AI Article Synopsis

  • A detailed genome assembly of Plantago major was created using advanced sequencing technologies, revealing a genome size of about 671.27 Mb and 31,654 protein-coding genes.
  • Evolutionary analysis indicated that P. major diverged from related species around 62.18 million years ago and underwent two rounds of whole-genome duplication, contributing to its adaptation capabilities.
  • The study found that roots showed high expression of polyphenol biosynthesis genes and specific amino acid biosynthesis genes were induced under nickel stress, which may explain P. major's global distribution and adaptability.

Article Abstract

Plantago is a major genus belonging to the Plantaginaceae family and is used in herbal medicine, functional food, and pastures. Several Plantago species are also characterized by their global distribution, but the mechanism underpinning this is not known. Here, we present a high-quality, chromosome-level genome assembly of Plantago major L., a species of Plantago, by incorporating Oxford Nanopore sequencing and Hi-C technologies. The genome assembly size was approximately 671.27 Mb with a contig N50 length of 31.30 Mb. 31,654 protein-coding genes were identified from the genome. Evolutionary analysis showed that P. major diverged from other Lamiales species at ~62.18 Mya and experienced two rounds of WGD events. Notably, many gene families related to plant acclimation and adaptation expanded. We also found that many polyphenol biosynthesis genes showed high expression patterns in roots. Some amino acid biosynthesis genes, such as those involved in histidine synthesis, were highly induced under metal (Ni) stress that led to the accumulation of corresponding metabolites. These results suggest persuasive arguments for the global distribution of P. major through multiscale analysis. Decoding the P. major genome provides a valuable genomic resource for research on dissecting biological function, molecular evolution, taxonomy, and breeding.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10254747PMC
http://dx.doi.org/10.1093/dnares/dsad013DOI Listing

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