Proceedings of the XLVII Italian
Society of Agricultural Genetics - SIGA Annual Congress
Verona,
Italy - 24/27 September, 2003
ISBN 88-900622-4-X
Poster
Abstract - 4.02
The knotted-like class 1 KNAPE1 of peach is triggered and ectopically
expressed in leaf affected by the curl disease caused by Taphrina deformans
L. Bruno*, D. Giannino**, A.
Chiappetta*, R. Cozza*, A. Tartarini**, D. Mariotti**, A.M. Innocenti*, M.B.
Bitonti*
*)
Università della Calabria, Dipartimento di Ecologia - Laboratorio di
Botanica, Cubo 6B, Arcavacata di Rende, I-87030 Cosenza, Italy
**)
Istituto di Biologia e Biotecnologia Agraria (sez. di Roma), Via Salaria km
29.300, 00016 Monterotondo Scalo (RM)
peach, leaf
curl disease, knotted-like genes class 1, cytokinins
In plants, the
homeobox containing knotted-like genes (KNOX)
class 1 are required for meristem function and determine leaf identity upon
down regulation. Most of KNOX class 1 genes are expressed in the
shoot apical meristem and excluded from leaf primordia. Mutations of these
genes result in a failure to initiate or maintain a SAM, whereas their ectopic
expression alters normal leaf morphology, involving a misbalance of hormone
metabolism. A knotted-like gene was previously isolated and characterised
in peach (KNAPE1) and attributed to class1 on the basis of sequence
homology and meristem specific expression pattern. The triggering of KNAPE1
expression was observed in leaves affected by the curl disease, caused by Taphrina
deformans, a pathogenic fungus which produces auxin and
cytokinin-like compounds. Message localisation was monitored during distinct
stages of disease and the ectopic expression was observed in curly sectors,
corresponding to areas of histological disorder. This pattern is associated
with an indeterminate cell identity, leading to a non coordinate cell
proliferation, which may involve a misbalance and/or misallocation of
cytokinins. Consequently, immunolocalisation of zeatine was performed and
zonation patterns suggest a spatial and temporal relation with the reactivation
of KNAPE1.