Gene Expression Regulation by Upstream Open Reading Frames and Human Disease

被引:350
作者
Barbosa, Cristina [1 ,2 ]
Peixeiro, Isabel [1 ,2 ]
Romao, Luisa [1 ,2 ]
机构
[1] Inst Nacl Saude Dr Ricardo Jorge, Dept Genet Humana, Lisbon, Portugal
[2] Univ Lisbon, Fac Ciencias, Ctr Biodivers Funct & Integrat Genom, Lisbon, Portugal
来源
PLOS GENETICS | 2013年 / 9卷 / 08期
关键词
MESSENGER-RNA DECAY; FAMILIAL ESSENTIAL THROMBOCYTHEMIA; BETA-GLOBIN GENE; TRANSLATION INITIATION; POSTTRANSCRIPTIONAL REGULATION; 5'-UNTRANSLATED REGION; DEPENDENT TRANSLATION; NONSENSE MUTATIONS; BASE DELETION; PROTEIN;
D O I
10.1371/journal.pgen.1003529
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Upstream open reading frames (uORFs) are major gene expression regulatory elements. In many eukaryotic mRNAs, one or more uORFs precede the initiation codon of the main coding region. Indeed, several studies have revealed that almost half of human transcripts present uORFs. Very interesting examples have shown that these uORFs can impact gene expression of the downstream main ORF by triggering mRNA decay or by regulating translation. Also, evidence from recent genetic and bioinformatic studies implicates disturbed uORF-mediated translational control in the etiology of many human diseases, including malignancies, metabolic or neurologic disorders, and inherited syndromes. In this review, we will briefly present the mechanisms through which uORFs regulate gene expression and how they can impact on the organism's response to different cell stress conditions. Then, we will emphasize the importance of these structures by illustrating, with specific examples, how disturbed uORF-mediated translational control can be involved in the etiology of human diseases, giving special importance to genotype-phenotype correlations. Identifying and studying more cases of uORF-altering mutations will help us to understand and establish genotype-phenotype associations, leading to advancements in diagnosis, prognosis, and treatment of many human disorders.
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页数:12
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