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Worldwide distribution of the DCDC2 READ1 regulatory element and its relationship with phoneme variation across languages.
DeMille, Mellissa M C; Tang, Kevin; Mehta, Chintan M; Geissler, Christopher; Malins, Jeffrey G; Powers, Natalie R; Bowen, Beatrice M; Adams, Andrew K; Truong, Dongnhu T; Frijters, Jan C; Gruen, Jeffrey R.
Afiliação
  • DeMille MMC; Department of Pediatrics, Yale University School of Medicine, New Haven, CT 06520.
  • Tang K; Department of Linguistics, Zhejiang University, Hangzhou, 310058 Zhejiang, China.
  • Mehta CM; Department of Pediatrics, Yale University School of Medicine, New Haven, CT 06520.
  • Geissler C; Department of Linguistics, Yale University, New Haven, CT 06520.
  • Malins JG; Department of Pediatrics, Yale University School of Medicine, New Haven, CT 06520.
  • Powers NR; Haskins Laboratories, New Haven, CT 06511.
  • Bowen BM; Department of Genetics, Yale University School of Medicine, New Haven, CT 06520.
  • Adams AK; Department of Genetics, Yale University School of Medicine, New Haven, CT 06520.
  • Truong DT; Department of Genetics, Yale University School of Medicine, New Haven, CT 06520.
  • Frijters JC; Department of Pediatrics, Yale University School of Medicine, New Haven, CT 06520.
  • Gruen JR; Child and Youth Studies, Brock University, St. Catherine's, ON L2S 3A1, Canada.
Proc Natl Acad Sci U S A ; 115(19): 4951-4956, 2018 05 08.
Article em En | MEDLINE | ID: mdl-29666269
DCDC2 is a gene strongly associated with components of the phonological processing system in animal models and in multiple independent studies of populations and languages. We propose that it may also influence population-level variation in language component usage. To test this hypothesis, we investigated the evolution and worldwide distribution of the READ1 regulatory element within DCDC2, and compared its distribution with variation in different language properties. The mutational history of READ1 was estimated by examining primate and archaic hominin sequences. This identified duplication and expansion events, which created a large number of polymorphic alleles based on internal repeat units (RU1 and RU2). Association of READ1 alleles was studied with respect to the numbers of consonants and vowels for languages in 43 human populations distributed across five continents. Using population-based approaches with multivariate ANCOVA and linear mixed effects analyses, we found that the RU1-1 allele group of READ1 is significantly associated with the number of consonants within languages independent of genetic relatedness, geographic proximity, and language family. We propose that allelic variation in READ1 helped create a subtle cognitive bias that was amplified by cultural transmission, and ultimately shaped consonant use by different populations over time.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Variação Genética / Elementos de Resposta / Alelos / Idioma / Proteínas Associadas aos Microtúbulos Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Variação Genética / Elementos de Resposta / Alelos / Idioma / Proteínas Associadas aos Microtúbulos Idioma: En Ano de publicação: 2018 Tipo de documento: Article