Regulation of Flowering Time and Floral Organ Identity by a MicroRNA and Its APETALA2-Like Target Genes Article, publication date, and citation information can be found at…

By M. Aukerman, H. Sakai. The Plant Cell Online, 2003

1,948 citations recorded by the source corpus.

View Paper: https://www.semanticscholar.org/paper/20ea011e61c18e720a9a0a7c6531e12199f46084

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Citations in the corpus

Micromanagers of gene expression: the potentially widespread influence of metazoan microRNAs (2004, background): “, and the control of leaf and flower development in plant”
Novel and Mechanical Stress–Responsive MicroRNAs in Populus trichocarpa That Are Absent from Arabidopsisw⃞ (2005, background): “, 2005) or, in a few cases, for translational repression (Aukerman and Sakai, 2003; Chen, 2004).”
The Ancestral Developmental Tool Kit of Land Plants (2007, background): “TOE1, TOE2, and AP2 have been shown to play a role in maintaining vegetative growth in Arabidopsis (Aukerman and Sakai 2003; Würschum et al. 2006).”
Origin, biogenesis, and activity of plant microRNAs. (2009, positive): “In those studies where protein production was measured, a discrepancy was observed between the extent of miRNA-directed transcript degradation and the loss of protein accumulation (Aukerman and Sakai, 2003; Bari et al., 2006; Chen, 2003; Gandikota et al., 2007), suggesting that plant miRNAs may also”
Global identification of microRNA–target RNA pairs by parallel analysis of RNA ends (2008, background): “This regulation is exerted by base-pairing to the target mRNA, which directs translational repression or post-transcriptional silencin”
Small RNAs and Their Roles in Plant Development (2009, background): “In Arabidopsis, miR172 promotes flowering by repressing TOE1 and TOE2 (Aukerman & Sakai 2003).”
The sequential action of miR156 and miR172 regulates developmental timing in Arabidopsis. (2009, neutral): “miR172 targets 6 AP2-like genes in Arabidopsis, including TOE1 and TOE2 (Aukerman and Sakai, 2003; Schmid et al., 2003).”
Temporal analysis of natural variation for the rate of leaf production and its relationship with flowering initiation in Arabidopsis thaliana (2010, background): “, 2008) and MIR172 (Aukerman and Sakai, 2003; Wu et al., 2009) that target other genes involved in vegetative phase changes or flowering initiation.”
MicroRNAs as master regulators of the plant NB-LRR defense gene family via the production of phased, trans-acting siRNAs. (2011, neutral): “Consistent with the two-hit model, Medtr2g093060 includes a conserved, cleaved miR172 target site (Aukerman and Sakai 2003), plus a predicted noncleaving and highly degenerate miR156 target site (Fig.”
Small RNAs as big players in plant abiotic stress responses and nutrient deprivation. (2007, background): “Similarly transgenicArabidopsisoverexpressing gibberellin-regulated miR159 and miR319 showed a delayinfloweringtime[69,70].Bycontrast,overexpression of miR172, which targets AP2-type transcription factors, resulted in early flowering [71, 72 ].”
microRNA-mediated repression of rolled leaf1 specifies maize leaf polarity (2004, background): “Long precursor transcripts have recently been identified for MIR-JAW and MIR172a”
DNA methylation mediated by a microRNA pathway. (2010, background): “…miRNAs repress their target gene expression primarily through mRNA cleavage (Llave et al., 2002; Voinnet, 2009), with a subset of them also repressing translation (Aukerman and Sakai, 2003; Brodersen et al., 2008; Chen, 2004; Dugas and Bartel, 2008; Gandikota et al., 2007; Lanet et al., 2009).”