Literature DB >> 31178128

Pathogenic Variants in NUP214 Cause "Plugged" Nuclear Pore Channels and Acute Febrile Encephalopathy.

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.
Copyright © 2019 American Society of Human Genetics. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  NUP214; NUP88; central channel particles; febrile encephalopathy; neurodegeneration; nuclear pore complex; nucleoporins

Mesh:

Substances:

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


  51 in total

1.  Removal of a single pore subcomplex results in vertebrate nuclei devoid of nuclear pores.

Authors:  Amnon Harel; Arturo V Orjalo; Thomas Vincent; Aurelie Lachish-Zalait; Sanjay Vasu; Sundeep Shah; Ella Zimmerman; Michael Elbaum; Douglass J Forbes
Journal:  Mol Cell       Date:  2003-04       Impact factor: 17.970

Review 2.  The nuclear pore complex: a jack of all trades?

Authors:  Birthe Fahrenkrog; Joachim Köser; Ueli Aebi
Journal:  Trends Biochem Sci       Date:  2004-04       Impact factor: 13.807

3.  Nuclear pore complex structure and dynamics revealed by cryoelectron tomography.

Authors:  Martin Beck; Friedrich Förster; Mary Ecke; Jürgen M Plitzko; Frauke Melchior; Günther Gerisch; Wolfgang Baumeister; Ohad Medalia
Journal:  Science       Date:  2004-10-28       Impact factor: 47.728

Review 4.  Modularity within the architecture of the nuclear pore complex.

Authors:  Thomas U Schwartz
Journal:  Curr Opin Struct Biol       Date:  2005-04       Impact factor: 6.809

5.  Role of aromatic localization in the gating process of a potassium channel.

Authors:  Carmen Domene; Satyavani Vemparala; Michael L Klein; Catherine Vénien-Bryan; Declan A Doyle
Journal:  Biophys J       Date:  2005-09-16       Impact factor: 4.033

6.  Nup214 is required for CRM1-dependent nuclear protein export in vivo.

Authors:  Saskia Hutten; Ralph H Kehlenbach
Journal:  Mol Cell Biol       Date:  2006-09       Impact factor: 4.272

7.  Mutated nup62 causes autosomal recessive infantile bilateral striatal necrosis.

Authors:  Lina Basel-Vanagaite; Liora Muncher; Rachel Straussberg; Metsada Pasmanik-Chor; Michal Yahav; Limor Rainshtein; Christopher A Walsh; Nurit Magal; Ellen Taub; Valerie Drasinover; Hanna Shalev; Revital Attia; Gideon Rechavi; Amos J Simon; Mordechai Shohat
Journal:  Ann Neurol       Date:  2006-08       Impact factor: 10.422

8.  Familial infantile bilateral striatal necrosis: clinical features and response to biotin treatment.

Authors:  R Straussberg; Z Shorer; R Weitz; L Basel; L Kornreich; C I Corie; L Harel; R Djaldetti; J Amir
Journal:  Neurology       Date:  2002-10-08       Impact factor: 9.910

9.  The nuclear pore complex protein ALADIN is mislocalized in triple A syndrome.

Authors:  Janet M Cronshaw; Michael J Matunis
Journal:  Proc Natl Acad Sci U S A       Date:  2003-05-02       Impact factor: 11.205

10.  Nup358/RanBP2 attaches to the nuclear pore complex via association with Nup88 and Nup214/CAN and plays a supporting role in CRM1-mediated nuclear protein export.

