystathionine beta synthase activity. We used different murine models carrying altered gene coy numbers for Dyrk1a, and found a decreased cystathionine beta synthase activity in the liver of mice under-expressing Dyrk1a, and an increased in liver of mice over-expressing Dyrk1a. For each model, a positive correlation was found between cystathionine beta synthase activity and Dyrk1a protein expression in the liver of mice, which was confirmed in a non-modified genetic context. The positive correlation found between liver Dyrk1a protein expression and CBS activity in modified and non-modified genetic context strengthens the role of this kinase in one carbon metabolism.
Versión del editorhttp://dx.doi.org/10.1016/j.ymgmr.2014.11.004
URIhttp://hdl.handle.net/10261/124337
DOI10.1016/j.ymgmr.2014.11.004
Identificadoresdoi: 10.1016/j.ymgmr.2014.11.004
issn: 2214-4269
Aparece en las colecciones: (IBMB) Artículos




Ficheros en este ítem:
Fichero Descripción Tamaño Formato
Delabar-MGMR-2014-v1-p487.pdf516,72 kBAdobe PDFVista previa
Visualizar/Abrir
Mostrar el registro completo

CORE Recommender

PubMed Central
Citations

4
checked on 22-abr-2024

SCOPUSTM   
Citations

6
checked on 19-abr-2024

Page view(s)

295
checked on 24-abr-2024

Download(s)

248
checked on 24-abr-2024

Google ScholarTM

Check

Altmetric

Altmetric


Artículos relacionados:


Este item está licenciado bajo una Licencia Creative Commons Creative Commons