Tissue culture of oil palm : finding the balance between mass propagation and somaclonal variation

The oil palm (Elaeis guineensis Jacq.) is typically propagated in vitro by indirect somatic embryogenesis, a process in which somatic cells of an explant of choice are, via an intermediate phase of callus growth, induced to differentiate into somatic embryos. The architecture of the oil palm, lacking axillary shoots, does not allow for vegetative propagation. Therefore, somatic embryogenesis is the only alternative to seed propagation, which is hampered by long germination times and low germination rates, for the production of planting material. The current oil palm somatic embryogenesis procedure is associated with several difficulties, which are described in this review. The limited availability of explants, combined with low somatic embryo initiation and regeneration rates, necessitate the proliferation of embryogenic structures, increasing the risk for somaclonal variants such as the mantled phenotype. Several ways to improve the efficiency of the tissue culture method and to reduce the risk of somaclonal variation are described. These include the use of alternative explants and propagation techniques, the introduction of specific embryo maturation treatments and the detection of the mantled abnormality in an early stage. These methods have not yet been fully explored and provide interesting research field for the future. The development of an efficient oil palm micropropagation protocol is needed to keep up with the increasing demand for palm oil in a sustainable way. Mass production of selected, high-yielding palms by tissue culture could raise yields on existing plantations, reducing the need for further expansion of the cultivated area, which is often associated with negative environmental impacts

A combinatorial TIR1/AFB–Aux/IAA co-receptor system for differential sensing of auxin

The plant hormone auxin regulates virtually every aspect of plant growth and development. Auxin acts by binding the F-box protein transport inhibitor response 1 (TIR1) and promotes the degradation of the AUXIN/INDOLE-3-ACETIC ACID (Aux/IAA) transcriptional repressors. Here we show that efficient auxin binding requires assembly of an auxin co-receptor complex consisting of TIR1 and an Aux/IAA protein. Heterologous experiments in yeast and quantitative IAA binding assays using purified proteins showed that different combinations of TIR1 and Aux/IAA proteins form co-receptor complexes with a wide range of auxin-binding affinities. Auxin affinity seems to be largely determined by the Aux/IAA. As there are 6 TIR1/AUXIN SIGNALING F-BOX proteins (AFBs) and 29 Aux/IAA proteins in Arabidopsis thaliana, combinatorial interactions may result in many co-receptors with distinct auxin-sensing properties. We also demonstrate that the AFB5–Aux/IAA co-receptor selectively binds the auxinic herbicide picloram. This co-receptor system broadens the effective concentration range of the hormone and may contribute to the complexity of auxin response

Preliminary Report on the Fishes of the Upper Saline River, Polk and Howard Counties, Arkansas, and Observations on Their Relationships with Land Use and Physiochemical Conditions

The Saline River of southwest Arkansas was impounded by Dierks Lake in 1975. Intensive collecting efforts were made in the river system above Dierks Lake during March, April, and May 1980. Collected specimens were compared with ichthyofaunal lists prior to impoundment. Historic occurrants which were not collected include Notropis amnis, Notropis ortenburgeri, Moxostoma duquesnei, Ammocrypta vivax, and Percina copelandi. Additions to the ichthyofaunal list for the drainage include Fundulus notatus, Etheostoma spectabile, and Percina caprodes. The evidence indicates that 33 species representing six families inhabit the system from the headwaters in Polk County, Arkansas, to Dierks Lake, Howard County, Arkansas. Erosion within the basin ranges from 956 kilograms per hectare per year on grassland to 158,263 kilograms per kilometer per year on roadbanks. Excessive levels of fecal coliform bacteria, cadmium, copper, lead, zinc, and sulfates were noted within the system. The relationship of these factors to the ichthyofauna is discussed

The pea branching RMS2 gene encodes the PsAFB4/5 auxin receptor and is involved in an auxin-strigolactone regulation loop

Strigolactones (SLs) are well known for their role in repressing shoot branching. In pea, increased transcript levels of SL biosynthesis genes are observed in stems of highly branched SL deficient (ramosus1 (rms1) and rms5) and SL response (rms3 and rms4) mutants indicative of negative feedback control. In contrast, the highly branched rms2 mutant has reduced transcript levels of SL biosynthesis genes. Grafting studies and hormone quantification led to a model where RMS2 mediates a shoot-to-root feedback signal that regulates both SL biosynthesis gene transcript levels and xylem sap levels of cytokinin exported from roots. Here we cloned RMS2 using synteny with Medicago truncatula and demonstrated that it encodes a putative auxin receptor of the AFB4/5 clade. Phenotypes similar to rms2 were found in Arabidopsis afb4/5 mutants, including increased shoot branching, low expression of SL biosynthesis genes and high auxin levels in stems. Moreover, afb4/5 and rms2 display a specific resistance to the herbicide picloram. Yeast-two-hybrid experiments supported the hypothesis that the RMS2 protein functions as an auxin receptor. SL root feeding using hydroponics repressed auxin levels in stems and down-regulated transcript levels of auxin biosynthesis genes within one hour. This auxin down-regulation was also observed in plants treated with the polar auxin transport inhibitor NPA. Together these data suggest a homeostatic feedback loop in which auxin up-regulates SL synthesis in an RMS2-dependent manner and SL down-regulates auxin synthesis in an RMS3 and RMS4- dependent manner

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