The colorectal microRNAome

Jordan M. Cummins(Howard Hughes Medical Institute), Yiping He(Howard Hughes Medical Institute), Rebecca Leary(Howard Hughes Medical Institute), Ray Pagliarini(Howard Hughes Medical Institute), Luis A. Díaz(Howard Hughes Medical Institute), Tobias Sjöblom(Howard Hughes Medical Institute), Omer Barad(Rosetta Genomics (Israel)), Zvi Bentwich(Rosetta Genomics (Israel)), Anna E. Szafranska(PerkinElmer (United States)), Emmanuel Labourier(PerkinElmer (United States)), Christopher K. Raymond(North Seattle College), Brian S. Roberts(North Seattle College), Hartmut Juhl, Kenneth W. Kinzler(Howard Hughes Medical Institute), Bert Vogelstein(Howard Hughes Medical Institute), Victor E. Velculescu(Howard Hughes Medical Institute)
Proceedings of the National Academy of Sciences
February 27, 2006
Cited by 925Open Access
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Abstract

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.


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