Oriental lily hybrids engineered to resist aphid attack

Establishing in vitro bulb scale cultures of lily cultivars followed by callusing and regeneration after gene transfer was found to be not very successful in our hands, except for ‘Snow Queen’. Identifying a more generally applicable system to generate callus with the ability to regenerate and amenable to Agrobacterium-mediated gene transfer was the goal of the research described here. Callus was induced on style and filament explants of 26 cultivars of lily. The cultivars were chosen from the hybrid groups longiflorum, asiatics and orientals of the genus Lilium but also interspecific hybrids were represented. Most cultivars were diploids but some were of triploid level and one was tetraploid. In general once callus was induced, it could relatively easily be maintained and propagated for further use. Regeneration was observed on both callus types from all cultivars tested with an efficiency ranging from 40 to 100%. Gene transfer as demonstrated by positive reporter gene uidA activity was found in all cultivars tested. Transgenic plants could be obtained in the first series of transformations and the applicability of a marker-free system was proven in lily. The protocol can now be used for the introduction of genes aiming at conferring resistance to aphids

KORRIGAN1 Interacts Specifically with Integral Components of the Cellulose Synthase Machinery

Cellulose is synthesized by the so called rosette protein complex and the catalytic subunits of this complex are the cellulose synthases (CESAs). It is thought that the rosette complexes in the primary and secondary cell walls each contains at least three different non-redundant cellulose synthases. In addition to the CESA proteins, cellulose biosynthesis almost certainly requires the action of other proteins, although few have been identified and little is known about the biochemical role of those that have been identified. One of these proteins is KORRIGAN (KOR1). Mutant analysis of this protein in Arabidopsis thaliana showed altered cellulose content in both the primary and secondary cell wall. KOR1 is thought to be required for cellulose synthesis acting as a cellulase at the plasma membrane–cell wall interface. KOR1 has recently been shown to interact with the primary cellulose synthase rosette complex however direct interaction with that of the secondary cell wall has never been demonstrated. Using various methods, both in vitro and in planta, it was shown that KOR1 interacts specifically with only two of the secondary CESA proteins. The KOR1 protein domain(s) involved in the interaction with the CESA proteins were also identified by analyzing the interaction of truncated forms of KOR1 with CESA proteins. The KOR1 transmembrane domain has shown to be required for the interaction between KOR1 and the different CESAs, as well as for higher oligomer formation of KOR1