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Effect of the mutation of promoter region in Wilson disease ATP7B gene on the expression of reporter gene / 中华医学遗传学杂志
Chinese Journal of Medical Genetics ; (6): 566-568, 2005.
Artigo em Chinês | WPRIM | ID: wpr-279999
ABSTRACT
<p><b>OBJECTIVE</b>To find out the relationship between mutation of ATP7B gene promoter region and pathogenesis of Wilson disease(WD).</p><p><b>METHODS</b>Two of 48 WD patients presented C-->T base substitution mutations at the position -183. DNA sequences of the promoter region from normal and mutant samples were separated. The fragments containing the promoter region were cloned upstream of the luciferase. Luciferase activity was analyzed.</p><p><b>RESULTS</b>The luciferase activity of reporter gene containing normal sequence of ATP7B gene promoter region did not show significant difference as compared with that of reporter gene containing mutant promoter(n=3, P > 0.05).</p><p><b>CONCLUSION</b>No influence of C-->T base substitution mutations on the activity of promoter was observed in study. The results suggest that WD pathogenesis relates little to the mutations of the promoter region in Chinese.</p>
Assuntos
Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Análise Mutacional de DNA / Sequência de Bases / Regiões Promotoras Genéticas / Adenosina Trifosfatases / Proteínas de Transporte de Cátions / Linhagem Celular Tumoral / ATPases Transportadoras de Cobre / Genética / Degeneração Hepatolenticular / Luciferases Limite: Adolescente / Adulto / Criança / Feminino / Humanos / Masculino Idioma: Chinês Revista: Chinese Journal of Medical Genetics Ano de publicação: 2005 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Análise Mutacional de DNA / Sequência de Bases / Regiões Promotoras Genéticas / Adenosina Trifosfatases / Proteínas de Transporte de Cátions / Linhagem Celular Tumoral / ATPases Transportadoras de Cobre / Genética / Degeneração Hepatolenticular / Luciferases Limite: Adolescente / Adulto / Criança / Feminino / Humanos / Masculino Idioma: Chinês Revista: Chinese Journal of Medical Genetics Ano de publicação: 2005 Tipo de documento: Artigo