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SPL genes and other genes involved in flowering, but have no effect on the
expression of miR156 ( Jung et al., 2012, 2011; Wang et al., 2009; Yu et al.,
2012 )( Fig. 5.2 ).
One of the ways in which miR156 represses flowering is through its
effect on miR172, a miRNA that represses several AP2-like transcription
factors that inhibit flowering. High levels of miR172 promote flowering
by repressing the expression of these floral repressors (reviewed in
( Zhu & Helliwell, 2011 ). miR172 is strongly upregulated when adult plants
are transferred from SD to LD ( Jung et al., 2007; Schmid et al., 2003 ), but its
expression also increases early in development in the absence of a LD stim-
ulus ( Wu et al., 2009 ). This early increase in miR172 is complementary
to the decrease in miR156 expression, and is thought to be a consequence
of this decrease because plants overexpressing miR156 have reduced levels
of miR172, whereas plants with reduced levels of miR156 have elevated
levels of mIR172 ( Jung et al., 2011; Wu et al., 2009 ). miR156 represses
miR172 through its effect on the expression of SPL9 , SPL10 , and related
SPL genes. Transgenic plants expressing miR156-resistant SPL9 transcripts
under the regulation of the endogenous SPL9 promoter have elevated
levels of miR172 and flower early ( Wang et al., 2009; Wu et al., 2009 ). This
Adult
Juvenile
miR156
miR156
SPL9 etc
SPL9 etc
miR172b
miR172b
Long days
Long days
AP2-like
AP2-like
GA
GA
SOC1
SOC1
FT
FT
LFY
LFY
FUL
SPL3, 4, 5
FUL
SPL3, 4, 5
AP1
AP1
Flower Flower
Figure 5.2 miR156 controls reproductive competence by repressing the expression of
genes required for flower production. The pathways illustrated here are based on val-
idated miRNA-target interactions and transcription factor binding studies described in
the text. Black indicates genes that are expressed; gray represents repressed genes.
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