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    Genomics. 2011 Nov;98(5):337-42. doi: 10.1016/j.ygeno.2011.07.001. Epub 2011 Jul 22.

    A whole-genome analysis of premature termination codons.

    Source

    Center for Human Genome Variation, Duke University School of Medicine, Durham, NC 27708, USA.

    Abstract

    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.

    Copyright © 2011 Elsevier Inc. All rights reserved.

    PMID:
    21803148
    [PubMed - indexed for MEDLINE]
    PMCID:
    PMC3282586
    [Available on 2012/11/1]

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