Evolutionary acquisition of promoterassociated non-coding RNA (pancRNA) repertoires diversifies species-dependent gene activation mechanisms in mammals

被引:18
|
作者
Uesaka, Masahiro [1 ,2 ,3 ,5 ]
Agata, Kiyokazu [2 ,3 ,6 ]
Oishi, Takao [4 ]
Nakashima, Kinichi [1 ]
Imamura, Takuya [1 ,2 ,3 ]
机构
[1] Kyushu Univ, Grad Sch Med Sci, Dept Stem Cell Biol & Med, Fukuoka 8128582, Japan
[2] Kyoto Univ, Grad Sch Sci, Dept Biophys, Kyoto 6068502, Japan
[3] Kyoto Univ, Grad Sch Sci, Global COE Program, Kyoto 6068502, Japan
[4] Kyoto Univ, Primate Res Inst, Dept Cellular & Mol Biol, Inuyama, Aichi 4848506, Japan
[5] Univ Tokyo, Grad Sch Sci, Dept Biol Sci, Tokyo 1138654, Japan
[6] Gakushuin Univ, Grad Sch Sci, Dept Life Sci, Grad Course Life Sci,Fac Sci, Tokyo 1718588, Japan
来源
BMC GENOMICS | 2017年 / 18卷
关键词
Long non-coding RNA; Species diversity; Epigenetic regulation; Evolution; CIS-REGULATORY MUTATIONS; BIDIRECTIONAL PROMOTERS; MORPHOLOGICAL EVOLUTION; HUMAN-CELLS; CPG ISLAND; EXPRESSION; GENOME; TRANSCRIPTION; MOUSE; CHROMATIN;
D O I
10.1186/s12864-017-3662-1
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: Recent transcriptome analyses have shown that long non-coding RNAs (ncRNAs) play extensive roles in transcriptional regulation. In particular, we have reported that promoter-associated ncRNAs (pancRNAs) activate the partner gene expression via local epigenetic changes. Results: Here, we identify thousands of genes under pancRNA-mediated transcriptional activation in five mammalian species in common. In the mouse, 1) pancRNA-partnered genes confined their expression pattern to certain tissues compared to pancRNA-lacking genes, 2) expression of pancRNAs was significantly correlated with the enrichment of active chromatin marks, H3K4 trimethylation and H3K27 acetylation, at the promoter regions of the partner genes, 3) H3K4me1 marked the pancRNA-partnered genes regardless of their expression level, and 4) C-or G-skewed motifs were exclusively overrepresented between-200 and-1 bp relative to the transcription start sites of the pancRNA-partnered genes. More importantly, the comparative transcriptome analysis among five different mammalian species using a total of 25 counterpart tissues showed that the overall pancRNA expression profile exhibited extremely high species-specificity compared to that of total mRNA, suggesting that interspecies difference in pancRNA repertoires might lead to the diversification of mRNA expression profiles. Conclusions: The present study raises the interesting possibility that the gain and/or loss of gene-activation-associated pancRNA repertoires, caused by formation or disruption of the genomic GC-skewed structure in the course of evolution, finely shape the tissue-specific pattern of gene expression according to a given species.
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页数:13
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