Authors:  Rafael Bernad; Hella van der Velde; Maarten Fornerod; Helen Pickersgill
Journal:  Mol Cell Biol       Date:  2004-03       Impact factor: 4.272

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  13 in total

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Authors:  Alison M Muir; Jennifer L Cohen; Sarah E Sheppard; Pavithran Guttipatti; Tsz Y Lo; Natalie Weed; Dan Doherty; Danielle DeMarzo; Christina R Fagerberg; Lars Kjærsgaard; Martin J Larsen; Patrick Rump; Katharina Löhner; Yoel Hirsch; David A Zeevi; Elaine H Zackai; Elizabeth Bhoj; Yuanquan Song; Heather C Mefford
Journal:  Am J Hum Genet       Date:  2020-04-09       Impact factor: 11.025

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Authors:  Alyssa N Coyne; Jeffrey D Rothstein
Journal:  Nat Rev Neurol       Date:  2022-04-29       Impact factor: 42.937

3.  Pathogenic variants in nucleoporin TPR (translocated promoter region, nuclear basket protein) cause severe intellectual disability in humans.

Authors:  Nicole J Van Bergen; Katrina M Bell; Kirsty Carey; Russell Gear; Sean Massey; Edward K Murrell; Lyndon Gallacher; Kate Pope; Paul J Lockhart; Andrew Kornberg; Lynn Pais; Marzena Walkiewicz; Cas Simons; Vihandha O Wickramasinghe; Susan M White; John Christodoulou
Journal:  Hum Mol Genet       Date:  2022-02-03       Impact factor: 5.121

Review 4.  Nuclear Pore Dysfunction in Neurodegeneration.

Authors:  Olivia Spead; Benjamin L Zaepfel; Jeffrey D Rothstein
Journal:  Neurotherapeutics       Date:  2022-09-07       Impact factor: 6.088

5.  Neurogenetic fetal akinesia and arthrogryposis: genetics, expanding genotype-phenotypes and functional genomics.

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6.  G4C2 Repeat RNA Initiates a POM121-Mediated Reduction in Specific Nucleoporins in C9orf72 ALS/FTD.

Authors:  Alyssa N Coyne; Benjamin L Zaepfel; Lindsey Hayes; Boris Fitchman; Yuval Salzberg; En-Ching Luo; Kelly Bowen; Hannah Trost; Stefan Aigner; Frank Rigo; Gene W Yeo; Amnon Harel; Clive N Svendsen; Dhruv Sareen; Jeffrey D Rothstein
Journal:  Neuron       Date:  2020-07-15       Impact factor: 17.173

7.  Multi-layered proteomic analyses decode compositional and functional effects of cancer mutations on kinase complexes.

Authors:  Martin Mehnert; Rodolfo Ciuffa; Fabian Frommelt; Federico Uliana; Audrey van Drogen; Kilian Ruminski; Matthias Gstaiger; Ruedi Aebersold
Journal:  Nat Commun       Date:  2020-07-16       Impact factor: 14.919

Review 8.  MRNA Transcription, Translation, and Defects in Developmental Cognitive and Behavioral Disorders.

Authors:  Moyra Smith
Journal:  Front Mol Biosci       Date:  2020-09-25

Review 9.  Clinical Manifestations and Pathogenesis of Acute Necrotizing Encephalopathy: The Interface Between Systemic Infection and Neurologic Injury.

Authors:  Priya Shukla; Abby Mandalla; Matthew J Elrick; Arun Venkatesan
Journal:  Front Neurol       Date:  2022-01-04       Impact factor: 4.003

10.  Expanding the phenotype of NUP85 mutations beyond nephrotic syndrome to primary autosomal recessive microcephaly and Seckel syndrome spectrum disorders.

Authors:  Ethiraj Ravindran; Ramona Jühlen; Carlos H Vieira-Vieira; Thuong Ha; Yuval Salzberg; Boris Fichtman; Lena Luise-Becker; Nuno Martins; Sylvie Picker-Minh; Paraskevi Bessa; Peer Arts; Matilda R Jackson; Ajay Taranath; Benjamin Kamien; Christopher Barnett; Na Li; Victor Tarabykin; Gisela Stoltenburg-Didinger; Amnon Harel; Matthias Selbach; Achim Dickmanns; Birthe Fahrenkrog; Hao Hu; Hamish Scott; Angela M Kaindl
Journal:  Hum Mol Genet       Date:  2021-11-01       Impact factor: 5.121

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