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Your search keyword '"T cell–restricted intracellular antigen-1 gene (TIA1)"' showing total 2 results
Start Over Descriptor "T cell–restricted intracellular antigen-1 gene (TIA1)" Topic t-cell intracellular antigen-1
2 results on '"T cell–restricted intracellular antigen-1 gene (TIA1)"'

1. No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patients.

Author

Baradaran-Heravi Y, Dillen L, Nguyen HP, Van Mossevelde S, Baets J, De Jonghe P, Engelborghs S, De Deyn PP, Vandenbulcke M, Vandenberghe R, Van Damme P, Cras P, Salmon E, Synofzik M, Heutink P, Wilke C, Simon-Sanchez J, Rojas-Garcia R, Turon-Sans J, Lleó A, Illán-Gala I, Clarimón J, Borroni B, Padovani A, Pastor P, Diez-Fairen M, Aguilar M, Gelpi E, Sanchez-Valle R, Borrego-Ecija S, Matej R, Parobkova E, Nacmias B, Sorbi S, Bagnoli S, de Mendonça A, Ferreira C, Fraidakis MJ, Diehl-Schmid J, Alexopoulos P, Almeida MR, Santana I, Van Broeckhoven C, and van der Zee J

Subjects
Cohort Studies, Female, Gene Frequency, Humans, Male, Mutation, Missense, White People genetics, Amyotrophic Lateral Sclerosis genetics, Frontotemporal Dementia genetics, T-Cell Intracellular Antigen-1 genetics
Abstract

We evaluated the genetic contribution of the T cell-restricted intracellular antigen-1 gene (TIA1) in a European cohort of frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS) patients. Exonic resequencing of TIA1 in 1120 patients (693 FTD, 341 ALS, 86 FTD-ALS) and 1039 controls identified in total 5 rare heterozygous missense variants, affecting the TIA1 low-complexity domain (LCD). Only 1 missense variant, p.Met290Thr, identified in a familial FTD patient with disease onset at 64 years, was absent from controls yet received a combined annotation-dependent depletion score of 11.42. By contrast, 3 of the 4 variants also detected in unaffected controls, p.Val294Glu, p.Gln318Arg, and p.Ala381Thr, had combined annotation-dependent depletion scores greater than 20. Our findings in a large European patient-control series indicate that variants in TIA1 are not a common cause of ALS and FTD. The observation of recurring TIA1 missense variants in unaffected individuals lead us to conclude that the exact genetic contribution of TIA1 to ALS and FTD pathogenesis remains to be further elucidated., (Copyright © 2018 The Authors. Published by Elsevier Inc. All rights reserved.)

Published
2018
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2. No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patients

Author

Ellen Gelpi, Mathieu Vandenbulcke, Yalda Baradaran-Heravi, Alex Michotte, Alexandre de Mendonça, Elisa Bonomi, Peter Paul De Deyn, Peter Heutink, Bruno Bergmans, Matthew J. Fraidakis, Matthis Synofzik, Dirk Peeters, Eva Parobkova, Christine Van Broeckhoven, Patrick Santens, Peter De Jonghe, Radoslav Matej, Maria Rosário Almeida, Rik Vandenberghe, Hung Phuoc Nguyen, Pau Pastor, Alessandro Padovani, Gabriel Miltenberger-Miltenyi, Jan De Bleecker, Philip Van Damme, Sara Van Mossevelde, Isabel Santana, Ricard Rojas-García, Olivier Deryck, Julie van der Zee, Eric Salmon, Ana Verdelho, Christiana Willems, Nina De Klippel, Miquel Aguilar, Lubina Dillen, Alberto Lleó, Sergi Borrego-Écija, Sebastiaan Engelborghs, Sandro Sorbi, Jonathan Baets, Camilla Ferrari, Monica Diez-Fairen, Silvia Bagnoli, Barbara Borroni, Raquel Sánchez-Valle, Johan Goeman, Anne Sieben, Ignacio Illán-Gala, Patrick Cras, Panagiotis Alexopoulos, Janina Turon-Sans, Benedetta Nacmias, Adrian Ivanoiu, Irene Piaceri, Janine Diehl-Schmid, Jan Versijpt, Silvana Archettim, C. Ferreira, Frederico Simões do Couto, Jordi Clarimón, Dirk Nuytten, Javier Simón-Sánchez, Carlo Wilke, UCL - SSS/IONS/NEUR - Clinical Neuroscience, UCL - (SLuc) Service de neurologie, BELNEU Consortium1, EU EOD Consortium, Clinical sciences, Neurology, and Pathologic Biochemistry and Physiology

Subjects
0301 basic medicine, Oncology, Male, Aging, Geriatrics & Gerontology, Gene mutation, Frontotemporal dementia (FTD), AMYOTROPHIC-LATERAL-SCLEROSIS, Pathogenesis, Cohort Studies, 0302 clinical medicine, Gene Frequency, Medicine and Health Sciences, Missense mutation, Amyotrophic lateral sclerosis (ALS), Amyotrophic lateral sclerosis, genetics [Frontotemporal Dementia], Medicine(all), General Neuroscience, ddc, genetics [Amyotrophic Lateral Sclerosis], genetics [European Continental Ancestry Group], Frontotemporal Dementia, Cohort, T cellerestricted intracellular antigen-1 gene (TIA1), Female, Life Sciences & Biomedicine, Cohort study, Frontotemporal dementia, medicine.medical_specialty, European Continental Ancestry Group, genetics [White People], Mutation, Missense, White People, 03 medical and health sciences, Internal medicine, mental disorders, medicine, Humans, ddc:610, genetics [T-Cell Intracellular Antigen-1], Biology, Allele frequency, T cell–restricted intracellular antigen-1 gene (TIA1), Science & Technology, business.industry, TIA1 protein, human, Amyotrophic Lateral Sclerosis, Neurosciences, TAR DNA-Binding protein 43 (TDP-43), FRONTOTEMPORAL DEMENTIA, medicine.disease, T-Cell Intracellular Antigen-1, 030104 developmental biology, Human medicine, Neurology (clinical), Neurosciences & Neurology, Geriatrics and Gerontology, business, 030217 neurology & neurosurgery, Developmental Biology
Abstract

We evaluated the genetic contribution of the T cell-restricted intracellular antigen-1 gene (TIA1) in a European cohort of frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS) patients. Exonic resequencing of TIA1 in 1120 patients (693 FTD, 341 ALS, 86 FTD-ALS) and 1039 controls identified in total 5 rare heterozygous missense variants, affecting the TIA1 low-complexity domain (LCD). Only 1 missense variant, p.Met290Thr, identified in a familial FTD patient with disease onset at 64 years, was absent from controls yet received a combined annotation-dependent depletion score of 11.42. By contrast, 3 of the 4 variants also detected in unaffected controls, p.Val294Glu, p.Gln318Arg, and p.Ala381Thr, had combined annotation-dependent depletion scores greater than 20. Our findings in a large European patient-control series indicate that variants in TIA1 are not a common cause of ALS and FTD. The observation of recurring TIA1 missense variants in unaffected individuals lead us to conclude that the exact genetic contribution of TIA1 to ALS and FTD pathogenesis remains to be further elucidated. ispartof: NEUROBIOLOGY OF AGING vol:69 ispartof: location:United States status: published

Published
2018
Full Text
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