John I. Yoder

Simultaneous amplification of multiple DNA fragments by polymerase chain reaction in the analysis of transgenic plants and their progeny

We describe the simultaneous amplification of different segments of foreign DNA in transgenic plants using the polymerase chain reaction (PCR). We used PCR to simultaneously amplify different regions of transformed T-DNA in order to assay the integrity of transformed constructions in primary tomato transformants. We also used simultaneous PCR amplification to examine the segregation of transformed sequences in progeny of primary transformants. A tomato transformant containing the maize transposable elementAc was crossed to transformants containing the non-autonomousDs1 element flanked by maizeAdh1 sequences. We then ran PCR reactions on DNA from F1 progeny using two sets of primers, one set homologous toAc and one set homologous toAdh1 sequences on either side ofDs1. Because theAc andAdh1 primers resulted in amplification of fragments of different sizes, it was possible to monitor the inheritance ofAc and theDs1 containingAdh1 genein a single reaction. Additionally, it was possible to identify F1 plants in whichDs1 had excised by the amplification of a fragment the size predicted for an empty donor site. In order to run these reactions, we have constructed a simple and inexpensive thermal cycler which, when used in conjunction with the rapid miniscreen plant DNA isolation procedure described, allows the processing of a large number of samples in a single day. Therefore, we have shown that PCR can be a useful tool to monitor the integrity of foreign genes in transgenic plants, to follow the segregation of foreign DNA in progeny, and to assay for the excision of transposable elements.

The evolution of parasitism in plants

The multiple independent origins of plant parasitism suggest that numerous ancestral plant lineages possessed the developmental flexibility to meet the requirements of a parasitic life style, including such adaptations as the ability to recognize host plants, form an invasive haustorium, and regulate the transfer of nutrients and other molecules between two different plants. In this review, we focus on the Orobanchaceae, which are unique among the parasitic plants in that extant member species include the full range of host dependence from facultative to obligate parasites. The recent emergence of genomic resources for these plants should provide new insights into parasitic plant evolution and enable the development of novel genetic strategies for controlling parasitic weeds.

Ac transposition in transgenic tomato plants

SummaryAs an initial step towards developing a transposon mutagenesis system in tomato, the maize transposable element Ac was transformed into tomato plants via Agrobacterium tumefaciens. Southern analysis of leaf tissue indicated that in nine out of eleven transgenic plants, Ac excised from the T-DNA and reintegrated into new chromosomal locations. The comparison of Ac banding pattern in different leaves of the same primary transformant provided evidnece for transposition during later stages of transgenic plant development. There was no evidence of Ds mobilization in tomato transformants.

MOLECULAR SIGNALS AND RECEPTORS: CONTROLLING RHIZOSPHERE INTERACTIONS BETWEEN PLANTS AND OTHER ORGANISMS

Rhizosphere interactions are affected by many different regulatory signals. As yet, however, only a few have been identified. Signals, by definition, contain information, react with a receptor, and elicit a response. Signals may thus represent the highest level of evolved response in rhizosphere communities and, in that sense, occupy a supreme control point. At the same time, some signals may function as modulators of downstream responses, rather than on/off switches. To assess these possibilities, several interactions between plants and soil organisms are described, starting with the molecular interactions between legu- minous plants and symbiotic bacteria of the family Rhizobiaceae, one of the best-charac- terized plant-microbe associations in the rhizosphere. We then examine other interactions between plants and soil organisms for overlap and/or connections with the rhizosphere signals utilized in the legume-Rhizobium symbiosis. Whether information currently avail- able reflects the interaction of the organisms in nature or only in the laboratory has not always been determined. Thus, the key ecological issue of how important some of the signals are under field conditions remains to be addressed. Molecular tools now available make this task less daunting than in the past, and thus a new age of experimental field ecology may soon burst forth in rhizosphere studies. By identifying the signals, receptors, and the critical control points, we can better understand the organismal dynamics in this key belowground ecosystem.

Trans‐specific gene silencing between host and parasitic plants

Species of Orobanchaceae parasitize the roots of nearby host plants to rob them of water and other nutrients. Parasitism can be debilitating to the host plant, and some of the worlds most pernicious agricultural pests are parasitic weeds. We demonstrate here that interfering hairpin constructs transformed into host plants can silence expression of the targeted genes in the parasite. Transgenic roots of the hemi-parasitic plant Triphysaria versicolor expressing the GUS reporter gene were allowed to parasitize transgenic lettuce roots expressing a hairpin RNA containing a fragment of the GUS gene (hpGUS). When stained for GUS activity, Triphysaria roots attached to non-transgenic lettuce showed full GUS activity, but those parasitizing transgenic hpGUS lettuce lacked activity in root tissues distal to the haustorium. Transcript quantification indicated a reduction in the steady-state level of GUS mRNA in Triphysaria when they were attached to hpGUS lettuce. These results demonstrate that the GUS silencing signal generated by the host roots was translocated across the haustorium interface and was functional in the parasite. Movement across the haustorium was bi-directional, as demonstrated in double-junction experiments in which non-transgenic Triphysaria concomitantly parasitized two hosts, one transgenic for hpGUS and the other transgenic for a functional GUS gene. Observation of GUS silencing in the second host demonstrated that the silencing trigger could be moved from one host to another using the parasite as a physiological bridge. Silencing of parasite genes by generating siRNAs in the host provides a novel strategy for controlling parasitic weeds.

