Evolutionary history of Primula grandis
Despite the evolutionary importance of supergenes, their properties in polyploids remain unexplored. Polyploid genomes are expected to undergo chromosomal rearrangements and gene losses over time, potentially affecting supergene architecture. The iconic distyly supergene (S-locus), controlling a floral heteromorphism with two self-incompatible morphs, has been well-documented in diploids, but remains unknown in polyploids.Primula, the classic model for distyly since Darwin, is ancestrally diploid and distylous, yet polyploid, homostylous species with a single, self-compatible floral morph evolved repeatedly. The intraspecific loss of distyly is associated with small loss-of-function mutations in the S-locus CYPT gene controlling style length and female self-incompatibility. Over longer timescales, relaxed selection on CYPT should generate greater accumulation of larger mutations, including exon and gene loss. By analyzing the first assembled genome of an allotetraploid, homostylous species (Primula grandis) in a comparative framework, we discovered two, nearly identicalS-locus alleles in the same subgenome, suggesting it originated via inter-specific hybridization between a homostylous and a distylous progenitor. Conformant to predictions from theory, the macroevolutionary loss of distyly coincided with considerable degeneration of CYPT, while otherS-locus genes remained largely unaffected, suggesting the shift to homostyly preceded and facilitated polyploid establishment. At the whole-genome level, we found minimal subgenome dominance — as expected, given the inferred recent origin ofP. grandis— and highly reduced genetic diversity, congruently with its narrow distribution and self-compatibility. This study provides the first comparison of a supergene across ploidy levels and reproductive systems, contributing new knowledge on the previously unknown fate of supergenes in polyploids.
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This submission includes:
out_JBAT_review4.FINAL_22scaf_rename.fa #Genome assembly of both subgenomes (11 chromosomes each)
out_JBAT_review4.FINAL_22scaf_rename.gff3 #Gene annotation in GFF format
out_JBAT_review4.FINAL_22scaf_rename.gtf #Gene annotation in GTF format
out_JBAT_review3_TEs.FINAL.fa.out.gff #Annotation of transposable and repetitive elements for the P. grandis genome
out_JBAT_review4.FINAL_22scaf_rename.longProt.fasta #Protein sequences of all annotated proteins
out_JBAT_review4.FINAL_22scaf_rename.codingseq.fasta #DNA sequences of all annotated genes in the genome