Ebina Isao, Takemoto-Tsutsumi Mariko, Watanabe Shun, Koyama Hiroaki, Endo Yayoi, Kimata Kaori, Igarashi Takuya, Murakami Karin, Kudo Rin, Ohsumi Arisa, Noh Abdul Latif, Takahashi Hiro, Naito Satoshi, Onouchi Hitoshi
Graduate School of Life Science, Hokkaido University, Sapporo 060-0810, Japan.
Graduate School of Agriculture, Hokkaido University, Sapporo 060-8589, Japan.
Nucleic Acids Res. 2015 Feb 18;43(3):1562-76. doi: 10.1093/nar/gkv018. Epub 2015 Jan 23.
Upstream open reading frames (uORFs) are often found in the 5'-leader regions of eukaryotic mRNAs and can negatively modulate the translational efficiency of the downstream main ORF. Although the effects of most uORFs are thought to be independent of their encoded peptide sequences, certain uORFs control translation of the main ORF in a peptide sequence-dependent manner. For genome-wide identification of such peptide sequence-dependent regulatory uORFs, exhaustive searches for uORFs with conserved amino acid sequences have been conducted using bioinformatic analyses. However, whether the conserved uORFs identified by these bioinformatic approaches encode regulatory peptides has not been experimentally determined. Here we analyzed 16 recently identified Arabidopsis thaliana conserved uORFs for the effects of their amino acid sequences on the expression of the main ORF using a transient expression assay. We identified five novel uORFs that repress main ORF expression in a peptide sequence-dependent manner. Mutational analysis revealed that, in four of them, the C-terminal region of the uORF-encoded peptide is critical for the repression of main ORF expression. Intriguingly, we also identified one exceptional sequence-dependent regulatory uORF, in which the stop codon position is not conserved and the C-terminal region is not important for the repression of main ORF expression.
上游开放阅读框(uORFs)常见于真核生物mRNA的5'前导区,可对下游主要开放阅读框的翻译效率产生负调控作用。尽管大多数uORFs的作用被认为与其编码的肽序列无关,但某些uORFs以肽序列依赖的方式控制主要开放阅读框的翻译。为了在全基因组范围内鉴定此类肽序列依赖的调控uORFs,已利用生物信息学分析对具有保守氨基酸序列的uORFs进行了详尽搜索。然而,通过这些生物信息学方法鉴定出的保守uORFs是否编码调控肽尚未通过实验确定。在此,我们使用瞬时表达分析,分析了16个最近鉴定出的拟南芥保守uORFs的氨基酸序列对主要开放阅读框表达的影响。我们鉴定出5个新的uORFs,它们以肽序列依赖的方式抑制主要开放阅读框的表达。突变分析表明,其中4个uORFs中,uORF编码肽的C末端区域对于抑制主要开放阅读框的表达至关重要。有趣的是,我们还鉴定出一个特殊的序列依赖调控uORF,其终止密码子位置不保守,且C末端区域对抑制主要开放阅读框的表达并不重要。