Regulatory sites for splicing in human basal ganglia are enriched for disease-relevant information

Genome-wide association studies have generated an increasing number of common genetic variants associated with neurological and psychiatric disease risk. An improved understanding of the genetic control of gene expression in human brain is vital considering this is the likely modus operandum for man...

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Autores: Guelfi, Sebastian; D'Sa, Karishma; Botía, Juan A.|||0000-0002-6992-598X; Vandrovcova, Jana; Reynolds, Regina H.|||0000-0001-6470-7919; Zhang, David; Trabzuni, Daniah|||0000-0003-4826-9570; Collado-Torres, Leonardo|||0000-0003-2140-308X; Thomason, Andrew|||0000-0001-8240-1614; Quijada Leyton, Pedro; Gagliano Taliun, Sarah A.|||0000-0003-1306-1868; Nalls, Mike A.; Noyce, Alastair J.; Nicolas, Aaude; Cookson, Mark R.; Bandres-Ciga, Sara|||0000-0003-0056-1361; Gibbs, J. Raphael|||0000-0002-6985-0658; Hernandez, Dena G.|||0000-0002-0188-9927; Singleton, Andrew B.|||0000-0001-5606-700X; Reed, Xylena; Leonard, Hampton L.|||0000-0003-2390-8110; Blauwendraat, Cornelis|||0000-0001-9358-8111; Faghri, Faraz; Bras, Jose|||0000-0001-8186-0333; Guerreiro, Rita|||0000-0001-5879-3486; Tucci, Arianna|||0000-0001-5644-0070; Kia, Demis A.; Houlden, Henry|||0000-0002-2866-7777; Plun-Favreau, Helene; Mok, Kin Ying|||0000-0003-3145-880X; Wood, Nicholas W.|||0000-0002-9500-3348; Lovering, Ruth Caroline|||0000-0002-9791-0064; R'Bibo, Lea; Rizig, Mie|||0000-0003-2420-4449; Chelban, Viorica|||0000-0002-5817-6290; Tan, Manuela|||0000-0001-5835-669X; Morris, Huw|||0000-0002-5473-3774; Middlehurst, Ben; Quinn, John; Billingsley, Kimberley; Holmans, Peter|||0000-0003-0870-9412; Kinghorn, Kerri J.|||0000-0003-2048-4332; Lewis, Patrick|||0000-0003-4537-0489; Escott-Price, Valentina|||0000-0003-1784-5483; Williams, Nigel; Foltynie, Thomas|||0000-0003-0752-1813; Brice, Alexis|||0000-0002-0941-3990; Danjou, Fabrice|||0000-0002-4976-2327; Lesage, Suzanne; Corvol, Jean-Christophe|||0000-0001-7325-0199; Martinez, Maria M.; Giri, Anamika; Schulte, Claudia|||0000-0003-4006-1265; Brockmann, Kathrin|||0000-0002-7515-8596; Simón-Sánchez, Javier; Heutink, Peter|||0000-0001-5218-1737; Gasser, Thomas|||0000-0003-4882-2647; Rizzu, Patrizia; Sharma, Manu; Shulman, Joshua M.; Robak, Laurie; Lubbe, Steven; Mencacci, Niccolò Emanuele|||0000-0003-3383-9665; Finkbeiner, Steven; Lungu, Codrin; Scholz, Sonja|||0000-0002-6623-0429; Gan-Or, Ziv|||0000-0003-0332-234X; Rouleau, Guy A.|||0000-0001-8403-1418; Krohan, Lynne; van Hilten, Jacobus J.; Marinus, Johan; Adarmes-Gómez, A.D.|||0000-0002-1337-9289; Bernal-Bernal, Inmaculada; Bonilla-Toribio, Marta; Buiza-Rueda, Dolores|||0000-0002-3504-9299; Carrillo, Fátima; Carrión-Claro, M.; Mir, Pablo|||0000-0003-1656-302X; Gómez-Garre, Pilar|||0000-0002-0437-6182; Jesús, Silvia; Labrador-Espinosa, Miguel A.|||0000-0003-3576-1777; Macias, Daniel; Vargas-González, Laura; Méndez-del-Barrio, Carlota; Periñán, Teresa|||0000-0001-7412-7440; Tejera-Parrado, Cristina|||0000-0001-8001-5621; Diez-Fairen, Monica|||0000-0003-1882-0309; Aguilar, Miquel; Alvarez, Ignacio|||0000-0002-8537-3935; Boungiorno, María Teresa; Carcel, Maria; Pastor, Pau|||0000-0002-7493-8777; Tartari, Juan Pablo; Alvarez, Victoria|||0000-0002-1916-2523; Mendez-Gonzalez, Manuel|||0000-0002-5218-0774; Blázquez Estrada, Marta|||0000-0003-3348-9992; Garcia, Ciara; Suarez-Sanmartin, Esther; Barrero, Francisco