Secretory RING finger proteins function as effectors in a grapevine galling insect.

BackgroundAll eukaryotes share a conserved network of processes regulated by the proteasome and fundamental to growth, development, or perception of the environment, leading to complex but often predictable responses to stress. As a specialized component of the ubiquitin-proteasome system (UPS), the RING finger domain mediates protein-protein interactions and displays considerable versatility in regulating many physiological processes in plants. Many pathogenic organisms co-opt the UPS through RING-type E3 ligases, but little is known about how insects modify these integral networks to generate novel plant phenotypes.ResultsUsing a combination of transcriptome sequencing and genome annotation of a grapevine galling species, Daktulosphaira vitifoliae, we identified 138 putatively secretory protein RING-type (SPRINGs) E3 ligases that showed structure and evolutionary signatures of genes under rapid evolution. Moreover, the majority of the SPRINGs were more expressed in the feeding stage than the non-feeding egg stage, in contrast to the non-secretory RING genes. Phylogenetic analyses indicated that the SPRINGs formed clusters, likely resulting from species-specific gene duplication and conforming to features of arthropod host-manipulating (effector) genes. To test the hypothesis that these SPRINGs evolved to manipulate cellular processes within the plant host, we examined SPRING interactions with grapevine proteins using the yeast two-hybrid assay. An insect SPRING interacted with two plant proteins, a cellulose synthase, CSLD5, and a ribosomal protein, RPS4B suggesting secretion reprograms host immune signaling, cell division, and stress response in favor of the insect. Plant UPS gene expression during gall development linked numerous processes to novel organogenesis.ConclusionsTaken together, D. vitifoliae SPRINGs represent a novel gene expansion that evolved to interact with Vitis hosts. Thus, a pattern is emerging for gall forming insects to manipulate plant development through UPS targeting

Seed Bank Viability of Inland Saline Wetland Sites in Agro-Ecosystems

Wetland restoration typically includes modifications to soils, flora, and hydrology. Will the return of wetland hydrology to former saline wetlands create conditions suitable for wetland taxa, especially saline wetland indicator species? To answer this question we evaluated the potential restoration efficacy of historical saline wetland soils by re-exposing them to wetland hydrological conditions simulated in a greenhouse. Agricultural lands contained no saline indicator plants and limited wetland species, likely due to significant and long-term land alteration. Restored wetlands showed only a few additional wetland taxa, and seeds of saline wetland plants emerged from soils of only one restored site. Because land alteration threatens the seed bank status of current saline wetlands, potential restoration sites, and even historical saline wetlands under agricultural production in Nebraska, preservation of existing sites that currently have saline dynamics and affluent seed banks may be the only means for continued restoration

Plant manipulation through gall formation constrains amino acid transporter evolution in sap-feeding insects

Abstract Background The herbivore lifestyle leads to encounters with plant toxins and requires mechanisms to overcome suboptimal nutrient availability in plant tissues. Although the evolution of bacterial endosymbiosis alleviated many of these challenges, the ability to manipulate plant nutrient status has evolved in lineages with and without nutritional symbionts. Whether and how these alternative nutrient acquisition strategies interact or constrain insect evolution is unknown. We studied the transcriptomes of galling and free-living aphidomorphs to characterize how amino acid transporter evolution is influenced by the ability to manipulate plant resource availability. Results Using a comparative approach we found phylloxerids retain nearly all amino acid transporters as other aphidomorphs, despite loss of nutritional endosymbiosis. Free living species show more transporters than galling species within the same genus, family, or infraorder, indicating plant hosts influence the maintenance and evolution of nutrient transport within herbivores. Transcript profiles also show lineage specificity and suggest some genes may facilitate life without endosymbionts or the galling lifestyle. Conclusions The transcript abundance profiles we document across fluid feeding herbivores support plant host constraint on insect amino acid transporter evolution. Given amino acid uptake, transport, and catabolism underlie the success of herbivory as a life history strategy, this suggests that plant host nutrient quality, whether constitutive or induced, alters the selective environment surrounding the evolution and maintenance of endosymbiosis

Phylloxerids share ancestral carotenoid biosynthesis genes of fungal origin with aphids and adelgids.

Gene transfer among reproductively isolated organisms can lead to novel phenotypes and increased fitness. Among the Sternorrhyncha, a suborder of plant sap-feeding hemipteran insects, both aphids and adelgids acquired carotenoid biosynthesis genes from a fungal donor that result in ecologically relevant pigmentation. Phylloxerids form another family that are closely related to aphids and adelgids and share similar pigmentation, but are largely uncharacterized for their presence and number of pigment genes that have duplicated among aphids. Here, we examined the transcriptomes of nine phylloxerid species, and performed PCR to amplify carotenoid genes from their genomic DNA. We identified carotenoid cyclase/synthase and desaturase genes in each species and demonstrated that they share the common fungal origin as those of aphids and adelgids based on their exon-intron gene structures and phylogenetic relationships. The phylogenetic analyses also indicated that carotenoid genes evolved following the differentiation of aphids, adelgids, and phylloxerids at the levels of family, genus, and species. Unlike aphids that duplicated these genes in their genomes, phylloxerids maintained only single copies, and some species may lack expression of certain genes. These results suggest that the phylloxerid lifestyle undergoes reduced selection pressure to expand carotenoid synthesis genes, and provides insight into these gene functions in insects

Data from: A global test for phylogenetic signal in shifts in flowering time under climate change

1.Shifts in the timing of flowering are a conspicuous biological signal of climate change. These shifts have been documented across the globe for diverse communities. Although many species are flowering earlier, others have exhibited no shifts or delays in flowering. 2.How species respond phenologically will shape interactions both with other community members and with the abiotic environment, altering fitness, abundance, and ultimately persistence. 3.To understand if variability in phenological response is influenced by evolutionary history, we tested for phylogenetic signal in shifts in flowering onset for thirteen communities representing 116 families across the Northern Hemisphere. We compared the fit of models of neutral evolution (Brownian Motion) with models that incorporate selection (Ornstein-Uhlenbeck). 4.We found significant signal in whether species had shifted and the magnitude of response, with both traits conforming to an Ornstein-Uhlenbeck model of trait evolution. 5.Synthesis. These results show there is global phylogenetic signal in the direction and magnitude of shifts in flowering onset and indicate selection has shaped flowering time responses of related species under climate change; thus, environmentally determined optima may constrain whether and to what degree species respond phenologically to climate change. Our findings further demonstrate the value of testing for phylogenetic signal across multiple communities and comparing multiple models of trait evolution