| Literature DB >> 31178128 |
Boris Fichtman1, Tamar Harel2, Nitzan Biran1, Fadia Zagairy1, Carolyn D Applegate3, Yuval Salzberg1, Tal Gilboa4, Somaya Salah2, Avraham Shaag5, Natalia Simanovsky6, Houriya Ayoubieh7, Nara Sobreira7, Giuseppe Punzi8, Ciro Leonardo Pierri8, Ada Hamosh7, Orly Elpeleg5, Amnon Harel9, Simon Edvardson10.
Abstract
We report biallelic missense and frameshift pathogenic variants in the gene encoding human nucleoporin NUP214 causing acute febrile encephalopathy. Clinical symptoms include neurodevelopmental regression, seizures, myoclonic jerks, progressive microcephaly, and cerebellar atrophy. NUP214 and NUP88 protein levels were reduced in primary skin fibroblasts derived from affected individuals, while the total number and density of nuclear pore complexes remained normal. Nuclear transport assays exhibited defects in the classical protein import and mRNA export pathways in affected cells. Direct surface imaging of fibroblast nuclei by scanning electron microscopy revealed a large increase in the presence of central particles (known as "plugs") in the nuclear pore channels of affected cells. This observation suggests that large transport cargoes may be delayed in passage through the nuclear pore channel, affecting its selective barrier function. Exposure of fibroblasts from affected individuals to heat shock resulted in a marked delay in their stress response, followed by a surge in apoptotic cell death. This suggests a mechanistic link between decreased cell survival in cell culture and severe fever-induced brain damage in affected individuals. Our study provides evidence by direct imaging at the single nuclear pore level of functional changes linked to a human disease.Entities:
Keywords: NUP214; NUP88; central channel particles; febrile encephalopathy; neurodegeneration; nuclear pore complex; nucleoporins
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Year: 2019 PMID: 31178128 PMCID: PMC6612515 DOI: 10.1016/j.ajhg.2019.05.003
Source DB: PubMed Journal: Am J Hum Genet ISSN: 0002-9297 Impact factor: 11.043