Javier; Mondragon Rezola, Elisabet; Bergareche Yarza, Jesús Alberto; Gorostidi Pagola, Ana; de Munain Arregui, Adolfo López; Ruiz-Martínez, Javier; Cerdan, Debora|||0000-0001-5408-691X; Duarte, Jacinto; Clarimón, Jordi|||0000-0002-6824-6942; Dols Icardo, Oriol|||0000-0003-2656-8748; Infante, Jon|||0000-0003-4025-4606; Marín, Juan; Kulisevsky, Jaime|||0000-0003-4870-1431; Pagonabarraga Mora, Javier|||0000-0002-3248-704X; Gonzalez-Aramburu, Isabel|||0000-0002-3696-4093; Sanchez Rodriguez, Antonio; Sierra, Maria; Duran, Raquel; Ruz, Clara; Vives, Francisco; Escamilla Sevilla, Francisco|||0000-0003-2149-2668; Mínguez-Castellanos, Adolfo|||0000-0001-7086-1867; Cámara, Ana|||0000-0002-8005-9461; Compta, Yaroslau|||0000-0001-6443-0104; Ezquerra, Mario|||0000-0003-3246-6641; Marti, Maria Jose; Fernández, Manel; Muñoz, Esteban; Fernández-Santiago, Rubén|||0000-0002-4582-0702; Tolosa, Eduard|||0000-0001-6608-3038; Valldeoriola, Francesc|||0000-0002-8680-4274; García-Ruiz, Pedro; Gómez-Heredia, Maria José; Perez Errazquin, Francisco; Hoenicka, Janet|||0000-0002-6790-6988; Jiménez-Escrig, Adriano|||0000-0002-4927-1886; Martínez-Castrillo, Juan Carlos|||0000-0001-7744-6850; Lopez-Sendon, Jose Luis; Martinez Torres, Irene; Tabernero, Cesar; Vela, Lydia|||0000-0001-6663-395X; Zimprich, Alexander|||0000-0002-1668-5177; Pihlstrom, Lasse; Koks, Sulev; Taba, Pille|||0000-0002-1315-1065; Majamaa, Kari|||0000-0002-9070-3791; Siitonen, Ari; Okubadejo, Njideka|||0000-0003-2975-8803; Ojo, Oluwadamilola|||0000-0001-6461-2653; Forabosco, Paola|||0000-0002-2006-2693; Walker, Robert; Small, Kerrin|||0000-0003-4566-0005; Smith, Colin; Ramasamy, Adaikalavan|||0000-0002-7598-2892; Hardy, John|||0000-0002-3122-0423; Weale, Michael|||0000-0003-4593-1186; Ryten, Mina
Tipo de documento: Artículo
Fecha de publicación:2020
País:España
Institución:Universitat Autònoma de Barcelona
Repositorio:Dipòsit Digital de Documents de la UAB
Lenguaje:Inglés
OAI Identifier:oai:ddd.uab.cat:283724
Acceso en línea:https://ddd.uab.cat/record/283724
https://dx.doi.org/urn:doi:10.1038/s41467-020-14483-x
Nivel de acceso:Acceso abierto
Palabra clave:Gene regulation
Genetics of the nervous system
RNA sequencing
RNA splicing
Descripción
Sumario:Genome-wide association studies have generated an increasing number of common genetic variants associated with neurological and psychiatric disease risk. An improved understanding of the genetic control of gene expression in human brain is vital considering this is the likely modus operandum for many causal variants. However, human brain sampling complexities limit the explanatory power of brain-related expression quantitative trait loci (eQTL) and allele-specific expression (ASE) signals. We address this, using paired genomic and transcriptomic data from putamen and substantia nigra from 117 human brains, interrogating regulation at different RNA processing stages and uncovering novel transcripts. We identify disease-relevant regulatory loci, find that splicing eQTLs are enriched for regulatory information of neuron-specific genes, that ASEs provide cell-specific regulatory information with evidence for cellular specificity, and that incomplete annotation of the brain transcriptome limits interpretation of risk loci for neuropsychiatric disease. This resource of regulatory data is accessible through our web server, http://braineacv2.inf.um.es/.