Comprehensive analysis of microRNA-mRNA co-expression in circadian rhythm
- Authors
- Na, Young-Ji; Sung, Jung Hwan; Lee, Suk Chan; Lee, Young-Ju; Choi, Yeun Joo; Park, Woong-Yang; Shin, Hee Sup; Kim, Ju Han
- Issue Date
- 2009-09-30
- Publisher
- 생화학분자생물학회
- Citation
- Experimental & Molecular Medicine, v.41, no.9, pp.638 - 647
- Abstract
- To investigate the potential role of microRNA (miRNA) in the regulation of circadian rhythm, we performed microarray-based expression profiling study of both miRNA and mRNA in mouse liver for 48 h at 4-hour intervals. Circadian miRNA-mRNA target pair is defined as the pair both elements of which show circadian expression patterns and the sequence-based target relationship of which can be predicted. Circadian initiators, Clock and Bmal1, showed inversely correlated circadian expression patterns against their corresponding miRNAs, miR-181d and miR-191, targeting them. In contrast, circadian suppressors, Per, Cry, Me and Rev-erba, exhibited positively correlated circadian expression patterns to their corresponding miRNAs. Genomic location analysis revealed that intronic region showed higher abundance of cyclic than non-cyclic miRNAs targeting circadian genes while other (i.e., 3'-UTR, exon and intergenic) regions showed no difference. It is suggested that miRNAs are involved in the regulation of peripheral circadian rhythm in mouse liver by modulating Clock:Bmal1 complex. Identifying specific miRNAs and their targets that are critically involved in circadian rhythm will provide a better understanding of the regulation of circadian-clock system.
- Keywords
- GENE-EXPRESSION; CAENORHABDITIS-ELEGANS; TARGETS; MECHANISM; SEQUENCES; PLATFORM; PROTEIN; PERIOD; GENE-EXPRESSION; CAENORHABDITIS-ELEGANS; TARGETS; MECHANISM; SEQUENCES; PLATFORM; PROTEIN; PERIOD; circadian rhythm; gene expression profiling; gene expression regulation; liver; mice; microRNA
- ISSN
- 1226-3613
- URI
- https://pubs.kist.re.kr/handle/201004/132147
- DOI
- 10.3858/emm.2009.41.9.070
- Appears in Collections:
- KIST Article > 2009
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