Discovery of imprinted transcripts in the mouse transcriptome using large-scale expression profiling

被引:84
作者
Nikaido, L
Saito, C
Mizuno, Y
Meguro, M
Bono, H
Kadomura, M
Kono, T
Morris, GA
Lyons, PA
Oshimura, M
Hayashizaki, Y
Okazaki, Y
机构
[1] RIKEN, Genom Sci Ctr GSC, Lab Genome Explorat Res Grp, Yokohama Inst,Tsurumi Ku, Yokohama, Kanagawa 2300045, Japan
[2] Yokohama City Univ, Div Genom Informat Resource Explorat, Sci Biol Supramol Syst, Grad Sch Integrated Sci, Yokohama, Kanagawa 2300045, Japan
[3] Tottori Univ, Fac Med, Sch Life Sci, Dept Mol & Cell Genet, Yonago, Tottori 6838503, Japan
[4] Tokyo Univ Agr, Dept Biosci, Tokyo 1568502, Japan
[5] Univ Cambridge, Inst Med Res, JDRF WT, Cambridge CB2 2XY, England
关键词
D O I
10.1101/gr.1055303
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Candidate imprinted transcriptional units in the mouse genome were identified systematically from 27,663 FANTOM2 full-length mouse cDNA clones by expression profiling. Large-scale cDNA microarrays were used to detect differential expression dependent upon chromosomal parent of origin by comparing the mRNA levels in the total tissue of 9.5 dpc parthenogenote and androgenote mouse embryos. Of the FANTOM2 transcripts, 2114 were identified as candidates on the basis of the array data. Of these, 39 mapped to known imprinted regions of the mouse genome, 56 were considered as nonprotein-coding RNAs, and 159 were natural antisense transcripts. The imprinted expression of two transcripts located in the mouse chromosomal region syntenic to the human Prader-Willi syndrome region was confirmed experimentally. We further mapped all candidate imprinted transcripts to the mouse and human genome and were shown in correlation with the imprinting disease loci. These data provide a major resource for understanding the role of imprinting in mammalian inherited traits.
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收藏
页码:1402 / 1409
页数:8
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