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Original multidisciplinary research hereby clarifies the complex geodomestication pathways that generated the vast range of banana cultivars (cvs). Genetic analyses identify the wild ancestors of modern-day cvs and elucidate several key stages of domestication for different cv groups. Archaeology and linguistics shed light on the historical roles of people in the movement and cultivation of bananas from New Guinea to West Africa during the Holocene. The historical reconstruction of domestication processes is essential for breeding programs seeking to diversify and improve banana cvs for the future.plant genetics | historical linguistics | archaeobotany | diploid banana cultivars | triploid banana cultivars N ew multidisciplinary findings from archaeology, genetics, and linguistics clarify the complex geodomestication pathways-the geographical configurations of hybridization and dispersalthat generated the range of modern banana cultivars (cvs). Although recent molecular research, combined with the outcomes of previous genetic studies, elucidates major stages of banana domestication, such as the generation of edible diploids and triploids, it sheds only partial light on the historical and sociospatial contexts of domestication. The geographic distributions of genotypes involved in banana domestication require human translocations of plants, most likely under vegetative forms of cultivation, across vast regions. Linguistic analyses of (traditional) local terms for bananas reveal several striking regional-scale correspondences between genetic and linguistic patterns. These multidisciplinary findings enable the relative dating of the principal events in banana geodomestication and situate banana cultivation within broader sociospatial contexts. Archaeological findings provide a timeline to anchor and calibrate the relative chronology.

Deciphering the diversity of the banana complex needs a joint characterization and analysis of the original wild species and their relatives, primitive diploid forms and triploid derived varieties. Sexuality, the primary source of diversity, is strongly disrupted in the cultivated varieties (sterility, parthenocarpy and vegetative propagation) by human selection of vegetatively maintained punctuated mutations. Many biological tools are available for characterizing this diversity, each one illustrating some peculiar facets, and we show that their joint analysis enables an evolutionary reading of this diversity. We propose various scenarios regarding the structure of wild species, on the domestication of the edible diploids from hybrids between wild forms, on the direct ancestry of triploids from cultivated diploids, and on the ancient migrations dispersing cultivated forms around the world. The comparison with data from archaeology, linguistics and human genetics will enable the validation, refinement and dating of the proposed domestication process.

Background and AimsThe production of triploid banana and plantain (Musa spp.) cultivars with improved characteristics (e.g. greater disease resistance or higher yield), while still preserving the main features of current popular cultivars (e.g. taste and cooking quality), remains a major challenge for Musa breeders. In this regard, breeders require a sound knowledge of the lineage of the current sterile triploid cultivars, to select diploid parents that are able to transmit desirable traits, together with a breeding strategy ensuring final triploidization and sterility. Highly polymorphic single sequence repeats (SSRs) are valuable markers for investigating phylogenetic relationships.MethodsHere, the allelic distribution of each of 22 SSR loci across 561 Musa accessions is analysed.Key Results and ConclusionsWe determine the closest diploid progenitors of the triploid ‘Cavendish’ and ‘Gros Michel’ subgroups, valuable information for breeding programmes. Nevertheless, in establishing the likely monoclonal origin of the main edible triploid banana subgroups (i.e. ‘Cavendish’, ‘Plantain’ and ‘Mutika-Lujugira’), we postulated that the huge phenotypic diversity observed within these subgroups did not result from gamete recombination, but rather from epigenetic regulations. This emphasizes the need to investigate the regulatory mechanisms of genome expression on a unique model in the plant kingdom. We also propose experimental standards to compare additional and independent genotyping data for reference.

BackgroundThe genus Musa is a large species complex which includes cultivars at diploid and triploid levels. These sterile and vegetatively propagated cultivars are based on the A genome from Musa acuminata, exclusively for sweet bananas such as Cavendish, or associated with the B genome (Musa balbisiana) in cooking bananas such as Plantain varieties. In M. acuminata cultivars, structural heterozygosity is thought to be one of the main causes of sterility, which is essential for obtaining seedless fruits but hampers breeding. Only partial genetic maps are presently available due to chromosomal rearrangements within the parents of the mapping populations. This causes large segregation distortions inducing pseudo-linkages and difficulties in ordering markers in the linkage groups. The present study aims at producing a saturated linkage map of M. acuminata, taking into account hypotheses on the structural heterozygosity of the parents.ResultsAn F1 progeny of 180 individuals was obtained from a cross between two genetically distant accessions of M. acuminata, 'Borneo' and 'Pisang Lilin' (P. Lilin). Based on the gametic recombination of each parent, two parental maps composed of SSR and DArT markers were established. A significant proportion of the markers (21.7%) deviated (p < 0.05) from the expected Mendelian ratios. These skewed markers were distributed in different linkage groups for each parent. To solve some complex ordering of the markers on linkage groups, we associated tools such as tree-like graphic representations, recombination frequency statistics and cytogenetical studies to identify structural rearrangements and build parsimonious linkage group order. An illustration of such an approach is given for the P. Lilin parent.ConclusionsWe propose a synthetic map with 11 linkage groups containing 489 markers (167 SSRs and 322 DArTs) covering 1197 cM. This first saturated map is proposed as a "reference Musa map" for further analyses. We also propose two complete parental maps with interpretations of structural rearrangements localized on the linkage groups. The structural heterozygosity in P. Lilin is hypothesized to result from a duplication likely accompanied by an inversion on another chromosome. This paper also illustrates a methodological approach, transferable to other species, to investigate the mapping of structural rearrangements and determine their consequences on marker segregation.

A partial molecular linkage map of the Musa acuminata diploid genome is presented. This map is based on 58 RFLP, four isozyme and 28 RAPD markers segregating in an F2 population of 92 individuals. A total of 90 loci was detected, 77 of which were placed on 15 linkage groups while 13 segregated independently. Segregation distortions were shown by 36% of all loci, mostly favoring the male parent. Chromosome structural rearrangements were believed to be one of the main causes of these distortions. The use of genetic linkage data to further the genetic and evolutionary knowledge of the genus Musa, as well as to help improve the design of breeding strategies, is discussed.

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Understanding of the relations between the components of this complex and identifying their Asian wild relatives and related cultivars will be a valuable asset in breeding programmes and will boost the genetic improvement of East African bananas, but also of other globally important subgroups, in particular the AAA Cavendish.