TY - JOUR
T1 - Comprehensive detection of human terminal oligo-pyrimidine (TOP) genes and analysis of their characteristics
AU - Yamashita, Riu
AU - Suzuki, Yutaka
AU - Takeuchi, Nono
AU - Wakaguri, Hiroyuki
AU - Ueda, Takuya
AU - Sugano, Sumio
AU - Nakai, Kenta
N1 - Funding Information:
We thank the members of Dynacom Co. Ltd. for technical supports in the database construction. We also thank Nicolas Sierro for critical reading of the manuscript. Computation time was provided by the Super Computer System, Human Genome Center, Institute of Medical Science, University of Tokyo. This work was supported by Grants-in-Aid for Young Scientists (B) from the Ministry of Education, Science, Sports and Culture of Japan and BIRD of Japan Science and Technology Agency (JST). Funding to pay the Open Access publication charges for this article was provided by Grants-in-Aid for Young Scientists (B) from the Ministry of Education, Science, Sports and Culture of Japan.
PY - 2008/6
Y1 - 2008/6
N2 - Although the knowledge accumulated on the transcriptional regulations of eukaryotes is significant, the knowledge on their translational regulations remains limited. Thus, we performed a comprehensive detection of terminal oligo-pyrimidine (TOP), which is one of the well-characterized cis-regulatory motifs for translational controls located immediately downstream of the transcriptional start sites of mRNAs. Utilizing our precise 5′-end information of the full-length cDNAs, we could screen 1645 candidate TOP genes by position specific matrix search. Among them, not only 75 out of 78 ribosomal protein genes but also eight previously identified non-ribosomal-protein TOP genes were included. We further experimentally validated the translational activities of 83 TOP candidate genes. Clear translational regulations exerted on the stimulation of 12-O-tetradecanoyl-1-phorbol-13-acetate for at least 41 of them was observed, indicating that there should be a few hundreds of human genes which are subjected to regulation at translation levels via TOPs. Our result suggests that TOP genes code not only formerly characterized ribosomal proteins and translation-related proteins but also a wider variety of proteins, such as lysosome-related proteins and metabolism-related proteins, playing pivotal roles in gene expression controls in the majority of cellular mRNAs.
AB - Although the knowledge accumulated on the transcriptional regulations of eukaryotes is significant, the knowledge on their translational regulations remains limited. Thus, we performed a comprehensive detection of terminal oligo-pyrimidine (TOP), which is one of the well-characterized cis-regulatory motifs for translational controls located immediately downstream of the transcriptional start sites of mRNAs. Utilizing our precise 5′-end information of the full-length cDNAs, we could screen 1645 candidate TOP genes by position specific matrix search. Among them, not only 75 out of 78 ribosomal protein genes but also eight previously identified non-ribosomal-protein TOP genes were included. We further experimentally validated the translational activities of 83 TOP candidate genes. Clear translational regulations exerted on the stimulation of 12-O-tetradecanoyl-1-phorbol-13-acetate for at least 41 of them was observed, indicating that there should be a few hundreds of human genes which are subjected to regulation at translation levels via TOPs. Our result suggests that TOP genes code not only formerly characterized ribosomal proteins and translation-related proteins but also a wider variety of proteins, such as lysosome-related proteins and metabolism-related proteins, playing pivotal roles in gene expression controls in the majority of cellular mRNAs.
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U2 - 10.1093/nar/gkn248
DO - 10.1093/nar/gkn248
M3 - Article
C2 - 18480124
AN - SCOPUS:46349099804
SN - 0305-1048
VL - 36
SP - 3707
EP - 3715
JO - Nucleic acids research
JF - Nucleic acids research
IS - 11
ER -