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Loss of the fragile X syndrome protein FMRP results in misregulation of nonsense-mediated mRNA decay

Loss of the fragile X protein FMRP is a leading cause of intellectual disability and autism(1,2), but the underlying mechanism remains poorly understood. We report that FMRP deficiency results in hyperactivated nonsense-mediated mRNA decay (NMD)(3,4) in human SH-SY5Y neuroblastoma cells and fragile...

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Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Nat Cell Biol
Egile Nagusiak: Kurosaki, Tatsuaki, Imamachi, Naoto, Pröschel, Christoph, Mitsutomi, Shuhei, Nagao, Rina, Akimitsu, Nobuyoshi, Maquat, Lynne E.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 2021
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC8273690/
https://ncbi.nlm.nih.gov/pubmed/33420492
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41556-020-00618-1
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