A whole-genome analysis of premature termination codons

被引:11
|
作者
Cirulli, Elizabeth T. [1 ]
Heinzen, Erin L. [1 ]
Dietrich, Fred S. [2 ]
Shianna, Kevin V. [1 ]
Singh, Abanish [1 ]
Maia, Jessica M. [1 ]
Goedert, James J. [3 ]
Goldstein, David B. [1 ]
机构
[1] Duke Univ, Ctr Human Genome Variat, Sch Med, Durham, NC 27708 USA
[2] Duke Univ, Med Ctr, Dept Mol Genet & Microbiol, Durham, NC 27710 USA
[3] US Natl Canc Inst Hlth, Infect & Immunoepidemiol Branch, Div Canc Epidemiol & Genet, Rockville, MD 20852 USA
基金
比尔及梅琳达.盖茨基金会;
关键词
Nonsense-mediated decay; Whole-genome sequencing; RNA-Seq; Premature termination codons; MESSENGER-RNA DECAY; NONSENSE-MEDIATED DECAY; GENE; NMD; POSITION;
D O I
10.1016/j.ygeno.2011.07.001
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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 x 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 x 10(-5)). Additionally, stop colon-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. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:337 / 342
页数:6
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