Host-plant recognition by parasitic Scrophulariaceae

Parasitic plants in the Scrophulariaceae invade the roots of neighboring plants in order to rob them of water and nutrients. A distinctive feature of these parasites is their ability to cue their development to small molecules released by host-plant roots. Evidence is continuing to emerge that parasite perception of host factors occurs via a redox-associated mechanism. Genes predicted to function during the early stages of parasite-host interactions have been cloned from both plant partners, and their characterization is providing a genetic framework on which to model subterranean plant-plant interactions.

Host plant resistance to parasitic weeds; recent progress and bottlenecks.

Parasitic witchweeds (Striga spp.) and broomrapes (Orobanche and Phelipanche spp.) directly invade the roots of crop plants connecting to the vascular system and abstracting nutrients and water. As a consequence they cause devastating losses in crop yield. Genetic resistance to parasitic weeds is a highly desirable component of any control strategy. Resistance to parasitic plants can occur at different stages of the parasite lifecycle: before attachment to the host, during penetration of the root or after establishment of vascular connections. New studies are beginning to shed light on the molecular mechanisms and signaling pathways involved in plant-plant resistance. The first resistance gene to Striga, encoding a CC-NBS-LRR Resistance protein (R) has been identified and cloned suggesting that host plants resist attack from parasitic plants using similar surveillance mechanisms as those used against fungal and bacterial pathogens. It is becoming clear that the salicylic acid (SA) signaling pathway plays an important role in resistance to parasitic plants and genes encoding pathogenesis-related (PR) proteins are upregulated in a number of the resistant interactions. New strategies for engineering resistance to parasitic plants are also being explored, including the expression of parasite-specific toxins in host roots and RNAi to silence parasite genes crucial for development.

Parasitic plant responses to host plant signals: a model for subterranean plant-plant interactions.

The ability of plants to fulfill nutritional needs by parasitizing neighboring plants has originated several times in angiosperm evolution. Molecular tools are now being exploited to investigate the evolutionary origins of plant parasitism and to dissect the genetic mechanisms governing parasitic plant-host plant interactions. Investigating the nature of signal exchanges between parasitic plants and their hosts serves as a tractable system for understanding how plants in general communicate in the environment. This work should also lead to the development of novel strategies for minimizing the devastation caused by parasitic weeds in international agriculture.

The Parasitic Plant Genome Project: New Tools for Understanding the Biology of Orobanche and Striga

Abstract The Parasitic Plant Genome Project has sequenced transcripts from three parasitic species and a nonparasitic relative in the Orobanchaceae with the goal of understanding genetic changes associated with parasitism. The species studied span the trophic spectrum from free-living nonparasite to obligate holoparasite. Parasitic species used were Triphysaria versicolor, a photosynthetically competent species that opportunistically parasitizes roots of neighboring plants; Striga hermonthica, a hemiparasite that has an obligate need for a host; and Orobanche aegyptiaca, a holoparasite with absolute nutritional dependence on a host. Lindenbergia philippensis represents the closest nonparasite sister group to the parasitic Orobanchaceae and was included for comparative purposes. Tissues for transcriptome sequencing from each plant were gathered to identify expressed genes for key life stages from seed conditioning through anthesis. Two of the species studied, S. hermonthica and O. aegyptiaca, are economically important weeds and the data generated by this project are expected to aid in research and control of these species and their relatives. The sequences generated through this project will provide an abundant resource of molecular markers for understanding population dynamics, as well as provide insight into the biology of parasitism and advance progress toward understanding parasite virulence and host resistance mechanisms. In addition, the sequences provide important information on target sites for herbicide action or other novel control strategies such as trans-specific gene silencing. Nomenclature: Egyptian broomrape, Orobanche aegyptiaca (Pers.) (Syn. Phelipanche aegyptiaca) ORAAE; Lindenbergia philippensis (Cham. & Schltdl.) Benth. LINPH; yellowbeak owls-clover, Triphysaria versicolor (Fisch. & C.A. Mey) TRVEV; purple witchweed, Striga hermonthica, (Del.) Benth. STRHE.

Rapid proliferation of the maize transposable element Activator in transgenic tomato.

We have found that the maize transposable element Activator (Ac) can rapidly proliferate when transformed into tomato plants. The fate of transposed Ac elements in self-pollinated progeny of independent transgenic tomato plants was examined by DNA gel blot hybridizations. When a single copy of Ac was introduced into a transformant, the number of copies usually remained low in subsequent generations. In one lineage, however, the number of Ac elements increased from one to more than 15 copies in only two generations. DNA gel blot analyses indicated that the amplified elements were not grossly rearranged. Amplified copies of Ac resided at unique sites in the genome, and segregation analysis indicated that these sites were not tightly linked at one genetic locus. Taken together, these observations indicate that the mechanism of Ac amplification is associated with transposition.