A whole-genome analysis of premature termination codons.
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.
Duke Scholars
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- Transcriptome
- Sequence Alignment
- Polymorphism, Genetic
- Leukocytes, Mononuclear
- Humans
- Genome, Human
- Genetics & Heredity
- Gene Expression Regulation
- Gene Expression Profiling
- DNA, Complementary
Citation
Published In
DOI
EISSN
Publication Date
Volume
Issue
Start / End Page
Location
Related Subject Headings
- Transcriptome
- Sequence Alignment
- Polymorphism, Genetic
- Leukocytes, Mononuclear
- Humans
- Genome, Human
- Genetics & Heredity
- Gene Expression Regulation
- Gene Expression Profiling
- DNA, Complementary