Abstract

Understanding crops genetic diversity and the evolutionary processes that accompanied their worldwide spread is useful for designing effective breeding strategies. Madagascar Island was one of the last major Old World areas where human settlement brought the introduction of Oryza sativa. Early studies in the island had reported the presence of a rice group specific to Madagascar. Using 24 K SNP, we compared diversity patterns at the whole genome and at haplotype (30 SNP-long segments along the genome) levels, between 620 Malagasy and 1929 Asian rice accessions. The haplotype level analysis aimed at identifying local genotypic variations, relative to the whole genome level, using a group assignment method that relies on kernel density estimation in a Principal Component Analysis feature space. Migration bottleneck had resulted in 10–25% reduction of diversity among the Malagasy representatives of indica and japonica populations. Compared to their Asian counterpart, they showed slightly lower indica and japonica introgressions, suggesting the two populations had undergone less recombination when migration to the island occurred. The origins of the Malagasy indica and japonica groups were delineated to indica subpopulation from the Indian subcontinent and to tropical japonica from the Malay Archipelago, respectively. The Malagasy-specific group (Gm) had a rather high gene diversity and an original haplotype pattern: much lower share of indica haplotypes, and much higher share of Aus and japonica haplotypes than indica. Its emergence and expansion are most probably due to inter-group recombination facilitated by sympatry between indica-Aus admixes and “Bulu” type landraces of japonica in the central high plateaux of Madagascar, and to human selection for adaptation to the lowland rice cultivation. Pattern of rice genetic diversity was also tightly associated with the history of human settlement in the island. Emergence of the Gm group is associated with the latest arrivals of Austronesians, who founded the Merina kingdom in the high plateaux and developed lowland rice cultivation. As an intermediary form between Aus, indica and japonica, the three pillars of O. sativa domestication, Gm represents a very valuable genetic resource in breeding for adaptation to cold tolerance in tropical highlands. We proposed the name Rojo for this new rice group.

Highlights

  • Rice, Oryza sativa L., displays very large morphological and physiological variations contributing to its cultivation as a food crop in a very large range of environments (Maclean et al, 2002)

  • The 187 admix accessions, with estimated ancestry coefficients below 0.80, included 90 accessions classified as Admix, Indica subspecies (XI)-adm or Japonica subspecies (GJ)-adm by Wang et al (2018), and 16, 62 and 19 accessions assigned by the same authors to Genetic group including the Aus ecotype (cAus), Genetic group including the Basmati ecotype (cBas) and indica populations, respectively

  • The hypotheses of K = 4 and K = 5 subdivided the indica population into its components XI-1, Indica subpopulation mainly originated from Southeast Asia (XI-3) and Indica subpopulation mainly originated from South Asia (XI-2), and at K = 6, the cBas accessions formed a separate population

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Summary

Introduction

Oryza sativa L., displays very large morphological and physiological variations contributing to its cultivation as a food crop in a very large range of environments (Maclean et al, 2002). This phenotypic diversity is associated with differentiation into two subspecies, indica and japonica (Oka, 1983), and at least two minor ecotypes, Aus and Basmati, distinguishable by isozyme (Glaszmann, 1987) and DNA markers (Garris et al, 2005). The japonica subpopulations named GJ-trop, GJsbtrop and GJ-temp mainly originated from tropical Southeast Asia, subtropical Southeast Asia, and temperate East Asia, respectively. The subpopulations encompassing Aus and Basmati ecotypes were named cAus and cBas, respectively (Wang et al, 2018)

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