Regulation of AUXIN RESPONSE FACTOR3 by TAS3 ta-siRNA affects developmental timing and patterning in Arabidopsis.

By Noah Fahlgren, Taiowa A. Montgomery, M. Howell, Edwards Allen, Sarah K. Dvorak, Amanda L. Alexander, James C. Carrington. Current Biology, 2006

600 citations recorded by the source corpus.

Subfields: Molecular Biology, Plant Science

View Paper: https://www.semanticscholar.org/paper/1dd005c3984ec756ccaa333444866d90ed757065

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Citations in the corpus

The control of developmental phase transitions in plants (2011, background): “…the effects of ta-siRNAs on heteroblasty may be limited to their ability to affect leaf polarity via their targeting of auxin response factors (Allen and Howell, 2010; Fahlgren et al., 2006; Hunter et al., 2006; Pekker et al., 2005), the effects of disturbed miRNA biogenesis are more diverse.”
Endogenous siRNA and miRNA targets identified by sequencing of the Arabidopsis degradome. (2008, unknown): “In cases like TAS1a-c and TAS2, for which other factors known to promote secondary siRNA formation, such as multiple miRNA complementary sites [7, 22] or AGO7 dependency [29–32], are not evident, high cleavageproduct accumulation may promote entrance to the secondary siRNA pathway.”
Specificity of ARGONAUTE7-miR390 interaction and dual functionality in TAS3 trans-acting siRNA formation. (2008, background): “…target mRNAs encoding several AUXIN RESPONSE FACTORs (ARF3 and ARF4), negative regulation of which is necessary for proper developmental timing and lateral organ development along the adaxial-abaxial axis (Adenot et al., 2006; Fahlgren et al., 2006; Garcia et al., 2006; Hunter et al., 2006).”
Biosynthesis and Regulation of Phenylpropanoids in Plants (2017, background): “…2007; Montgomery et al., 2008a). ta-siRNAs produced from AtTAS3 is triggered by 21nt miR390-mediated cleavage through “a two-hit trigger model” (Allen et al., 2005; Adenot et al., 2006; Axtell et al., 2006; Fahlgren et al., 2006; Garcia et al., 2006; Howell et al., 2007; Montgomery et al., 2008b).”
A two-hit trigger for siRNA biogenesis in plants. (2006, unknown): “…tasiRNAs from the AtTAS3 locus, required for the proper timing of vegetative development and regulation of organ polarity (Adenot et al., 2006; Fahlgren et al., 2006; Garcia et al., 2006; Hunter et al., 2006), are conserved among diverse flowering plants (Allen et al., 2005; Williams et al.,…”
Small RNAs and Their Roles in Plant Development (2009, background): “The only ta-siRNAs with well-defined biological functions are the tasiR-auxin response factors (ARFs) from the TAS3 locus (Adenot et al. 2006, Fahlgren et al. 2006, Garcia et al. 2006, Hunter et al. 2006).”
Sorting of small RNAs into Arabidopsis argonaute complexes is directed by the 5' terminal nucleotide. (2008, background): “…expression of some members of the ARF gene family to control the vegetative phase transition during Arabidopsis development (Adenot et al., 2006; Fahlgren et al., 2006; Garcia et al., 2006; Hunter et al., 2006). natsiRNAs are derived from natural antisense transcripts. dsRNAs formed by…”
Micro RNAs and Short‐interfering RNAs in Plants (2007, background): “…silencing of transposons and repetitive elements (Zilberman et al. 2003; Chan et al. 2004; Xie et al. 2004), 21-nt tasiRNAs in plant development (Fahlgren et al. 2006; Hunter et al. 2006) and two natsiRNAs implicated in stress responses (Borsani et al. 2005; Katiyar-Agarwal et al. 2006), the…”
A diverse and evolutionarily fluid set of microRNAs in Arabidopsis thaliana. (2006, background): “A segment of the TAS transcript is converted to dsRNA by RDR6, which is then successively cleaved by DCL4 into 21-nt siRNAs that are then loaded into an AGO1- or AGO7-containing silencing complex where they direct cleavage of the mRNA targets (Peragine et al. 2004; Vazquez et al. 2004; Allen et al. ”