Genome-scale spatiotemporal analysis of Caenorhabditis elegans microRNA promoter activity

• Published in: Genome Research Vol. 18; no. 12; pp. 2005 - 2015
• Main Authors: Martinez, Natalia J, Ow, Maria C, Reece-Hoyes, John S, Barrasa, M Inmaculada, Ambros, Victor R, Walhout, Albertha J M
• Format: Journal Article
• Language: English
• Published: United States Cold Spring Harbor Laboratory Press 01.12.2008
• Subjects: Animals; Animals, Genetically Modified; Blotting, Northern; Caenorhabditis elegans; Caenorhabditis elegans - embryology; Caenorhabditis elegans - genetics; Caenorhabditis elegans - metabolism; Embryo, Nonmammalian; Gene Expression Regulation, Developmental; Genes, Helminth; Genome, Helminth; Green Fluorescent Proteins - metabolism; MicroRNAs; Promoter Regions, Genetic; Protein Processing, Post-Translational; Resource; RNA, Helminth - genetics; Time Factors
• ISSN: 1088-9051; 1549-5469; 1549-5477
• DOI: 10.1101/gr.083055.108

The Caenorhabditis elegans genome encodes more than 100 microRNAs (miRNAs). Genetic analyses of miRNA deletion mutants have only provided limited insights into miRNA function. To gain insight into the function of miRNAs, it is important to determine their spatiotemporal expression pattern. Here, we use miRNA promoters driving the expression of GFP as a proxy for miRNA expression. We describe a set of 73 transgenic C. elegans strains, each expressing GFP under the control of a miRNA promoter. Together, these promoters control the expression of 89 miRNAs (66% of all predicted miRNAs). We find that miRNA promoters drive GFP expression in a variety of tissues and that, overall, their activity is similar to that of protein-coding gene promoters. However, miRNAs are expressed later in development, which is consistent with functions after initial body-plan specification. We find that miRNA members belonging to families are more likely to be expressed in overlapping tissues than miRNAs that do not belong to the same family, and provide evidence that intronic miRNAs may be controlled by their own, rather than a host gene promoter. Finally, our data suggest that post-transcriptional mechanisms contribute to differential miRNA expression. The data and strains described here will provide a valuable guide and resource for the functional analysis of C. elegans miRNAs.