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Bourke, P. M.

Publications and source records attributed to Bourke, P. M..

4 recordsLinked to original sources

Multispecies Mixtures: An Individual-Centered Quantitative Genetic Framework for Complex Plant Neighborhoods

Mixing crop species or varieties in the same field can raise yield and stability, but performance varies widely among combinations that breeders cannot yet predict. What makes a good neighbor is partly heritable, and quantitative genetics models this as an indirect genetic effect describing a genotype's contribution to its neighbors' phenotypes. Here, we extend existing models with a complementary approach based on continuous neighborhoods, in which diverse genotypes of two species are mixed. In a continuous neighborhood design, several genotypes of each species are grown in a single trial, with every plant georeferenced. Each plant's phenotype is decomposed into direct genetic effects, indirect genetic effects from neighbors of both species, and environmental effects. Breeding values are then assembled for each genotype by combining its three genetic effects. We derived analytical expressions for the variances and covariance of these effects, validated the model, and evaluated its statistical properties through simulations spanning a wide range of parameter settings. For the same number of plants, the continuous neighborhood design estimated indirect effects far more accurately than a pairwise design and, in addition, allowed indirect environmental variance to be estimated. Applied to a wheat-alfalfa experiment comprising 3,840 plants, from 181 wheat pure lines and 106 alfalfa families, the model attributed 8.6% and 8.2% of the variance in wheat grain number and alfalfa biomass to direct genetic effects respectively, and 4.0% and 4.6% to indirect genetic effects from alfalfa. The framework therefore offers an individual-entered basis for analyzing multispecies neighborhoods and their breeding potential.

genetics↗

Double Reduction in Allotetraploid Peanut and the Role of Chromosomal Imbalance in Unexpected Linkage Map Artifacts

Polyploidization in peanut (Arachis hypogaea L.) provided evolutionary advantages by increasing heterosis, the response to selection, and enhancing adaptability. However, it also caused a genetic bottleneck by isolating cultivated peanut from its wild diploid relatives. Mechanisms such as homoeologous exchange can partially restore genetic diversity by generating new allelic combinations. Double reduction is a rare segregation pattern restricted to polyploids, in which a single-dosage locus yields duplex gametes. It requires multivalent formation and crossing over between non-sister chromatids, both of which are associated with homoeologous exchange. Although peanut mainly exhibits disomic pairing, occasional multivalents theoretically allow low-frequency double reduction. To estimate double reduction and examine its relationship with genetic instability, a high-density phased linkage map was constructed using a backcross population from a cross between a neoallotetraploid [A. magna K 30097 x A. stenosperma V 15076]4x (MagSten) and cultivated peanut. The final map included 9,717 SNP markers with an average spacing of 0.22 centiMorgans. Some progenies showed unbalanced genomic compositions, creating artifacts in linkage analysis. Removing these progenies improved the map and suggested a common origin for artifacts previously observed in other linkage maps, revealing a novel aspect of mapping in allotetraploid peanut. Analysis of the phased map revealed double reduction in 12% of progenies. Notably, one event produced a genomic composition consistent with theoretical predictions, supporting the expectation that double reduction causes unbalanced genomes in allopolyploids. These results indicate that double reduction is a low but significant frequency genetic phenomenon in the segmental allotetraploid peanut, contributing to the genetic instability and evolutionary dynamics of this and likely other allopolyploid genomes. Article SummaryThis study investigated double reduction, a rare genetic event in segmental allopolyploid peanut, which can create unbalanced genomic compositions and affect genetic diversity. We generated a backcross population using neoallotetraploid and cultivated peanuts, then constructed a high-density phased linkage map. Analysis revealed unbalanced genomic compositions in some progenies caused by homoeologous exchanges, which reduced map quality. Double reduction was estimated to occur in approximately 12% of progenies, aligning with theoretical expectations for genomic imbalance. These results demonstrate that double reduction contributes to genetic instability, inheritance patterns, and genome evolution in allopolyploid organisms such as peanut.

genetics↗

Two high-quality rose genomes underpin a novel Rosa pangenome to advance rose genomics, phylogenetics, and breeding

Rosa, belonging to the family Rosaceae, encompasses more than 150 species which are widely distributed in the northern hemisphere. Renowned for their beauty, roses are cultivated throughout the world for ornamental purposes and the production of essential oils and perfumes. Despite their cultural and commercial significance, the genomic resources of wild Rosa species have not been studied comprehensively, hampering the understanding of their genetic diversity, evolutionary history, and breeding potential. Here we report on high-quality de novo genomes for Rosa sericea and Rosa rugosa. By integrating these two de novo genomes with existing public genomic resources, we have built a Rosaceae panproteome and a Rosa pangenome (spanning wild, traditional garden, and modern rose lineages) using a De Bruijn graph (DBG)-based approach. A maximum likelihood (ML) phylogeny of 18 Rosa haplotypes based on 4,367 single-copy core homology groups (genes) provided robust evolutionary inference, confirming the basal position of R. sericea, and enabled a gene-based macrosynteny analysis across the pangenome. Our analyses revealed significant genomic diversity among species, extensive variation in core gene content, and lineage-specific transposable element (TE) expansion patterns that contribute to the variation in Rosa genome size and to species-specific adaptations. The pangenome also revealed biased diversification of homology groups potentially linked to phenotypic plasticity in Rosa. Specifically, our analysis of the rose scent-related gene family, NUDX1, uncovered its evolutionary trajectory in Rosa, in which TEs insertions provided putative novel regulatory elements that facilitated adaptive evolution in metabolic pathways. This pangenomic study deepens our understanding of the genetic diversity and evolution of traits within the Rosa genus. In addition, the findings lay the foundation for future efforts to understand the genetic mechanisms driving trait evolution, which can support rose breeding.

genomics↗

Detecting quantitative trait loci and exploring chromosomal pairing in autopolyploids using polyqtlR

MotivationThe investigation of quantitative trait loci (QTL) is an essential component in our understanding of how organisms vary phenotypically. However, many important crop species are polyploid (carrying more than two copies of each chromosome), requiring specialised tools for such analyses. Moreover, deciphering meiotic processes at higher ploidy levels is not straightforward, but is necessary to understand the reproductive dynamics of these species, or uncover potential barriers to their genetic improvement. ResultsHere we present polyqtlR, a novel software tool to facilitate such analyses in (auto)polyploid crops. It performs QTL interval mapping in F1 populations of outcrossing polyploids of any ploidy level using identity-by-descent (IBD) probabilities. The allelic composition of discovered QTL can be explored, enabling favourable alleles to be identified and tracked in the population. Visualisation tools within the package facilitate this process, and options to include genetic co-factors and experimental factors are included. Detailed information on polyploid meiosis including prediction of multivalent pairing structures, detection of preferential chromosomal pairing and location of double reduction events can be performed. Availability and implementationpolyqtlR is freely available from the Comprehensive R Archive Network (CRAN) at http://cran.r-project.org/package=polyqtlR. Contactpeter.bourke@wur.nl or chris.maliepaard@wur.nl Supplementary informationSupplementary data are available

genetics↗