Abstract

BackgroundRegulation of gene expression by microRNAs (miRNAs) plays a crucial role in many developmental and physiological processes in plants. miRNAs act to repress expression of their target genes via mRNA cleavage or translational repression. Dozens of miRNA families have been identified in rice, 21 of which are conserved between rice and Arabidopsis. miR172 is a conserved miRNA family which has been shown to regulate expression of APETALA2 (AP2)-like transcription factors in Arabidopsis and maize. The rice genome encodes five AP2-like genes predicted to be targets of miR172. To determine whether these rice AP2-like genes are regulated by miR172 and investigate the function of the target genes, we studied the effect of over-expressing two members of the miR172 family on rice plant development.ResultsAnalysis of miR172 expression showed that it is most highly expressed in late vegetative stages and developing panicles. Analyses of expression of three miR172 targets showed that SUPERNUMERARY BRACT (SNB) and Os03g60430 have high expression in developing panicles. Expression of miR172 was not inversely correlated with expression of its targets although miR172-mediated cleavage of SNB was detected by 5' rapid amplification of cDNA ends (RACE). Over-expression of miR172b in rice delayed the transition from spikelet meristem to floral meristem, and resulted in floral and seed developmental defects, including changes to the number and identity of floral organs, lower fertility and reduced seed weight. Plants over-expressing miR172b not only phenocopied the T-DNA insertion mutant of SNB but showed additional defects in floret development not seen in the snb mutant. However SNB expression was not reduced in the miR172b over-expression plants.ConclusionsThe phenotypes resulting from over-expression of miR172b suggests it represses SNB and at least one of the other miR172 targets, most likely Os03g60430, indicating roles for other AP2-like genes in rice floret development. miR172 and the AP2-like genes had overlapping expression patterns in rice and their expression did not show an obvious negative correlation. There was not a uniform decrease in the expression of the AP2-like miR172 target mRNAs in the miR172b over-expression plants. These observations are consistent with miR172 functioning via translational repression or with expression of the AP2-like genes being regulated by a negative feedback loop.

Highlights

  • Regulation of gene expression by microRNAs plays a crucial role in many developmental and physiological processes in plants. miRNAs act to repress expression of their target genes via messenger RNAs (mRNAs) cleavage or translational repression

  • Arabidopsis miR172 acts as a repressor of the AP2-like genes, TARGET OF EAT 1 (TOE1), TOE2 and TOE3 to promote early flowering [13,20]. miR172-mediated cleavage of mRNAs of these target genes has been detected [21], but there is strong evidence to suggest that the primary mode of repression of these target genes by miR172 is translational inhibition [13,14]

  • Over-expression of miR172b recapitulates the phenotypes of snb and gives rise to additional developmental defects not seen in snb. These results suggest that SUPERNUMERARY BRACT (SNB) and at least one of the other AP2-like target genes are down-regulated in plants over-expressing miR172b, indicating that other members of the AP2-like gene family have roles in rice floret development

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Summary

Introduction

Regulation of gene expression by microRNAs (miRNAs) plays a crucial role in many developmental and physiological processes in plants. miRNAs act to repress expression of their target genes via mRNA cleavage or translational repression. MiRNAs act to repress expression of their target genes via mRNA cleavage or translational repression. MiR172 is a conserved miRNA family which has been shown to regulate expression of APETALA2 (AP2)-like transcription factors in Arabidopsis and maize. MicroRNAs (miRNAs) are regulatory small RNAs that have important roles in regulating development and stress responses in plants [1,2,3,4]. They repress gene expression by targeting cognate messenger RNAs (mRNAs) for cleavage or translational repression [5,6]. The transcription of miR172 target genes is under direct or indirect feedback regulation by their protein products [21]

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