Development of a virus-induced gene-silencing system for functional analysis of the RPS2-dependent resistance signalling pathways in Arabidopsis

Erratum to: Plant Mol Biol (2006) 62: 223–232 DOI 10.1007/s11103-006-9016-z

Due to an unfortunate error, an incorrect version of Fig. 1C has been used in the above mentioned publication. The correct reproduction is published below and should be treated as definitive by the reader.

Fig. 1

Effect of the Agrobacterium strain on VIGS efficiency in Arabidopsis. (C) Confirmation of the PDS gene silencing in leaves showing photo-bleaching phenotype. RT-PCR analysis was conducted using total RNA extracted from leaves, seen in nearly white, of plants inoculated with Agrobacterium GV3101 carrying TRV-PDS and the corresponding non-silenced leaves of the wild type TRV (TRV-00)-infected control plants. Typical PCR products are also shown for ubiquitin, used as an internal standard to correct the quantity, from the same tissues. Lanes 1-5 correspond to products from PCR of cycles 20, 24, 28, 32 and 36, respectively. Lane C represents the negative control, in which the RT reaction mix without reverse transcriptase was used as a template in the reaction