Literature DB >> 26208798

Mutational spectrum of the SPAST and ATL1 genes in Korean patients with hereditary spastic paraplegia.

Hyunwoong Park1, Seong-Ho Kang2, Seungman Park3, So Yeon Kim4, Soo Hyun Seo5, Seung Jun Lee5, Jung Ae Lee5, Sung Im Cho5, Jung-Joon Sung6, Kwang-Woo Lee6, Ji Yeon Kim7, Sung Sup Park8, Moon-Woo Seong9.   

Abstract

Hereditary spastic paraplegia (HSP) is a genetically heterogeneous group of diseases characterized by insidiously progressive lower-extremity weakness and spasticity. Spastic paraplegia 4 (SPAST) is the most common type of uncomplicated autosomal dominant HSP (40% of such cases), and spastic paraplegia 3A (ATL1) is the second most common. Here, we conducted mutational analysis of the SPAST and/or ATL1 genes in 206 unrelated patients with HSP. DNA sequencing and multiplex ligation-dependent probe amplification was used to analyze SPAST or ATL1 pathogenic variants. To confirm splice-site pathogenic variants, mRNA transcripts were analyzed by reverse transcription-polymerase chain reactions and sequencing. Among the 52 patients with medical records and SPAST or ATL1 gene pathogenic variants or novel unclassified variants, 50 showed spasticity or weakness in their lower extremities. We identified 16 known and 18 novel SPAST pathogenic variants and 2 known and a novel splicing pathogenic variants in ATL1. We also identified 4 unclassified SPAST variants in 5 patients and an unclassified ATL1 variant in 1 patient. Further, a novel leaky-splicing variant (c.1537-11A>G) was found in SPAST, which caused skipping of exon 13 or exons 13-14. Among the 206 unrelated patients with HSP, SPAST or ATL1 pathogenic variants and potentially pathogenic variants were identified in 52 patients, a low pathogenic variant rate compared to previous results. Results from our study suggest that other genes may be involved in HSP in the Korean population.
Copyright © 2015 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  ATL1; Gene; Hereditary spastic paraplegia; Pathogenic variants; SPAST; Sequencing

Mesh:

Substances:

Year:  2015        PMID: 26208798     DOI: 10.1016/j.jns.2015.07.024

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   3.181


  5 in total

Review 1.  Genotype-phenotype associations in hereditary spastic paraplegia: a systematic review and meta-analysis on 13,570 patients.

Authors:  Maryam Erfanian Omidvar; Shahram Torkamandi; Somaye Rezaei; Behnam Alipoor; Mir Davood Omrani; Hossein Darvish; Hamid Ghaedi
Journal:  J Neurol       Date:  2019-11-19       Impact factor: 4.849

2.  Evidence of mosaicism in SPAST variant carriers in four French families.

Authors:  Chloé Angelini; Cyril Goizet; Samia Ait Said; William Camu; Christel Depienne; Bénédicte Heron; Bophara Kol; Marine Guillaud-Bataille; Perrine Pennamen; Caroline Rooryck; Clarisse Scherer-Gagou; Laurène Tissier; Giovanni Stevanin; Eric Leguern; Guillaume Banneau
Journal:  Eur J Hum Genet       Date:  2021-05-06       Impact factor: 5.351

3.  Clinical features and genotype-phenotype correlation analysis in patients with ATL1 mutations: A literature reanalysis.

Authors:  Guo-Hua Zhao; Xiao-Min Liu
Journal:  Transl Neurodegener       Date:  2017-04-04       Impact factor: 8.014

4.  An allosteric network in spastin couples multiple activities required for microtubule severing.

Authors:  Colby R Sandate; Agnieszka Szyk; Elena A Zehr; Gabriel C Lander; Antonina Roll-Mecak
Journal:  Nat Struct Mol Biol       Date:  2019-07-08       Impact factor: 15.369

5.  An integrated modelling methodology for estimating global incidence and prevalence of hereditary spastic paraplegia subtypes SPG4, SPG7, SPG11, and SPG15.

Authors:  Geert Vander Stichele; Alexandra Durr; Grace Yoon; Rebecca Schüle; Craig Blackstone; Giovanni Esposito; Connor Buffel; Inês Oliveira; Christian Freitag; Stephane van Rooijen; Stéphanie Hoffmann; Leen Thielemans; Belinda S Cowling
Journal:  BMC Neurol       Date:  2022-03-24       Impact factor: 2.474

  5 in total

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