Yao-Wu Yuan

The catalytic domain of all eukaryotic cut-and-paste transposase superfamilies.

Cut-and-paste DNA transposable elements are major components of eukaryotic genomes and are grouped into superfamilies (e.g., hAT, P) based on sequence similarity of the element-encoded transposase. The transposases from several superfamilies possess a protein domain containing an acidic amino acid triad (DDE or DDD) that catalyzes the “cut and paste” transposition reaction. However, it was unclear whether this domain was shared by the transposases from all superfamilies. Through multiple-alignment of transposase sequences from a diverse collection of previously identified and recently annotated elements from a wide range of organisms, we identified the putative DDE/D triad for all superfamilies. Furthermore, we identified additional highly conserved amino acid residues or motifs within the DDE/D domain that together form a “signature string” that is specific to each superfamily. These conserved residues or motifs were exploited as phylogenetic characters to infer evolutionary relationships among all superfamilies. The phylogenetic analysis revealed three major groups that were not previously discerned and led us to revise the classification of several currently recognized superfamilies. Taking the data together, this study suggests that all eukaryotic cut-and-paste transposable element superfamilies have a common evolutionary origin and establishes a phylogenetic framework for all future cut-and-paste transposase comparisons.

Fine-scale variation in meiotic recombination in Mimulus inferred from population shotgun sequencing

Significance This work characterizes variation in recombination across the genome of a flowering plant in detail using unique population genomic and computational approaches. The resulting recombination map approaches nucleotide-level resolution and advances our understanding of basic properties of recombination, notably the findings of enhanced recombination near starts of genes, varying degrees of intensities of “hotspots,” higher activity in exons than introns, and that a large fraction of the genome appears devoid of any recombination activity. Meiotic recombination rates can vary widely across genomes, with hotspots of intense activity interspersed among cold regions. In yeast, hotspots tend to occur in promoter regions of genes, whereas in humans and mice, hotspots are largely defined by binding sites of the positive-regulatory domain zinc finger protein 9. To investigate the detailed recombination pattern in a flowering plant, we use shotgun resequencing of a wild population of the monkeyflower Mimulus guttatus to precisely locate over 400,000 boundaries of historic crossovers or gene conversion tracts. Their distribution defines some 13,000 hotspots of varying strengths, interspersed with cold regions of undetectably low recombination. Average recombination rates peak near starts of genes and fall off sharply, exhibiting polarity. Within genes, recombination tracts are more likely to terminate in exons than in introns. The general pattern is similar to that observed in yeast, as well as in positive-regulatory domain zinc finger protein 9–knockout mice, suggesting that recombination initiation described here in Mimulus may reflect ancient and conserved eukaryotic mechanisms.

Genetic Dissection of a Major Anthocyanin QTL Contributing to Pollinator-Mediated Reproductive Isolation Between Sister Species of Mimulus

Prezygotic barriers play a major role in the evolution of reproductive isolation, which is a prerequisite for speciation. However, despite considerable progress in identifying genes and mutations responsible for postzygotic isolation, little is known about the genetic and molecular basis underlying prezygotic barriers. The bumblebee-pollinated Mimulus lewisii and the hummingbird-pollinated M. cardinalis represent a classic example of pollinator-mediated prezygotic isolation between two sister species in sympatry. Flower color differences resulting from both carotenoid and anthocyanin pigments contribute to pollinator discrimination between the two species in nature. Through fine-scale genetic mapping, site-directed mutagenesis, and transgenic experiments, we demonstrate that a single-repeat R3 MYB repressor, ROSE INTENSITY1 (ROI1), is the causal gene underlying a major quantitative trait locus (QTL) with the largest effect on anthocyanin concentration and that cis-regulatory change rather than coding DNA mutations cause the allelic difference between M. lewisii and M. cardinalis. Together with the genomic resources and stable transgenic tools developed here, these results suggest that Mimulus is an excellent platform for studying the genetics of pollinator-mediated reproductive isolation and the molecular basis of morphological evolution at the most fundamental level—gene by gene, mutation by mutation.

A molecular phylogeny and classification of Verbenaceae.

