Identification of small ORFs in vertebrates using ribosome footprinting and evolutionary conservation

被引:510
作者
Bazzini, Ariel A. [1 ]
Johnstone, Timothy G. [1 ]
Christiano, Romain [2 ]
Mackowiak, Sebastian D. [3 ]
Obermayer, Benedikt [3 ]
Fleming, Elizabeth S. [1 ]
Vejnar, Charles E. [1 ]
Lee, Miler T. [1 ]
Rajewsky, Nikolaus [3 ]
Walther, Tobias C. [2 ]
Giraldez, Antonio J. [1 ,4 ]
机构
[1] Yale Univ, Sch Med, Dept Genet, New Haven, CT 06510 USA
[2] Yale Univ, Sch Med, Dept Cell Biol, New Haven, CT 06510 USA
[3] Max Delbruck Ctr Mol Med, Berlin, Germany
[4] Yale Univ, Sch Med, Yale Stem Cell Ctr, New Haven, CT USA
基金
瑞士国家科学基金会;
关键词
micropeptides; non-coding RNA; ribosome profiling; small ORFs; translation; OPEN READING FRAMES; POLYCISTRONIC MESSENGER-RNA; LONG NONCODING RNAS; HUMAN GENOME; FUNCTIONAL ELEMENTS; PROVIDES EVIDENCE; TRANSLATION; PEPTIDES; REVEALS; DISCOVERY;
D O I
10.1002/embj.201488411
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
Identification of the coding elements in the genome is a fundamental step to understanding the building blocks of living systems. Short peptides (< 100 aa) have emerged as important regulators of development and physiology, but their identification has been limited by their size. We have leveraged the periodicity of ribosome movement on the mRNA to define actively translated ORFs by ribosome footprinting. This approach identifies several hundred translated small ORFs in zebrafish and human. Computational prediction of small ORFs from codon conservation patterns corroborates and extends these findings and identifies conserved sequences in zebrafish and human, suggesting functional peptide products (micropeptides). These results identify micropeptide-encoding genes in vertebrates, providing an entry point to define their function in vivo.
引用
收藏
页码:981 / 993
页数:13
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