Improvement of the banana “Musa acuminata” reference sequence using NGS data and semi-automated bioinformatics methods

Recent advances in genomics indicate functional significance of a majority of genome sequences and their long range interactions. As a detailed examination of genome organization and function requires very high quality genome sequence, the objective of this study was to improve reference genome assembly of banana (Musa acuminata)

TARP as immunotherapeutic target in AML expressed in the LSC compartment

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Genome structure and chromosome segregation in triploid interspecific plantain bananas (AAB) and breeding accessions (AAAB)

Many banana cultivars are triploid interspecific hybrids between M. acuminata (Genome A, 2n=22) and M. balbisiana (Genome B, 2n=22). They included the important group of Plantain cooking bananas classified as AAB that account for almost 20% of the bananas produced worldwide. Previous molecular analysis suggested that this group is genetically homogeneous but diversified phenotypically through somatic variations. To progress on the understanding of chromosome composition and segregation of the breeding material used to improve plantain bananas, we performed several analysis based on Genotyping By Sequencing (GBS) technologies. We analyzed the A/B chromosomes composition of a few plantain cultivars and discovered chromosome segments with AAA composition and one entire chromosome with ABB composition instead of the supposed general 'AAB' composition. We compared the global chromosome structure of A and B genomes through the construction a high density M. balbisiana genetic map and its comparison with the M. acuminata reference sequence assembly. We identified a large reciprocal translocation between a region of 0.6Mb at the beginning of chromosome 1 and a 8 Mb region at the end of chromosome 3. We also identified a large inversion of 9Mb within chromosome 5. We analyzed the A/B chromosomes segregation in a progeny from an 'AAAB' tetraploid breeding accession derived from a plantain. We revealed frequent recombination between A and B all along the genomes with a few exceptions. The exceptions consisted in the absence of recombination recorded in the inverted segment between A and B on chromosome 5 and a reduced recombination rate near the translocated regions on chromosome 1 and 3. We also observed 62% of aneuploids in the progeny involving mainly the three chromosomes that differed in their global structure between A and B genomes. Implication of these results on the origin of plantain banana cultivars and on breeding of allopolyploid bananas will be discussed based on the patterns of recombination revealed

A saturated SSR/DArT linkage map of Musa acuminata addressing genome rearrangements among bananas

Background: The 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. Results: An 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. Conclusions: We 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. (Résumé d'auteur