Patterns of Auxin Transport and Gene Expression during Primordium Development Revealed by Live Imaging of the Arabidopsis Inflorescence Meristem
By Marcus Heisler, C. Ohno, P. Das, P. Sieber, G. V. Reddy, Jeff A. Long, Elliot M. Meyerowitz. Current Biology, 2005
1,195 citations recorded by the source corpus.
Subfields: Molecular Biology, Plant Science
View Paper: https://www.semanticscholar.org/paper/e71fb26b4a9e2c996499c0b78df22fad142a768f
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In Molecular Biology
- Jir□í Friml
- Ben Scheres
- René Benjamins
- J. Petrášek
- Maciek Adamowski
- E. Benková
- Ottoline Leyser
- M. Sauer
In Plant Science
- Jir□í Friml
- J. Petrášek
- Ben Scheres
- René Benjamins
- E. Benková
- Maciek Adamowski
- Ottoline Leyser
- M. Sauer
Citations in the corpus
- Control of leaf vascular patterning by polar auxin transport. (2006, positive): “This origin is, in fact, recognizable in the mature pattern of higher leaves, GENES & DEVELOPMENT 1023 where ULDs represent typical third-order connected veins (Kang and Dengler 2004).”
- Auxin: the looping star in plant development. (2008, positive): “PIN1, although quite complex and dynamic, represents the most crucial parameter in the model (53).”
- PIN-Dependent Auxin Transport: Action, Regulation, and Evolution (2015, positive): “In the shoot apical meristem, where these organs originate, PIN1 is expressed in the outermost tissue layer, with polarities converging at an auxin maximum in the primordium tip (Benková et al., 2003; Reinhardt et al., 2003; Heisler et al., 2005; Figures 1A and 1B).”
- Auxin: a trigger for change in plant development. (2009, neutral): “For example, in vivo time-lapse imaging of organ initiation at shoot apical meristems (Heisler et al., 2005) and lateral root organogenesis (Dubrovsky et al.”
- Model for the regulation of Arabidopsis thaliana leaf margin development (2011, positive): “The functional importance of interspersed CUC2 and auxin activity maxima at the leaf margin, together with previous studies (9), suggests the following conceptual model of serration development (Fig.”
- REVIEW: PART OF A SPECIAL ISSUE ON THE PLANT CELL CYCLE Auxin, cytokinin and the control of shoot branching (2011, positive): “An important consideration here is the observation that addition of auxin directly to buds has no effect on bud activation or auxin transport canalization out of the bud, even though it can transcriptionally upregulate PINs (Blilou et al. , 2005; Heisler et al. , 2005; Vieten et al. , 2005).”
- Auxin transport routes in plant development (2009, positive): “…et al., 1999), endoplasmic reticulum-localized Aequorea victoria green fluorescent protein (GFP) (Friml et al., 2003b), and a nucleus-localized version of GFP or the modified yellow fluorescent protein (YFP) version VENUS-N7 (Heisler et al., 2005), to track their activity in plant tissues.”
- The Balance between the MIR164A and CUC2 Genes Controls Leaf Margin Serration in Arabidopsis[W] (2006, positive): “Indeed, it has been suggested that high auxin levels may inhibit CUC2 expression (Vernoux et al., 2000; Heisler et al., 2005).”
- Auxin acts as a local morphogenetic trigger to specify lateral root founder cells (2008, positive): “Taken together with the detection of auxin response maxima correlating with shoot- and root-derived organ initiation in different plant species (5, 6, 7), the results presented here suggest a general, evolutionary conserved auxin-based mechanism for acquisition of founder cell identity in plant orga”
- Auxin–Cytokinin Interaction Regulates Meristem Development (2011, neutral): “Key words: Auxin; cytokinin; interaction; shoot meristem; root meristem; development.”