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72 P.M. Neumann<br />

resources from mature to young stems that facilitated the maintenance<br />

of growth. Conversely, the fact that a phloem girdle between mature and<br />

young stems inhibited the growth of the young stems reinforces the importance<br />

of phloem transport tissues in interorgan communication. Although<br />

root functioning did not appear to be essentially involved in stem growth<br />

regulation, phloem transport clearly was. The growth regulatory function<br />

of phloem in this case could again be considered analogous to the signaling<br />

facilitated by the nerves of animals. However, the 3-week time scale<br />

required for this shoot growth response to relatively rapid dehydration of<br />

the root environment to become established was totally different from the<br />

seconds required for most animal responses to environmental changes.<br />

5.5<br />

Conclusions and Future Perspectives<br />

Some support is provided in this chapter for the drawing of analogies<br />

between the signaling roles of plant long-distance transport systems and<br />

animal nervous systems. However, the specific findings reviewed here do<br />

not indicate that root apices function as essential neurobiological command<br />

centers involved in regulating shoot growth responses to adverse<br />

changes in the root environment. Cell-to-cell signaling via plasmodesmatal<br />

connections and variations in long-distance transport of hormones,<br />

essential nutrients and water via vascular tissues may conceivably provide<br />

the regulation needed to integrate most higher-plant growth responses to<br />

environmental changes.<br />

<strong>References</strong><br />

Aloni R, Langhans M, Aloni E, Ulrich CI (2004) Role of cytokinin in the regulation of root<br />

gravitropism. Planta 220:177–182<br />

Baluska F, Volkmann D, Barlow PW (2004a) Cell bodies in a cage. Nature 428:371–371<br />

Baluska F, Mancuso S, Volkmann D, Barlow PW (2004b) Root apices as plant command centres:<br />

the unique ‘brain-like’ status of the root apex transition zone. Biologia (Bratislava)<br />

Suppl 59:7–19<br />

Bassani M, Neumann PM, Gepstein S (2004) Differential expression profiles of growthrelated<br />

genes in the elongation zone of maize primary roots. Plant Mol Biol 56:367–380<br />

Birnbaum K, Shasha DE, Wang JY, Jung JW, Lambert GM, Galbraith DW, Benfey PN (2003)<br />

A gene expression map of the Arabidopsis root. Science 302:1956–1960<br />

Chazen O, Hartung W, Neumann PM (1995) The different effects of PEG 6000 and NaCl<br />

on leaf development are associated with differential inhibition of root water transport.<br />

Plant Cell Environ 18:727–735<br />

Chazen O, Neumann PM (1994) Hydraulic signals from the roots and rapid cell wall hardening<br />

in growing maize leaves, are primary responses to PEG induced water deficits.<br />

Plant Physiol 104:1385–139

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