TY - JOUR
T1 - Comparative analysis of cis-encoded antisense RNAs in eukaryotes
AU - Numata, Koji
AU - Okada, Yuki
AU - Saito, Rintaro
AU - Kiyosawa, Hidenori
AU - Kanai, Akio
AU - Tomita, Masaru
N1 - Funding Information:
We would like to thank Dr. Taishin Kin and Prof. Kiyoshi Asai (Computational Biology Research Center, Advanced Industrial Science and Technology, Japan) for helpful discussions. This research was supported in part by grants from the Non-coding RNA Project by New Energy and Industrial Technology Development Organization (NEDO) of Japan; a Grant-in-Aid for Scientific Research on Priority Areas; and a Grant-in-Aid for the 21st Century Center of Excellence (COE) Program, entitled “Understanding and Control of Life's Function via Systems Biology” (to Keio University, Japan).
PY - 2007/5/1
Y1 - 2007/5/1
N2 - Recent large-scale transcriptomic analyses have identified numerous endogenously encoded cis-antisense RNAs that are thought to play important roles in diverse cellular processes although comprehensive comparative studies among multiple species have yet to be performed. To investigate conserved genomic features across various species that may be related to sense-antisense regulation, we performed comparative analysis of approximately 1000-2000 cis-encoded antisense RNA pairs from five model eukaryotes (Homo sapiens, Mus musculus, Drosophila melanogaster, Arabidopsis thaliana, and Oryza sativa). Analysis of overlapping patterns relative to the exon-intron structure revealed that the number of pairs sharing the 3′ part of the transcripts was larger than that of the 5′-sharing pairs except in rice. Moreover, most of the well-conserved sense-antisense pairs between human and mouse exhibited 3′-overlaps, suggesting that regulatory mechanisms involving these regions may be important in sense-antisense transcription. Functional classification using Gene Ontology revealed that genes related to catalytic activity, nucleotide binding, DNA metabolism, and mitochondria were preferentially distributed within the set of exon-overlapping sense-antisense genes compared to the non-exon-overlapping group in animals. Despite the numerous sense-antisense pairs identified in human and mouse individually, the number of conserved pairs was extremely small (6.6% of the entire set). Whereas both genes of most of the conserved sense-antisense pairs had protein-coding potential, nearly half of the non-conserved pairs included a non-coding RNA, suggesting that non-coding sense-antisense RNAs may function in species-specific regulatory pathways.
AB - Recent large-scale transcriptomic analyses have identified numerous endogenously encoded cis-antisense RNAs that are thought to play important roles in diverse cellular processes although comprehensive comparative studies among multiple species have yet to be performed. To investigate conserved genomic features across various species that may be related to sense-antisense regulation, we performed comparative analysis of approximately 1000-2000 cis-encoded antisense RNA pairs from five model eukaryotes (Homo sapiens, Mus musculus, Drosophila melanogaster, Arabidopsis thaliana, and Oryza sativa). Analysis of overlapping patterns relative to the exon-intron structure revealed that the number of pairs sharing the 3′ part of the transcripts was larger than that of the 5′-sharing pairs except in rice. Moreover, most of the well-conserved sense-antisense pairs between human and mouse exhibited 3′-overlaps, suggesting that regulatory mechanisms involving these regions may be important in sense-antisense transcription. Functional classification using Gene Ontology revealed that genes related to catalytic activity, nucleotide binding, DNA metabolism, and mitochondria were preferentially distributed within the set of exon-overlapping sense-antisense genes compared to the non-exon-overlapping group in animals. Despite the numerous sense-antisense pairs identified in human and mouse individually, the number of conserved pairs was extremely small (6.6% of the entire set). Whereas both genes of most of the conserved sense-antisense pairs had protein-coding potential, nearly half of the non-conserved pairs included a non-coding RNA, suggesting that non-coding sense-antisense RNAs may function in species-specific regulatory pathways.
KW - Full-length cDNA
KW - Naturally occurring sense-antisense RNAs
KW - Non-coding RNA
KW - Transcriptome
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U2 - 10.1016/j.gene.2006.12.005
DO - 10.1016/j.gene.2006.12.005
M3 - Article
C2 - 17250976
AN - SCOPUS:33947604744
SN - 0378-1119
VL - 392
SP - 134
EP - 141
JO - Gene
JF - Gene
IS - 1-2
ER -