Systemic Signalling in Plant Development


Plants are sessile organisms that communicate extensively with their environment to fine‐tune their growth and development. Perception of environmental stimuli often leads to the production of systemic signals that control the development of distant organs and tissues.

Keywords: signalling; phloem; auxin; florigen; plasmodesmata

Figure 1.

Polar localization of a maize PIN1 auxin efflux transporter homologue. A maize pinformed1 gene was tagged with the yellow fluorescent protein. Localization of the PIN1 efflux carrier at the lower edge of cells in a file in the vascular tissue of a developing leaf is evident, and marks the presumed directional transport of auxin. Image courtesy of Andrea Gallavotti. Bar, 20 μm.

Figure 2.

‘Unloading’ of macromolecules from the phloem into the root apex. In these images, the SUCROSE–H+SYMPORTER2 (SUC2) promoter was used to drive specific expression in phloem companion cells of a cell autonomous GFP (a, ‘GFP‐ER’, localized to the lumen of the endoplasmic reticulum (ER)) or of a cytoplasmic GFP (b). Note that the ER‐localized GFP expression is restricted to the phloem vascular strands, whereas the cytoplasmic GFP exits from the phloem and is transported cell to cell and becomes distributed throughout the root tip. The outline of the root tip in (a) is marked by a white line. Images courtesy of Michelle Cilia.

Figure 3.

Graft transmission of a developmental phenotype in tomato. When normal shoots are grafted on to ‘Mouse ears (Me)’ mutant tomato plants (which have a different leaf shape), ‘mouse ear’‐ shaped leaves start to develop on the normal shoot (marked by ‘*’). This morphological transformation is correlated with movement of the Me mRNA into the normal shoot. See text for details. Reproduced from Plant Cell, 2001, 13:2570 – copyright holder American Society of Plant Biologists.

Figure 4.

Evidence that long‐range transport of auxin regulates apical dominance. In the plant on the left, growth of the axillary buds formed in the axil of each leaf is suppressed. In the middle image, after the shoot apex is removed, these axillary buds start to grow out as leafy shoots. On the right, application of auxin in an agar block to the decapitated shoot is sufficient to suppress growth of the axillary buds.

Figure 5.

Model for the role of FT protein as the systemic flowering signal, florigen. Light period‐induced CONSTANS (CO) expression in the leaf phloem companion cells (CC) activates FLOWERING LOCUS T (FT) expression, and FT protein moves into the sieve elements (SE) and is transported (arrows) to the shoot apex. At the apex, FT protein exits the phloem, and forms a complex with FD, leading to transcriptional activation of the floral meristem identity gene APETALA1 (AP1), and the induction of flowers.



Carlsbecker A and Helariutta Y (2005) Phloem and xylem specification: pieces of the puzzle emerge. Current Opinion in Plant Biology 8(5): 512–517.

Corbesier L, Vincent C, Jang S et al. (2007) FT protein movement contributes to long‐distance signaling in floral induction of Arabidopsis. Science 316(5827): 1030–1033.

Fleming AJ (2006) Plant signalling: the inexorable rise of auxin. Trends in Cell Biology 16(8): 397–402.

Gallagher KL and Benfey PN (2005) Not just another hole in the wall: understanding intercellular protein trafficking. Genes and Development 19(2): 189–195.

Kepinski S and Leyser O (2005) Plant development: auxin in loops. Current Biology 15(6): R208–R210.

Kim M, Canio W, Sharon K and Neelima S (2001) Developmental changes due to long‐distance movement of a homeobox fusion transcript in tomato. Science 293(5528): 287–289.

Leyser O (2005) The fall and rise of apical dominance. Current Opinion in Genetics and Development 15(4): 468–471.

Lough TJ and Lucas WJ (2006) Integrative plant biology: role of phloem long‐distance macromolecular trafficking. Annual Review in Plant Biology 57: 203–232.

Pennisi E (2007) Plant science. Long‐sought plant flowering signal unmasked, again. Science 316(5823): 350–351.

Tamaki S, Matsuo S, Wong HL et al. (2007) Hd3a protein is a mobile flowering signal in rice. Science 316(5827): 1033–1036.

Further Reading

An H, Roussot C, Suárez‐López P et al. (2004) CONSTANS acts in the phloem to regulate a systemic signal that induces photoperiodic flowering of Arabidopsis. Development 131(15): 3615–3626.

Ayre BG and Turgeon R (2004) Graft transmission of a floral stimulant derived from CONSTANS. Plant Physiology 135(4): 2271–2278.

Jackson D (2001) The long and the short of it: signaling development through plasmodesmata. Plant Cell 13(12): 2569–2572.

Nordstrom A, Tarkowski P, Tarkowska R et al. (2004) Auxin regulation of cytokinin biosynthesis in Arabidopsis thaliana: a factor of potential importance for auxin‐cytokinin‐regulated development. Proceedings of the National Academy of Sciences of the USA 101(21): 8039–8044.

Ruiz‐Medrano R, Xoconostle‐Cazares B and Kragler F (2004) The plasmodesmatal transport pathway for homeotic proteins, silencing signals and viruses. Current Opinion in Plant Biology 7(6): 641–650.

Schmitz G and Theres K (2005) Shoot and inflorescence branching. Current Opinion in Plant Biology 8(5): 506–511.

Stahl Y and Simon R (2005) Plant stem cell niches. International Journal of Developmental Biology 49(5–6): 479–489.

Williams L and Fletcher JC (2005) Stem cell regulation in the Arabidopsis shoot apical meristem. Current Opinion in Plant Biology 8(6): 582–586.

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How to Cite close
Jackson, David(Sep 2007) Systemic Signalling in Plant Development. In: eLS. John Wiley & Sons Ltd, Chichester. [doi: 10.1002/9780470015902.a0020127]