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124 M.L. Lanteri et al.<br />

9.1.1<br />

Auxins Control Root Development<br />

Hormones are essential players for transmitting information and connecting<br />

the whole plant. The action of hormones involves its perception, initiation<br />

of both specific and nonspecific responses and, finally, the result<br />

of a new steady state of growth and/or metabolic conditions. Among hormones,<br />

auxin plays an important role during plant growth and developmental<br />

processes; therefore, one of the essential aims of plant biologists is<br />

to understand its action, regulation and target molecules. As a critical plant<br />

hormone, auxin modulates diverse processes such as tropic responses to<br />

light and gravity, root and shoot morphogenesis, organ patterning, vascular<br />

development and growth in tissue culture (Davies 1995). Auxin is<br />

known to influence cell division, cell expansion and cell differentiation<br />

and to have a profound influence on root morphology. The control of root<br />

length, the enhancement of lateral root (LR) formation and root hair density,<br />

and the induction of adventitious root development are widely known<br />

auxin-induced processes. Mutants that overproduce auxins tend to have<br />

abundant lateral and adventitious roots (Boerjan et al. 1995; King et al.<br />

1995); conversely, mutants deficient in auxin responses are often characterized<br />

by long primary roots and few LRs (Estelle and Somerville 1987;<br />

Hobbie and Estelle 1995).<br />

Although many tissues can synthesize auxin (Ljung et al. 2001), it is<br />

mainly produced in the shoot apical meristem. It was postulated that the<br />

rate and direction of auxin movement through the cells and finally through<br />

the whole plant is the key fate in auxin-mediated responses (Leyser 1998).<br />

Auxin transport is complex and highly regulated, involving many identified<br />

proteins (Morris 2000). One of the most characteristic features of auxin is<br />

its polar cell-to-cell transport (Jones 1998). Both acropetal (Wilkins and<br />

Scott 1968) and basipetal (Davies and Mitchell 1972) transport occurs in<br />

roots. Opposing directions of auxin transport in roots is achieved by spatial<br />

separation. Chemical and genetic approaches have revealed that transport<br />

of auxin to distant sites is clearly required for normal development<br />

(Friml 2003). For example, indole acetic acid (IAA, the main active auxin<br />

in plants) transport is necessary for proper LR development (Reed et al.<br />

1998; Bhalerao et al. 2002; Casimiro et al. 2001). Recent research suggests<br />

that polar transport of auxin is accomplished via vesicular secretion linked<br />

to endocytotic and recycling processes (Baluska et al. 2003). This would<br />

imply that in addition to the hormone-like and morphogen-like properties,<br />

auxin could also have a neurotransmitter-like behavior (Baluska et al. 2003,<br />

2004). IAA biosynthesis, metabolism and transport are key features to orchestrate<br />

plant development. Moreover, mechanisms downstream of auxin<br />

transport must necessarily transduce the auxin message and be relevant

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