Exhaustive identification of conserved upstream open reading frames with potential translational regulatory functions from animal genomes

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作者
Hiro Takahashi
Shido Miyaki
Hitoshi Onouchi
Taichiro Motomura
Nobuo Idesako
Anna Takahashi
Masataka Murase
Shuichi Fukuyoshi
Toshinori Endo
Kenji Satou
Satoshi Naito
Motoyuki Itoh
机构
[1] Kanazawa University,Graduate School of Medical Sciences
[2] Chiba University,Graduate School of Horticulture
[3] National Cancer Center,Fundamental Innovative Oncology Core Center
[4] Hokkaido University,Graduate School of Agriculture
[5] Belarusian State University of Informatics and Radio Electronics,Faculty of Information Technologies and Control
[6] Chubu University,College of Bioscience and Biotechnology
[7] Kanazawa University,Institute of Medical, Pharmaceutical and Health Sciences
[8] Hokkaido University,Graduate School of Information Science and Technology
[9] Kanazawa University,Faculty of Biological Science and Technology, Institute of Science and Engineering
[10] Hokkaido University,Graduate School of Life Science
[11] Chiba University,Graduate School of Pharmaceutical Science
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摘要
Upstream open reading frames (uORFs) are present in the 5′-untranslated regions of many eukaryotic mRNAs, and some peptides encoded by these regions play important regulatory roles in controlling main ORF (mORF) translation. We previously developed a novel pipeline, ESUCA, to comprehensively identify plant uORFs encoding functional peptides, based on genome-wide identification of uORFs with conserved peptide sequences (CPuORFs). Here, we applied ESUCA to diverse animal genomes, because animal CPuORFs have been identified only by comparing uORF sequences between a limited number of species, and how many previously identified CPuORFs encode regulatory peptides is unclear. By using ESUCA, 1517 (1373 novel and 144 known) CPuORFs were extracted from four evolutionarily divergent animal genomes. We examined the effects of 17 human CPuORFs on mORF translation using transient expression assays. Through these analyses, we identified seven novel regulatory CPuORFs that repressed mORF translation in a sequence-dependent manner, including one conserved only among Eutheria. We discovered a much higher number of animal CPuORFs than previously identified. Since most human CPuORFs identified in this study are conserved across a wide range of Eutheria or a wider taxonomic range, many CPuORFs encoding regulatory peptides are expected to be found in the identified CPuORFs.
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