دورية أكاديمية

Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia

التفاصيل البيبلوغرافية
العنوان: Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia
المؤلفون: L. W. Bonham, N. Z. R. Steele, C. M. Karch, I. Broce, E. G. Geier, N. L. Wen, P. Momeni, J. Hardy, Z. A. Miller, M. L. Gorno-Tempini, C. P Hess, P. Lewis, B. L. Miller, W. W. Seeley, C. Manzoni, R. S. Desikan, S. E. Baranzini, R. Ferrari, J. S. Yokoyama, D. G. Hernandez, M. A. Nalls, J. D. Rohrer, A. Ramasamy, J. B. J. Kwok, C. Dobson-stone, P. R. Schofield, G. M. Halliday, J. R. Hodges, O. Piguet, L. Bartley, E. Thompson, E. Haan, I. Hernández, A. Ruiz, M. Boada, B. Borroni, A. padovani, C. Cruchaga, N. J. Cairns, L. Benussi, G. Binetti, R. Ghidoni, G. Forloni, D. Albani, D. Galimberti, C. Fenoglio, M. Serpente, E. Scarpini, J. Clarimón, A. Lleó, R. Blesa, M. Landqvist Waldö, K. Nilsson, C. Nilsson, I. R. A. Mackenzie, G. -Y. R. Hsiung, D. M. A. Mann, J. Grafman, C. M. Morris, J. Attems, T. D. Griffiths, I. G. McKeith, A. J. Thomas, P. Pietrini, E. D. Huey, E. M. Wassermann, A. Baborie, E. Jaros, M. C. Tierney, P. Pastor, C. Razquin, S. Ortega-Cubero, E. Alonso, R. Perneczky, J. Diehl-Schmid, P. Alexopoulos, A. Kurz, I. Rainero, E. Rubino, L. Pinessi, E. Rogaeva, P. St George-Hyslop, G. Rossi, F. tagliavini, G. Giaccone, J. B. Rowe, J. C. M. Schlachetzki, J. Uphill, J. Collinge, S. Mead, A. Danek, V. M. Van Deerlin, M. Grossman, J. Q. Trojanowski, J. van der Zee, M. Cruts, C. Van Broeckhoven, S. F. Cappa, I. Leber, D. Hannequin, V. Golfier, M. Vercelletto, A. Brice, B. Nacmias, S. Sorbi, S. Bagnoli, I. piaceri, J. E. Nielsen, L. E. Hjermind, M. Riemenschneider, M. Mayhaus, B. Ibach, G. Gasparoni, S. Pichler, W. Gu, M. N. Rossor, N. C. Fox, J. D. Warren, M. G. Spillantini, H. R. Morris, P. Rizzu, P. Heutink, J. S. Snowden, S. Rollinson, A. Richardson, A. Gerhard, A. C. Bruni, R. Maletta, F. Frangipane, C. Cupidi, L. Bernardi, M. Anfossi, M. Gallo, M. E. Conidi, N. Smirne, R. Rademakers, M. Baker, D. W. Dickson, N. R. Graff-Radford, R. C. Petersen, D. Knopman, K. A. Josephs, B. F. Boeve, J. E. Parisi, A. M. Karydas, H. Rosen, J. C. van Swieten, E. G. P. Dopper, H. seelaar, Y. A. L. Pijnenburg, P. Scheltens, G. Logroscino, R. Capozzo, V. Novelli, A. A. puca, M. Franceschi, A. Postiglione, G. Milan, P. Sorrentino, M. Kristiansen, H. -H. Chiang, C. Graff, F. Pasquier, A. Rollin, V. Deramecourt, T. Lebouvier, D. Kapogiannis, L. Ferrucci, S. Pickering-Brown, A. B. Singleton
المساهمون: L.W. Bonham, N.Z.R. Steele, C.M. Karch, I. Broce, E.G. Geier, N.L. Wen, P. Momeni, J. Hardy, Z.A. Miller, M.L. Gorno-Tempini, C.P He, P. Lewi, B.L. Miller, W.W. Seeley, C. Manzoni, R.S. Desikan, S.E. Baranzini, R. Ferrari, J.S.Yokoyama, D. G. Hernandez, M. A. Nall, J. D. Rohrer, A. Ramasamy, J. B. J. Kwok, C. Dobson-stone, P. R. Schofield, G. M. Halliday, J. R. Hodge, O. Piguet, L. Bartley, E. Thompson, E. Haan, I. Hernández, A. Ruiz, M. Boada, B. Borroni, A. padovani, C. Cruchaga, N. J. Cairn, L. Benussi, G. Binetti, R. Ghidoni, G. Forloni, D. Albani, D. Galimberti, C. Fenoglio, M. Serpente, E. Scarpini, J. Clarimón, A. Lleó, R. Blesa, M. Landqvist