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1.
Cell ; 145(7): 1036-48, 2011 Jun 24.
Artigo em Inglês | MEDLINE | ID: mdl-21703448

RESUMO

Ion channel mutations are an important cause of rare Mendelian disorders affecting brain, heart, and other tissues. We performed parallel exome sequencing of 237 channel genes in a well-characterized human sample, comparing variant profiles of unaffected individuals to those with the most common neuronal excitability disorder, sporadic idiopathic epilepsy. Rare missense variation in known Mendelian disease genes is prevalent in both groups at similar complexity, revealing that even deleterious ion channel mutations confer uncertain risk to an individual depending on the other variants with which they are combined. Our findings indicate that variant discovery via large scale sequencing efforts is only a first step in illuminating the complex allelic architecture underlying personal disease risk. We propose that in silico modeling of channel variation in realistic cell and network models will be crucial to future strategies assessing mutation profile pathogenicity and drug response in individuals with a broad spectrum of excitability disorders.


Assuntos
Epilepsia/genética , Perfilação da Expressão Gênica , Canais Iônicos/genética , Polimorfismo de Nucleotídeo Único , Simulação por Computador , Epistasia Genética , Hipocampo/metabolismo , Humanos , Mutação de Sentido Incorreto , Neurônios/metabolismo , Medição de Risco
2.
Science ; 316(5822): 240-3, 2007 Apr 13.
Artigo em Inglês | MEDLINE | ID: mdl-17431170

RESUMO

To understand the demographic history of rhesus macaques (Macaca mulatta) and document the extent of linkage disequilibrium (LD) in the genome, we partially resequenced five Encyclopedia of DNA Elements regions in 9 Chinese and 38 captive-born Indian rhesus macaques. Population genetic analyses of the 1467 single-nucleotide polymorphisms discovered suggest that the two populations separated about 162,000 years ago, with the Chinese population tripling in size since then and the Indian population eventually shrinking by a factor of four. Using coalescent simulations, we confirmed that these inferred demographic events explain a much faster decay of LD in Chinese (r(2) approximately 0.15 at 10 kilobases) versus Indian (r(2) approximately 0.52 at 10 kilobases) macaque populations.


Assuntos
Desequilíbrio de Ligação , Macaca mulatta/genética , Animais , China , DNA Mitocondrial , Demografia , Genética Médica , Humanos , Índia , Polimorfismo de Nucleotídeo Único
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