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A whole-genome analysis of premature termination codons.
Cirulli, Elizabeth T; Heinzen, Erin L; Dietrich, Fred S; Shianna, Kevin V; Singh, Abanish; Maia, Jessica M; Goedert, James J; Goldstein, David B.
Afiliación
  • Cirulli ET; Center for Human Genome Variation, Duke University School of Medicine, Durham, NC 27708, USA.
Genomics ; 98(5): 337-42, 2011 Nov.
Article en En | MEDLINE | ID: mdl-21803148
We sequenced the genomes of ten unrelated individuals and identified heterozygous stop codon-gain variants in protein-coding genes: we then sequenced their transcriptomes and assessed the expression levels of the stop codon-gain alleles. An ANOVA showed statistically significant differences between their expression levels (p=4×10(-16)). This difference was almost entirely accounted for by whether the stop codon-gain variant had a second, non-protein-truncating function in or near an alternate transcript: stop codon-gains without alternate functions were generally not found in the cDNA (p=3×10(-5)). Additionally, stop codon-gain variants in two intronless genes were not expressed, an unexpected outcome given previous studies. In this study, stop codon-gain variants were either well expressed in all individuals or were never expressed. Our finding that stop codon-gain variants were generally expressed only when they had an alternate function suggests that most naturally occurring stop codon-gain variants in protein-coding genes are either not transcribed or have their transcripts destroyed.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Genoma Humano / Codón sin Sentido / Desequilibrio Alélico Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Genomics Asunto de la revista: GENETICA Año: 2011 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Genoma Humano / Codón sin Sentido / Desequilibrio Alélico Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Genomics Asunto de la revista: GENETICA Año: 2011 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos