Literature DB >> 31600784

Loss of the nucleoporin Aladin in central nervous system and fibroblasts of Allgrove Syndrome.

Giacomo Bitetto1,2, Dario Ronchi1,2, Sara Bonato1,2, Alessandra Pittaro3,4, Giacomo Monzio Compagnoni1,2, Andreina Bordoni1,2, Sabrina Salani1,2, Emanuele Frattini1,2, Gianluca Lopez3,4, Fulvia Milena Cribiù3,4, Stefania Corti1,2, Giacomo P Comi1,2, Nereo Bresolin1,2, Alessio Di Fonzo1,2.   

Abstract

Allgrove syndrome (AS) is a rare disease with broad neurological involvement. Neurodegeneration can affect spinal motor neurons, Purkinje cells, striatal neurons and the autonomic system. The mechanisms that lead to neuronal loss are still unclear. Recessive mutations in the AAAS gene affect the encoded protein Aladin, which would normally localize to the cytoplasmic face of the nuclear membrane as part of the nuclear pore complex (NPC). While the NPC is known to be a key factor for nucleocytoplasmic transport, the precise role of Aladin has not been elucidated yet. Here, we explored the consequences of the homozygous AAAS mutation c.464G>A (p.R155H) in central nervous system tissues and fibroblasts of a novel AS patient presenting motor neuron disease, cerebellar ataxia and autonomic dysfunction. Neuropathological analyses showed severe loss of motor neurons and Purkinje cells, with significant reduction in the perinuclear expression of Aladin. A reduced amount of protein was detected in the nuclear membrane fraction of the patient's brain. RNA analysis revealed a significant reduction of the transcript AAAS-1, while the AAAS-2 transcript was upregulated in fibroblasts. To our knowledge, this is the first study to demonstrate the effects of AAAS mutations in the human central nervous system.
© The Author(s) 2019. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com.

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Year:  2019        PMID: 31600784     DOI: 10.1093/hmg/ddz236

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  4 in total

Review 1.  Nucleo-cytoplasmic transport defects and protein aggregates in neurodegeneration.

Authors:  Giacomo Bitetto; Alessio Di Fonzo
Journal:  Transl Neurodegener       Date:  2020-07-03       Impact factor: 8.014

2.  Protein signature of human skin fibroblasts allows the study of the molecular etiology of rare neurological diseases.

Authors:  Andreas Hentschel; Artur Czech; Ute Münchberg; Erik Freier; Ulrike Schara-Schmidt; Albert Sickmann; Jens Reimann; Andreas Roos
Journal:  Orphanet J Rare Dis       Date:  2021-02-09       Impact factor: 4.123

3.  A rare case of Allgrove Syndrome associated with growth hormone deficiency in an 8-year-Old child: A case report.

Authors:  Mahfoud Eid; Ahmad Chreitah; Omar Aljanati; Aria Mohammed; Ibrahim Melhem; Zeina Alkilany
Journal:  Ann Med Surg (Lond)       Date:  2022-08-18

Review 4.  Hypolacrimia and Alacrimia as Diagnostic Features for Genetic or Congenital Conditions.

Authors:  Marjolaine Willems; Constance F Wells; Christine Coubes; Marie Pequignot; Alison Kuony; Frederic Michon
Journal:  Invest Ophthalmol Vis Sci       Date:  2022-08-02       Impact factor: 4.925

  4 in total

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