Temporal regulation of shoot development in Arabidopsis thaliana by miR156 and its target SPL3

By Gang Wu, R. Poethig. Development, 2006

1,087 citations recorded by the source corpus.

Subfields: Molecular Biology, Plant Science

View Paper: https://www.semanticscholar.org/paper/0a01f1333fef0093fb34e77cc497eceef6f55511

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Citations in the corpus

Negative Regulation of Anthocyanin Biosynthesis in Arabidopsis by a miR156-Targeted SPL Transcription Factor[W][OA] (2011, background): “The spl3-1 mutant was identified in the Wassilewskija (Ws) background (Wu and Poethig, 2006). spl3-1 had the same amount of purple pigments in seedlings and inflorescences as wild-type Ws plants (see Supplemental Figure 2 online).”
Target mimicry provides a new mechanism for regulation of microRNA activity (2007, background): “Two examples of miRNAs where overexpression of the wild-type targets has few consequences are miR-156, which targets a series of SPL gene”
Micro RNAs and Short‐interfering RNAs in Plants (2007, background): “2007), whereas the overexpression of SPL3 and an miR156-resistant SPL3, one of the target genes of miR156, results in accelerated flowering (Cardon et al. 1997; Wu and Poethig 2006; Gandikota et al. 2007).”
Plant microRNAs: new players in functional genomics (2013, positive): “The endogenous level of miR156 is temporally regulated, which is very high in the early juvenile vegetative phase but decreases rapidly before the onset of the adult juvenile phase (Wu and Poethig 2006). miR156 also targets spl9 and spl15 genes responsible for shoot maturation (Kantar et al. 2010).”
Complexity of the Alternative Splicing Landscape in Plants[C][W][OPEN] (2013, background): “Members of Squamosa-promoter binding protein like (SPL3, 4, and 5) are key regulators of transition from vegetative to reproductive phase and contain an MBS for miR156 (Wu and Poethig, 2006).”
Temporal analysis of natural variation for the rate of leaf production and its relationship with flowering initiation in Arabidopsis thaliana (2010, background): “Dotted lines correspond to homozygote frequency thresholds (P>0.01), while asterisks indicate markers with higher than expected heterozygosity (P<0.01).”
Uncovering Small RNA-Mediated Responses to Phosphate Deficiency in Arabidopsis by Deep Sequencing1[W][OA] (2009, background): “…induction under 2N. miR156 regulates a group of SQUAMOSA PROMOTER-BINDING PROTEIN-LIKE (SPL) transcription factors involved in juvenile-to-adult vegetative phase transition and other development processes (Wu and Poethig, 2006; Gandikota et al., 2007; Schwarz et al., 2008; Wang et al., 2008).”
Role of miRNAs and siRNAs in biotic and abiotic stress responses of plants (2011, positive): “SBP-LIKE is involved in floral transition and regulation of flowering [125, 126].”
Small RNAs and Their Roles in Plant Development (2009, background): “In Arabidopsis, miR156 targets 11 of the 17 SPL genes; among these genes, SPL3, 4, and 5 promote vegetative phase change as well as floral transition, and SPL9 and SPL15 regulate plastochron length (Schwab et al. 2005, Wang et al. 2008, Wu & Poethig 2006).”
Seasonal and developmental timing of flowering. (2010, background): “Studies of the juvenile to adult phase transition revealed that the role of a particular microRNA, miR156, is to promote the juvenile phase in Arabidopsis and maize, and one consequence of this promotion is to prevent precocious flowering (Wu and Poethig, 2006; Chuck et al., 2007).”
The control of developmental phase transitions in plants (2011, background): “Accordingly, and concomitantly with decreasing miR156 activity, their transcript levels gradually increase during aging (Cardon et al., 1999; Schmid et al., 2005; Wu and Poethig, 2006).”
The sequential action of miR156 and miR172 regulates developmental timing in Arabidopsis. (2009, positive): “In both Arabidopsis and maize, miR156 is highly expressed early in shoot development and decreases with time, while miR172 has the opposite expression pattern (Aukerman and Sakai, 2003; Chuck et al., 2007a; Jung et al., 2007; Lauter et al., 2005; Wu and Poethig, 2006 ).”
Gene silencing in plants using artificial microRNAs and other small RNAs. (2008, background): “At least two Arabidopsis miRNAs, miR172 and miR156, not only cause target RNA cleavage, but also translational inhibition (Aukerman and Sakai, 2003; Chen, 2004; Gandikota et al., 2007; Lauter et al., 2005; Mlotshwa et al., 2006; Schwab et al., 2005; Wu and Poethig, 2006), which is the common mode of”
miR156-regulated SPL transcription factors define an endogenous flowering pathway in Arabidopsis thaliana. (2009, positive): “…ﬂowering, whereas inhibition of miR156 activity, either by mutating its target site in SPL3 ( p35S:rSPL3 ) or through a miR156 target mimic ( p35S:MIM156 ), accelerates ﬂowering (Franco-Zorrilla et al., 2007; Gandikota et al., 2007; Schwab et al., 2005; Wang et al., 2008; Wu and Poethig, 2006).”