AtPIN4 mediates sink-driven auxin gradients and root patterning in Arabidopsis.

By Jir□í Friml, E. Benková, Ikram Blilou, J. Wiśniewska, Thorsten Hamann, K. Ljung, S. Woody, G. Sandberg, Ben Scheres, G. Jürgens and 1 more. Cell, 2002

877 citations recorded by the source corpus.

Subfields: Molecular Biology, Plant Science

View Paper: https://www.semanticscholar.org/paper/754cd3cfe5deb12cd2bd730daa40fae7ffa3eeaa

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Citations in the corpus

Auxin: a trigger for change in plant development. (2009, neutral): “Once a lateral or primary root meristem becomes functional, a stable auxin gradient forms with its maximum in the quiescent center and young columella cells (Sabatini et al., 1999; Friml et al., 2002a), which is required to maintain the pattern of the root meristem (Blilou et al.”
Comprehending crystalline β-carotene accumulation by comparing engineered cell models and the natural carotenoid-rich system of citrus (2011, neutral): “In particular, AtPIN4 mediates the sink-driven auxin gradients and the resulting auxin maximum in the QC and the columella initial, and it signals the QC to regulate auxin-driven root patterning (Friml et al., 2002).”
Efflux-dependent auxin gradients establish the apical–basal axis of Arabidopsis (2003, background): “For later development, chemical manipulation of auxin distribution has suggested a link between patterning and auxin transpor”
Expression dynamics of WOX genes mark cell fate decisions during early embryonic patterning in Arabidopsis thaliana (2004, background): “The distribution of auxin within the embryo appears to require directional transport involving putative auxin transporters of the PINFORMED (PIN) family (Friml et al., 2002; Gälweiler et al., 1998; Hadfi et al., 1998; Steinmann et al., 1999).”
Auxin control of root development. (2010, background): “…in IAA1/AXR5, IAA3/ SHY2, IAA12/BDL, IAA14/SLR, IAA18/CRANE, IAA19/MSG2, and IAA28 genes lead to plants with altered capacity to form lateral roots (Tian and Reed, 1999; Rogg et al. 2001; Fukaki et al. 2002; Tatematsu et al. 2004; Yang et al. 2004; Uehara et al. 2008; Ploense et al. 2009).”
Root System Architecture from Coupling Cell Shape to Auxin Transport (2008, neutral): “plants, ecotype Col-0, were used for all experiments, including marker lines and auxin transport mutants. The DR5vYFP marker line was generated by fusing DR5rev [”
Flavonoids as Important Molecules of Plant Interactions with the Environment (2014, background): “Additionally, the asymmetric distribution of the PIN-FORMED 1–4 (PIN1–4) auxin efflux proteins surrounding the plasma membrane regions probably contribute to auxin polar transport [149–152].”
Ethylene Regulates Root Growth through Effects on Auxin Biosynthesis and Transport-Dependent Auxin Distribution[W] (2007, neutral): “Formation of the apical hook structure is accompanied by differential auxin responses in hook tissue underlying the asymmetric cell elongation of the hypocotyl (Friml et al., 2002b).”
Auxin biosynthesis by the YUCCA flavin monooxygenases controls the formation of floral organs and vascular tissues in Arabidopsis. (2006, background): “…fate and organ formation in plants are determined by local auxin gradients, which are generated by PIN family proteins that control the directions of auxin flow and overall auxin distribution (Friml et al. 2002, 2003; Benkova et al. 2003; Reinhardt et al. 2003; Heisler et al. 2005; Leyser 2005).”
Antagonistic regulation of PIN phosphorylation by PP2A and PINOID directs auxin flux. (2007, background): “Furthermore, PIN localization can be modulated by environmental (e.g., gravity) or developmental cues (Friml et al., 2002b, 2003; Benková et al., 2003; Reinhardt r Inc. et al., 2003; Scarpella et al., 2006).”