UNLABELLED PREMISE OF THE STUDY Verbenaceae consist of trees, shrubs, lianas, and herbs distributed primarily in Latin America, where they occur in a wide array of ecosystems. A second center of diversity exists in Africa. Competing morphology-based classifications that rely on different traits conflict in significant ways. A broad phylogenetic study was undertaken to assess those classifications and to examine the historical geography of the family. • METHODS Analysis of seven chloroplast DNA regions for 109 species, representing all genera except one monotypic genus, provide inference into evolutionary relationships in Verbenaceae. • KEY RESULTS The phylogeny shows that none of the traditional classifications reflect phylogenetic relationships very well. Eight clades are recognized as tribes (Casselieae, Citharexyleae, Duranteae, Lantaneae, Neospartoneae trib. nov., Petreeae, Priveae, and Verbeneae). Two genera, Dipyrena and Rhaphithamnus, remain unplaced in these larger clades. Petreeae, which consist of Neotropical lianas, are sister to the rest of the family. Lantaneae and Verbeneae together form a derived clade that comprises approximately two-thirds of the species in Verbenaceae. • CONCLUSIONS We present a new tribal classification, including one new tribe, Neospartoneae trib. nov., to accommodate three small genera of Argentine species (Diostea, Neosparton, and Lampaya). Phylogenetic inference suggests a South American origin for Verbenaceae, with approximately six colonization events having given rise to the Old World species.

A species-level phylogenetic study of the Verbena complex (Verbenaceae) indicates two independent intergeneric chloroplast transfers.

Two major impediments to infer plant phylogenies at inter- or intra- species level include the lack of appropriate molecular markers and the gene tree/species tree discordance. Both of these problems require more extensive investigations. One of the foci of this study is examining the phylogenetic utility of a combined chloroplast DNA dataset (>5.0kb) of seven non-coding regions, in comparison with that of a large fragment (ca. 3.0kb) of a low-copy nuclear gene (waxy), in a recent, rapidly diversifying group, the Verbena complex. The complex includes three very closely related genera, Verbena (base chromosome number x=7), Glandularia (x=5), and Junellia (x=10), comprising some 150 species distributed predominantly in South and North America. Our results confirm the inadequacy of non-coding cpDNA in resolving relationships among closely related species due to lack of variation, and the great potential of low-copy nuclear gene as source of variation. However, this study suggests that when both cpDNA and nuclear DNA are employed in low-level phylogenetic studies, cpDNA might be very useful to infer organelle evolutionary history (e.g., chloroplast transfer) and more comprehensively understand the evolutionary history of organisms. The phylogenetic framework of the Verbena complex resulted from this study suggests that Junellia is paraphyletic and most ancestral among the three genera; both Glandularia and Verbena are monophyletic and have been derived from within Junellia. Implications of this phylogenetic framework to understand chromosome number evolution and biogeography are discussed. Most interestingly, the comparison of the cpDNA and nuclear DNA phylogenies indicates two independent intergeneric chloroplast transfers, both from Verbena to Glandularia. One is from a diploid North American Verbena species to a polyploid North American Glandularia species. The other is more ancient, from the South American Verbena group to the common ancestor of a major Glandularia lineage, which has radiated subsequently in both South and North America. The commonly assumed introgressive hybridization may not explain the chloroplast transfers reported here. The underlying mechanism remains uncertain.

The pentatricopeptide repeat (PPR) gene family, a tremendous resource for plant phylogenetic studies

* Despite the paramount importance of nuclear gene data in plant phylogenetics, the search for candidate loci is believed to be challenging and time-consuming. Here we report that the pentatricopeptide repeat (PPR) gene family, containing hundreds of members in plant genomes, holds tremendous potential as nuclear gene markers. * We compiled a list of 127 PPR loci that are all intronless and have a single orthologue in both rice (Oryza sativa) and Arabidopsis thaliana. The uncorrected p-distances were calculated for these loci between two Arabidopsis species and among three Poaceae genera. We also selected 13 loci to evaluate their phylogenetic utility in resolving relationships among six Poaceae genera and nine diploid Oryza species. * PPR genes have a rapid rate of evolution and can be best used at intergeneric and interspecific levels. Although with substantial amounts of missing data, almost all individual data sets from the 13 loci generate well-resolved gene trees. * With the unique combination of three characteristics (having a large number of loci with established orthology assessment, being intronless, and being rapidly evolving), the PPR genes have many advantages as phylogenetic markers (e.g. straightforward alignment, minimal effort in generating sequence data, and versatile utilities). We perceive that these loci will play an important role in plant phylogenetics.

The genetic control of flower-pollinator specificity.

