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STUDY OF THE EXPRESSION AND THE LOCALIZATION POTASSIUM CHANNEL KDC1 DURING PLANT DEVELOPMENT OF CARROT Alex Costa1, Armando Carpaneto2, Serena Varotto3, Elide Formentin1, Oriano Marin1, Mario Terzi1, Franco Gambale2 and Fiorella Lo Schiavo1 1 CRIBI, Centro Interdipartimentale per le Biotecnologie Innovative, Università di Padova, Viale G. Colombo 3, 35121 Padova, Italy;; 2Istituto di Cibernetica e Biofisica-CNR, Via DeMarini 6, 16149 Genova, Italy; 3Dipartimento di Agronomia Ambientale e Produzioni Vegetali, Università di Padova, Agripolis-Via Romea 16, 35020 Legnaro (Padova), Italy The expression pattern of the kdc1 gene, coding for an inwardly directed K+ channel of Daucus carota, is described in several plant tissues and embryo stages. Relative quantitative RT-PCR experiments indicated that the kdc1 transcript is preferentially expressed in plant roots, but is also present in other tissues, and in particular, in the shoot apical meristem. During (somatic) embryonic development, the kdc1 transcript appears as early as the globular stage, and the transcript level remains constant throughout the successive heart and torpedo stages. In situ hybridisation experiments showed that kdc1 mRNA is detectable preferentially in root hairs, root epidermis and endodermis, but is also observed in single cell layers corresponding to L1 (protoderm) of the shoot apical meristem and leaf primordia. In embryos, the hybridisation signal is particularly evident in protoderm cells with a stage dependent expression pattern. Studies with the -glucuronidase promoter confirm preferential expression of kdc1 at the level of embryo protoderm cells and, in plant, in root epidermis and root hairs. Western blot analysis of embryonic proteins and immunolocalisation experiments on somatic embryos sections revealed the presence of KDC1 during embryo development. Patch-clamp experiments, performed on protoplasts isolated from embryos at the torpedo stage demonstrated the presence of two types of functional inward rectifying K+ channels having different amplitudes, kinetics and threshold of current activation. This would be the first case of a plant ionic channel analysed during embryo development