Waldö, K. Nilsson, C. Nilsson, I. R. A. Mackenzie, G. -Y. R. Hsiung, D. M. A. Mann, J. Grafman, C. M. Morri, J. Attem, T. D. Griffith, I. G. McKeith, A. J. Thoma, P. Pietrini, E. D. Huey, E. M. Wassermann, A. Baborie, E. Jaro, M. C. Tierney, P. Pastor, C. Razquin, S. Ortega-Cubero, E. Alonso, R. Perneczky, J. Diehl-Schmid, P. Alexopoulo, A. Kurz, I. Rainero, E. Rubino, L. Pinessi, E. Rogaeva, P. St George-Hyslop, G. Rossi, F. tagliavini, G. Giaccone, J. B. Rowe, J. C. M. Schlachetzki, J. Uphill, J. Collinge, S. Mead, A. Danek, V. M. Van Deerlin, M. Grossman, J. Q. Trojanowski, J. van der Zee, M. Crut, C. Van Broeckhoven, S. F. Cappa, I. Leber, D. Hannequin
سنة النشر: 2019
المجموعة: Università degli studi di Torino: AperTo (Archivio Istituzionale ad Accesso Aperto)
الوصف: The semantic variant of primary progressive aphasia (svPPA) is a clinical syndrome characterized by neurodegeneration and progressive loss of semantic knowledge. Unlike many other forms of frontotemporal lobar degeneration (FTLD), svPPA has a highly consistent underlying pathology composed of TDP-43 (a regulator of RNA and DNA transcription metabolism). Previous genetic studies of svPPA are limited by small sample sizes and a paucity of common risk variants. Despite this, svPPA's relatively homogenous clinicopathologic phenotype makes it an ideal investigative model to examine genetic processes that may drive neurodegenerative disease. In this study, we used GWAS metadata, tissue samples from pathologically confirmed frontotemporal lobar degeneration, and in silico techniques to identify and characterize protein interaction networks associated with svPPA risk. We identified 64 svPPA risk genes that interact at the protein level. The protein pathways represented in this svPPA gene network are critical regulators of RNA metabolism and cell death, such as SMAD proteins and NOTCH1. Many of the genes in this network are involved in TDP-43 metabolism. Contrary to the conventional notion that svPPA is a clinical syndrome with few genetic risk factors, our analyses show that svPPA risk is complex and polygenic in nature. Risk for svPPA is likely driven by multiple common variants in genes interacting with TDP-43, along with cell death, x' working in combination to promote neurodegeneration.
نوع الوثيقة: article in journal/newspaper
اللغة: English
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/31350420; info:eu-repo/semantics/altIdentifier/wos/WOS:000477698600012; volume:9; issue:1; firstpage:10854; lastpage:10866; numberofpages:13; journal:SCIENTIFIC REPORTS; https://hdl.handle.net/2318/1894675Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85069717816
DOI: 10.1038/s41598-019-46415-1
الإتاحة: https://doi.org/10.1038/s41598-019-46415-1Test
https://hdl.handle.net/2318/1894675Test
حقوق: info:eu-repo/semantics/openAccess
رقم الانضمام: edsbas.DD211523
قاعدة البيانات: BASE