Diverged subpopulations in tropicalUrochloa(Brachiaria) forage species indicate a role for facultative apomixis and varying ploidy in their population structure and evolution

Author:

Higgins J1,Tomaszewska P23ORCID,Pellny T K4,Castiblanco V5,Arango J5,Tohme J5,Schwarzacher T2,Mitchell R A4,Heslop-Harrison J S26,De Vega J J1

Affiliation:

1. Earlham Institute, Norwich Research Park , Norwich NR4 7UZ , UK

2. Department of Genetics and Genome Biology, University of Leicester , Leicester LE1 7RH , UK

3. Department of Genetics and Cell Physiology, Faculty of Biological Sciences, University of Wroclaw , 50-328 Wroclaw , Poland

4. Rothamsted Research , Harpenden, Hertfordshire AL5 2JQ , UK

5. International Center for Tropical Agriculture (CIAT) , 6713 Cali , Colombia

6. Key Laboratory of Plant Resources Conservation and Sustainable Utilization/Guangdong Provincial, Key Laboratory of Applied Botany, South China Botanical Garden, Chinese Academy of Sciences , Guangzhou, 510650 , China

Abstract

AbstractBackgroundUrochloa (syn. Brachiaria) is a genus of tropical grasses sown as forage feedstock, particularly in marginal soils. Here we aimed to clarify the genetic diversity and population structure in Urochloa species to understand better how population evolution relates to ploidy level and occurrence of apomictic reproduction.MethodsWe explored the genetic diversity of 111 accessions from the five Urochloa species used to develop commercial cultivars. These accessions were conserved from wild materials collected at their centre of origin in Africa, and they tentatively represent the complete Urochloa gene pool used in breeding programmes. We used RNA-sequencing to generate 1.1 million single nucleotide polymorphism loci. We employed genetic admixture, principal component and phylogenetic analyses to define subpopulations.ResultsWe observed three highly differentiated subpopulations in U. brizantha, which were unrelated to ploidy: one intermixed with U. decumbens, and two diverged from the former and the other species in the complex. We also observed two subpopulations in U. humidicola, unrelated to ploidy; one subpopulation had fewer accessions but included the only characterized sexual accession in the species. Our results also supported a division of U. decumbens between diploids and polyploids, and no subpopulations within U. ruziziensis and U. maxima.ConclusionsPolyploid U. decumbens are more closely related to polyploid U. brizantha than to diploid U. decumbens, which supports the divergence of both polyploid groups from a common tetraploid ancestor and provides evidence for the hybridization barrier of ploidy. The three differentiated subpopulations of apomictic polyploid U. brizantha accessions constitute diverged ecotypes, which can probably be utilized in hybrid breeding. Subpopulations were not observed in non-apomictic U. ruziziensis. Sexual Urochloa polyploids were not found (U. brizantha, U. decumbens) or were limited to small subpopulations (U. humidicola). The subpopulation structure observed in the Urochloa sexual–apomictic multiploidy complexes supports geographical parthenogenesis, where the polyploid genotypes exploit the evolutionary advantage of apomixis, i.e. uniparental reproduction and clonality, to occupy extensive geographical areas.

Funder

Biotechnology and Biological Sciences Research Council

Global Challenge Research Fund

Publisher

Oxford University Press (OUP)

Subject

Plant Science

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