Five-needle pines are important forest species that have been devastated by white pine blister rust (WPBR, caused by Cronartium ribicola) across North America. Currently little transcriptomic and genomic data are available to understand molecular interactions in the WPBR pathosystem.
Damage or mortality from pathogens can reduce productivity of forest plantations, as well as significantly harm natural forest ecosystems. Genetic resistance within the host species is the first line of defense for tree species. Resistance breeding programs for the native fusiform rust and exotic (to North America) white pine blister rust diseases are two of the longest concerted efforts in forest trees, spanning more than 50 years. Advances in developing greater genetic resistance have been made in both pathosystems, but unique challenges and opportunities in each system translate to different approaches. Fusiform rust resistance programs have mainly emphasized complete resistance, while partial resistance plays a prominent role in white pine blister rust resistance programs. Advances in the development of molecular genetic tools now permit investigations in conifers and their associated rust pathogens. Good progress has been made in identifying resistant populations and understanding resistance in these pathosystems, and resistant stock is now being used extensively for reforestation and restoration. These programs represent great success stories brought to fruition by the long-term efforts. However, continued support will be needed to enhance the level and fully realize the potential of durable genetic resistance in these invaluable North American conifer species.
The WRKY gene family represents an ancient and highly complex group of transcription factors involved in signal transduction pathways of numerous plant developmental processes and host defense response. Up to now, most WRKY proteins have been identified in a few angiosperm species. Identification of WRKY genes in a conifer species would facilitate a comprehensive understanding of the evolutionary and function-adaptive process of this superfamily in plants. We performed PCR on genomic DNA to clone WRKY sequences from western white pine ( Pinus monticola ), one of the most valuable conifer species endangered by white pine blister rust ( Cronartium ribicola ). In total, 83 P. monticola WRKY (PmWRKY) sequences were identified using degenerate primers targeted to the WRKY domain. A phylogenetic analysis revealed that PmWRKY members fell into four major groups (1, 2a+2b, 2c, and 2d+2e) described in Arabidopsis and rice. Because of high genetic diversity of the PmWRKY family, a modified AFLP method was used to detect DNA polymorphism of this gene family. Polymorphic fragments accounted for 17%–35% of total PCR products in the AFLP profiles. Among them, one WRKY AFLP marker was linked to the major resistance gene (Cr2) against C. ribicola. The results of this study provide basic genomic information for a conifer WRKY gene family, which will pave the way for elucidating gene evolutionary mechanisms in plants and unveiling the precise roles of PmWRKY in conifer development and defense response.