Subgenome dominance shapes novel gene evolution in the decaploid pitcher plant Nepenthes gracilis.
Franziska SaulMathias ScharmannTakanori WakatakeSitaram RajaramanAndré MarquesMatthias FreundGerhard BringmannLouisa ChannonDirk BeckerEmily CarrollYee Wen LowCharlotte LindqvistKadeem J GilbertTanya RennerSachiko MasudaMichaela RichterGerd VoggKen ShirasuTodd P MichaelRainer HedrichVictor A AlbertKenji FukushimaPublished in: Nature plants (2023)
Subgenome dominance after whole-genome duplication generates distinction in gene number and expression at the level of chromosome sets, but it remains unclear how this process may be involved in evolutionary novelty. Here we generated a chromosome-scale genome assembly of the Asian pitcher plant Nepenthes gracilis to analyse how its novel traits (dioecy and carnivorous pitcher leaves) are linked to genomic evolution. We found a decaploid karyotype and a clear indication of subgenome dominance. A male-linked and pericentromerically located region on the putative sex chromosome was identified in a recessive subgenome and was found to harbour three transcription factors involved in flower and pollen development, including a likely neofunctionalized LEAFY duplicate. Transcriptomic and syntenic analyses of carnivory-related genes suggested that the paleopolyploidization events seeded genes that subsequently formed tandem clusters in recessive subgenomes with specific expression in the digestive zone of the pitcher, where specialized cells digest prey and absorb derived nutrients. A genome-scale analysis suggested that subgenome dominance likely contributed to evolutionary innovation by permitting recessive subgenomes to diversify functions of novel tissue-specific duplicates. Our results provide insight into how polyploidy can give rise to novel traits in divergent and successful high-ploidy lineages.
Keyphrases
- genome wide
- copy number
- dna methylation
- poor prognosis
- intellectual disability
- transcription factor
- induced apoptosis
- muscular dystrophy
- palliative care
- genome wide identification
- binding protein
- long non coding rna
- gene expression
- single cell
- cell cycle arrest
- autism spectrum disorder
- cell proliferation
- cell death
- heavy metals
- cell wall