Decoding sORF translation - from small proteins to gene regulation

被引:53
作者
Cabrera-Quio, Luis Enrique [1 ]
Herberg, Sarah [1 ]
Pauli, Andrea [1 ]
机构
[1] Vienna Bioctr VBC, Res Inst Mol Pathol, Vienna, Austria
关键词
Ribosome; short proteins; sORF; translation; translational regulation; uORF; OPEN READING FRAMES; RIBOSOME PROFILING REVEALS; GENOME-WIDE ANALYSIS; MESSENGER-RNA DECAY; NONCODING RNA; IN-VIVO; NUCLEOTIDE RESOLUTION; TRANSCRIPT LEADER; MASS-SPECTROMETRY; INITIATION;
D O I
10.1080/15476286.2016.1218589
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Translation is best known as the fundamental mechanism by which the ribosome converts a sequence of nucleotides into a string of amino acids. Extensive research over many years has elucidated the key principles of translation, and the majority of translated regions were thought to be known. The recent discovery of wide-spread translation outside of annotated protein-coding open reading frames (ORFs) came therefore as a surprise, raising the intriguing possibility that these newly discovered translated regions might have unrecognized protein-coding or gene-regulatory functions. Here, we highlight recent findings that provide evidence that some of these newly discovered translated short ORFs (sORFs) encode functional, previously missed small proteins, while others have regulatory roles. Based on known examples we will also speculate about putative additional roles and the potentially much wider impact that these translated regions might have on cellular homeostasis and gene regulation.
引用
收藏
页码:1051 / 1059
页数:9
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