Inherited disorders of cobalamin metabolism disrupt nucleocytoplasmic transport of mRNA through impaired methylation/phosphorylation of ELAVL1/HuR

Author:

Battaglia-Hsu Shyue-Fang1,Ghemrawi Rose1,Coelho David1,Dreumont Natacha1,Mosca Pauline1,Hergalant Sébastien1,Gauchotte Guillaume1,Sequeira Jeffrey M2,Ndiongue Mariam1,Houlgatte Rémi1,Alberto Jean-Marc1,Umoret Remy1,Robert Aurélie1,Paoli Justine1,Jung Martin3,Quadros Edward V2,Guéant Jean-Louis1

Affiliation:

1. INSERM UMRS 954 NGERE – Nutrition, Genetics, and Environmental Risk Exposure and National Center of Inborn Errors of Metabolism, Faculty of Medicine of Nancy, University of Lorraine and University Regional Hospital Center of Nancy, Vandoeuvre-lès-Nancy, F-54000, France

2. Division of Hematology/Oncology, Department of Medicine, SUNY-Downstate Medical Center, Brooklyn, New York, NY, USA

3. Department of Medical Biochemistry and Molecular Biology, Saarland University, Building 44, Homburg 66421, Germany

Publisher

Oxford University Press (OUP)

Subject

Genetics

Reference43 articles.

1. Lessons in biology from patients with inborn errors of vitamin B12 metabolism;Watkins;Biochimie,2013

2. Molecular and cellular effects of vitamin B12 in brain, myocardium and liver through its role as co-factor of methionine synthase;Gueant;Biochimie,2013

3. Vitamin B12 deficiency in the brain leads to DNA hypomethylation in the TCblR/CD320 knockout mouse;Fernandez-Roig;Nutr. Metab. (Lond.),2012

4. Cellular uptake of cobalamin: transcobalamin and the TCblR/CD320 receptor;Quadros;Biochimie,2013

5. Decreased vitamin B12 availability induces ER stress through impaired SIRT1-deacetylation of HSF1;Ghemrawi;Cell Death Dis.,2013

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