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Pumilio-1 mediated translational control of claudin-5 at the blood-brain barrier.
Hashimoto, Yosuke; Greene, Chris; Hanley, Nicole; Hudson, Natalie; Henshall, David; Sweeney, Kieron J; O'Brien, Donncha F; Campbell, Matthew.
Afiliación
  • Hashimoto Y; Smurfit Institute of Genetics, Trinity College Dublin, Dublin 2, Ireland. HASHIMOY@tcd.ie.
  • Greene C; Smurfit Institute of Genetics, Trinity College Dublin, Dublin 2, Ireland.
  • Hanley N; Smurfit Institute of Genetics, Trinity College Dublin, Dublin 2, Ireland.
  • Hudson N; Smurfit Institute of Genetics, Trinity College Dublin, Dublin 2, Ireland.
  • Henshall D; Science Foundation Ireland Research Centre for Chronic and Rare Neurological Diseases, FutureNeuro, Royal College of Surgeons in Ireland (RCSI), University of Medicine and Health Sciences, Dublin, Ireland.
  • Sweeney KJ; Department of Physiology and Medical Physics, RCSI University of Medicine and Health Sciences, Dublin, Ireland.
  • O'Brien DF; Department of Neurosurgery, Beaumont Hospital, Dublin, Ireland.
  • Campbell M; Department of Neurosurgery, Beaumont Hospital, Dublin, Ireland.
Fluids Barriers CNS ; 21(1): 52, 2024 Jun 19.
Article en En | MEDLINE | ID: mdl-38898501
ABSTRACT
Claudin-5 is one of the most essential tight junction proteins at the blood-brain barrier. A single nucleotide polymorphism rs10314 is located in the 3'-untranslated region of claudin-5 and has been shown to be a risk factor for schizophrenia. Here, we show that the pumilio RNA-binding protein, pumilio-1, is responsible for rs10314-mediated claudin-5 regulation. The RNA sequence surrounding rs10314 is highly homologous to the canonical pumilio-binding sequence and claudin-5 mRNA with rs10314 produces 25% less protein due to its inability to bind to pumilio-1. Pumilio-1 formed cytosolic granules under stress conditions and claudin-5 mRNA appeared to preferentially accumulate in these granules. Added to this, we observed granular pumilio-1 in endothelial cells in human brain tissues from patients with psychiatric disorders or epilepsy with increased/accumulated claudin-5 mRNA levels, suggesting translational claudin-5 suppression may occur in a brain-region specific manner. These findings identify a key regulator of claudin-5 translational processing and how its dysregulation may be associated with neurological and neuropsychiatric disorders.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Barrera Hematoencefálica / Proteínas de Unión al ARN / Claudina-5 Límite: Animals / Humans Idioma: En Revista: Fluids Barriers CNS Año: 2024 Tipo del documento: Article País de afiliación: Irlanda

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Barrera Hematoencefálica / Proteínas de Unión al ARN / Claudina-5 Límite: Animals / Humans Idioma: En Revista: Fluids Barriers CNS Año: 2024 Tipo del documento: Article País de afiliación: Irlanda