Analysis of small human proteins reveals the translation of upstream open reading frames of mRNAs

被引:86
作者
Oyama, M
Itagaki, C
Hata, H
Suzuki, Y
Izumi, T
Natsume, T
Isobe, T
Sugano, S [1 ]
机构
[1] Univ Tokyo, Ctr Human Genome, Minato Ku, Tokyo 1088639, Japan
[2] Univ Tokyo, Div Proteom Res, Minato Ku, Tokyo 1088639, Japan
[3] Univ Tokyo, Inst Med Sci, Div Canc Genom, Minato Ku, Tokyo 1088639, Japan
[4] Natl Inst Adv Ind Sci & Technol, Biol Informat Res Ctr, JBIRC, Koutoh Ku, Tokyo 1350064, Japan
关键词
D O I
10.1101/gr.2384604
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
To find novel short coding sequences from accumulated full-length cDNA sequences, proteomic analysis of small proteins expressed in human leukemia K562 cells was performed using high-resolution nanoflow liquid chromatography coupled with electrospray ionization tandem mass spectrometry. Our analysis led to the identification of 54 proteins not more than 100 amino acids in length, including four novel ones. These novel short coding sequences were all located upstream of the longest open reading frame (ORF) of the corresponding cDNA. Our findings indicate that the translation of short ORFs occurs in vivo whether or not there exists a longer coding region in the downstream of the mRNA. This investigation provides the first direct evidence of translation of upstream ORFs in human cells, which could greatly change the current outline of the human proteome.
引用
收藏
页码:2048 / 2052
页数:5
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