The colorectal microRNAome

被引:748
作者
Cummins, JM
He, YP
Leary, RJ
Pagliarini, R
Diaz, LA
Sjoblom, T
Barad, O
Bentwich, Z
Szafranska, AE
Labourier, E
Raymond, CK
Roberts, BS
Juhl, H
Kinzler, KW
Vogelstein, B [1 ]
Velculescu, VE
机构
[1] Johns Hopkins Univ, Inst Med, Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD 21231 USA
[2] Johns Hopkins Univ, Inst Med, Howard Hughes Med Inst, Baltimore, MD 21231 USA
[3] Rosetta Genom, IL-76706 Rehovot, Israel
[4] Ambion Diagnost, Austin, TX 78744 USA
[5] Rosetta Inpharmat, Seattle, WA 98109 USA
[6] Israelit Hosp, Ctr Canc Res, Indivumed GMBH, D-22297 Hamburg, Germany
关键词
colorectal cancer; dicer; microRNA;
D O I
10.1073/pnas.0511155103
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
MicroRNAs (miRNAs) are a class of small noncoding RNAs that have important regulatory roles in multicellular organisms. The public miRNA database contains 321 human miRNA sequences, 234 of which have been experimentally verified. To explore the possibility that additional miRNAs are present in the human genome, we have developed an experimental approach called miRNA serial analysis of gene expression (miRAGE) and used it to perform the largest experimental analysis of human miRNAs to date. Sequence analysis of 273,966 small RNA tags from human colorectal cells allowed us to identify 200 known mature miRNAs, 133 novel miRNA candidates, and 112 previously uncharacterized miRNA* forms. To aid in the evaluation of candidate miRNAs, we disrupted the Dicer locus in three human colorectal cancer cell lines and examined known and novel miRNAs in these cells. These studies suggest that the human genome contains many more miRNAs than currently identified and provide an approach for the large-scale experimental cloning of novel human miRNAs in human tissues.
引用
收藏
页码:3687 / 3692
页数:6
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