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Comparative genomic analysis of upstream miRNA regulatory motifs in Caenorhabditis.

Authors :
Jovelin R
Krizus A
Taghizada B
Gray JC
Phillips PC
Claycomb JM
Cutter AD
Source :
RNA (New York, N.Y.) [RNA] 2016 Jul; Vol. 22 (7), pp. 968-78. Date of Electronic Publication: 2016 May 02.
Publication Year :
2016

Abstract

MicroRNAs (miRNAs) comprise a class of short noncoding RNA molecules that play diverse developmental and physiological roles by controlling mRNA abundance and protein output of the vast majority of transcripts. Despite the importance of miRNAs in regulating gene function, we still lack a complete understanding of how miRNAs themselves are transcriptionally regulated. To fill this gap, we predicted regulatory sequences by searching for abundant short motifs located upstream of miRNAs in eight species of Caenorhabditis nematodes. We identified three conserved motifs across the Caenorhabditis phylogeny that show clear signatures of purifying selection from comparative genomics, patterns of nucleotide changes in motifs of orthologous miRNAs, and correlation between motif incidence and miRNA expression. We then validated our predictions with transgenic green fluorescent protein reporters and site-directed mutagenesis for a subset of motifs located in an enhancer region upstream of let-7 We demonstrate that a CT-dinucleotide motif is sufficient for proper expression of GFP in the seam cells of adult C. elegans, and that two other motifs play incremental roles in combination with the CT-rich motif. Thus, functional tests of sequence motifs identified through analysis of molecular evolutionary signatures provide a powerful path for efficiently characterizing the transcriptional regulation of miRNA genes.<br /> (© 2016 Jovelin et al.; Published by Cold Spring Harbor Laboratory Press for the RNA Society.)

Details

Language :
English
ISSN :
1469-9001
Volume :
22
Issue :
7
Database :
MEDLINE
Journal :
RNA (New York, N.Y.)
Publication Type :
Academic Journal
Accession number :
27140965
Full Text :
https://doi.org/10.1261/rna.055392.115