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One-carbon cycle alterations induced by Dyrk1a dosage
- Source :
- Molecular Genetics and Metabolism Reports, Vol 1, Iss C, Pp 487-492 (2014), Molecular Genetics and Metabolism Reports, Digital.CSIC. Repositorio Institucional del CSIC, instname
- Publication Year :
- 2014
- Publisher :
- Elsevier, 2014.
-
Abstract
- © 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.<br />This work was supported by the Fondation Jérôme Lejeune (30CA1140087) and the Association Gaspard Félix (L'AGAFE) (30S1B07)
- Subjects :
- medicine.medical_specialty
Hyperhomocysteinemia
GK, Goto-Kakizaki
Homocysteine
DYRK1A
DYRK, dual-specificity tyrosine-(Y)-phosphorylation regulated kinase
Short Communication
Transsulfuration
PLP, pyridoxal phosphate
Biology
NQO1, NAD(P)H:quinone oxidoreductase
hcy, homocysteine
chemistry.chemical_compound
Endocrinology
Internal medicine
Genetics
medicine
SAHH, SAH hydrolase
PTZ, pentylenetetrazole
Molecular Biology
lcsh:QH301-705.5
Cystathionine beta synthase
lcsh:R5-920
Methionine
GABA, gamma-amino-butyric-acid
SAH, S-adenosylhomocysteine
medicine.disease
DS, Down syndrome
CBS, cystathionine beta synthase
chemistry
Biochemistry
Liver
lcsh:Biology (General)
biology.protein
Dyrk1a
Murine model
EGCG, epigallocatechin-gallate
Signal transduction
lcsh:Medicine (General)
Cysteine
Subjects
Details
- Language :
- English
- ISSN :
- 22144269
- Volume :
- 1
- Database :
- OpenAIRE
- Journal :
- Molecular Genetics and Metabolism Reports
- Accession number :
- edsair.doi.dedup.....f108e23c05bbadaab2c2a13ce888f782