Leaf vascular patterning in monocots and dicots
 
Enrico Scarpella1,2,3,*, Danielle Marcos1, Philip Francis1, Annemarie H. Meijer2 and Thomas Berleth1
1 Department. of Botany, University of Toronto , 25 Willcocks Street , Toronto ON , Canada M5S 3B2
2 Institute of Biology, Leiden University , Clusius Laboratory, Wassenaarseweg 64, 2333 AL Leiden , The Netherlands
3 Present address: Department of Biological Sciences, University of Alberta , CW-405 Biological Sciences building, Edmonton AB , Canada T6G 2E9
*email:
 

In leaves, vascular strands of distinct hierarchical orders are organized in closed (i.e. connected) networks. Vascular networks are generated de novo during the development of each leaf primordium. Procambial cells, the precursors of all vascular cells, differentiate from preprocambial cells, which represent a molecularly defined subset of ground meristem cells in the leaf (1).
Mechanisms integrating aligned cell differentiation during vascular strand formation were probably not reinvented in the evolution of leaves, but recruited and revised by leaf-specific controls. In addition, species-specific cues are likely to be involved in leaf vascular patterning, as shown by the successful use of species-specific leaf vascular patterns as taxonomic diagnostic features (2). Whereas most dicot leaves show a ramified pattern of progressively branched veins, most monocot leaves have striate venation patterns in which major veins lie parallel along the proximodistal axis of the leaf and are connected transversely by minor transverse veins (3).
Auxin signals have a profound impact on vascular patterns of dicot leaves. Local auxin application induces the formation of a new vascular strand (4). Further, both defective auxin signal transduction and impaired auxin transport alter leaf vascular patterns in characteristic ways (5-8), and positions of leaf procambium formation are foreshadowed by sites of elevated auxin response (9).
The reduced auxin sensitivity of monocot leaves (10), and their highly reproducible distribution and arrangement of veins (3) suggest that vascular patterns in monocot leaves may be rigidly specified. Recent pharmacological and genetic evidence suggest, however, a role for auxin transport and signal transduction in vascular patterning of monocot leaves (11,12).

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