Oyama Masaaki, Itagaki Chiharu, Hata Hiroko, Suzuki Yutaka, Izumi Tomonori, Natsume Tohru, Isobe Toshiaki, Sugano Sumio
Human Genome Center, Institute of Medical Science, University of Tokyo, Minato-ku, Tokyo 108-8639, Japan.
Genome Res. 2004 Oct;14(10B):2048-52. doi: 10.1101/gr.2384604.
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.
为了从积累的全长cDNA序列中寻找新的短编码序列,我们利用高分辨率纳流液相色谱与电喷雾电离串联质谱联用技术,对人白血病K562细胞中表达的小蛋白进行了蛋白质组学分析。我们的分析鉴定出了54种长度不超过100个氨基酸的蛋白质,其中包括4种新蛋白。这些新的短编码序列均位于相应cDNA最长开放阅读框(ORF)的上游。我们的研究结果表明,无论mRNA下游是否存在更长的编码区,短ORF的翻译都能在体内发生。这项研究提供了人类细胞中上游ORF翻译的首个直接证据,这可能会极大地改变当前人类蛋白质组的概况。