The ca. 275,000 species of flowering plants are the result of a recent adaptive radiation driven largely by the coevolution between plants and their animal pollinators. Identification of genes and mutations responsible for floral trait variation underlying pollinator specificity is crucial to understanding how pollinator shifts occur between closely related species. Petunia, Mimulus, and Antirrhinum have provided a high standard of experimental evidence to establish causal links from genes to floral traits to pollinator responses. In all three systems, MYB transcription factors seem to play a prominent role in the diversification of pollinator-associated floral traits.

Bulk Segregant Analysis of an Induced Floral Mutant Identifies a MIXTA-Like R2R3 MYB Controlling Nectar Guide Formation in Mimulus lewisii

The genetic and developmental basis of many ecologically important floral traits (e.g., carotenoid pigmentation, corolla tube structure, nectar volume, pistil and stamen length) remains poorly understood. Here we analyze a chemically induced floral mutant of Mimulus lewisii through bulk segregant analysis and transgenic experiments and identify a MIXTA-like R2R3 MYB gene that controls nectar guide formation in M. lewisii flowers, which involves epidermal cell development and carotenoid pigmentation.

An empirical demonstration of using pentatricopeptide repeat (PPR) genes as plant phylogenetic tools: phylogeny of Verbenaceae and the Verbena complex.

The pentatricopeptide repeat (PPR) gene family, with hundreds of members in land plant genomes, has been recognized as a tremendous resource for plant phylogenetic studies based on publicly available genomic data from model organisms. However, whether this appealing nuclear gene marker system can be readily applied to non-model organisms remains questionable, particularly given the potential uncertainties in designing specific primers to only amplify the locus of interest from the sea of PPR genes. Here we demonstrate empirically the use of PPR genes in the family Verbenaceae and the Verbena complex. We also lay out a general scheme to design locus-specific primers to amplify and sequence PPR genes in non-model organisms. Intergeneric relationships within the family Verbenaceae were fully resolved with strong support. Relationships among the closely related genera within the Verbena complex and among some species groups within each genus were also well resolved, but resolution among very closely related species was limited. Our results suggest that PPR genes can be readily employed in non-model organisms. They may be best used to resolve relationships in a spectrum from among distantly related genera to among not-so-closely related congeneric species, but may have limited use among very closely related species.

Reassignment of Species of Paraphyletic Junellia s. l. to the New Genus Mulguraea (Verbenaceae) and New Circumscription of Genus Junellia: Molecular and Morphological Congruence

Abstract Verbenaceae tribe Verbeneae includes three major genera, Verbena, Glandularia, and Junellia, which form a recently diversified group. Junellia is a South American genus, whereas Verbena and Glandularia are distributed in temperate regions of both South and North America. Seven noncoding chloroplast regions were sequenced including intergenic spacers and/or introns in trnD-trnT, trnS-trnG, trnS-trnfM, trnT-trnL, trnG, trnL, and trnL-trnF; the nuclear ITS and ETS regions were also sequenced. Together with previous studies, these results suggest that Junellia, as traditionally conceived, is a paraphyletic group of two separate clades. Junellia should be restricted to the clade containing the type, J. micrantha, which also includes Glandularia subgenus Paraglandularia and the genus Urbania. Consequently Urbania and Glandularia subgenus Paraglandularia are reduced to synonymy under Junellia, and eight new combinations in Junellia are proposed: Junellia ballsii, J. crithmifolia, J. fasciculata, J. hookeriana, J. lucanensis, J. occulta, J. pappigera and J. origenes. The remaining Junellia species form a monophyletic group here designated as the new genus Mulguraea, with 13 new combinations: Mulguraea arequipense, M. asparagoides, M. aspera var. aspera, M. aspera var. longidentata, M. cedroides, M. cinerascens, M. echegarayi, M. hystrix, M. ligustrina var. ligustrina, M. ligustrina var. lorentzii, M. scoparia, M. tetragonocalyx and M. tridens . Verbena and Glandularia s. s. are both monophyletic based on ETS/ITS data, but neither is monophyletic based on cpDNA data. Relationships within each genus are still not wholly resolved, nevertheless there is evidence that South and North American Verbena might both be monophyletic. Verbena and Glandularia are sister groups, and together they are sister to the reconstituted Junellia. Mulguraea is sister to the group comprising all the three genera, Verbena, Glandularia, and Junellia.