4.8 Article

Deeply Altered Genome Architecture in the Endoparasitic Flowering Plant Sapria himalayana Griff. (Rafflesiaceae)

期刊

CURRENT BIOLOGY
卷 31, 期 5, 页码 -

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CELL PRESS
DOI: 10.1016/j.cub.2020.12.045

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资金

  1. National Science Foundation (NSF) AToL grant [DEB0622764]
  2. NSF [DEB1120243]
  3. Harvard University

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Despite significant differences in genome size among angiosperms, key features of genome architecture are largely conserved. The highly modified genome of Sapria himalayana Griff. demonstrates high levels of gene loss compared to other vascular plants and extreme disparity in intron size among retained genes. Furthermore, at least 1.2% of the Sapria genome is inferred to be derived from host-to-parasite horizontal gene transfers, highlighting the value of HGTs as DNA fossils to study extinct symbioses.
Despite more than 2,000-fold variation in genome size, key features of genome architecture are largely conserved across angiosperms. Parasitic plants have elucidated the many ways in which genomes can be modified, yet we still lack comprehensive genome data for species that represent the most extreme form of parasitism. Here, we present the highly modified genome of the iconic endophytic parasite Sapria himalayana Griff. (Rafflesiaceae), which lacks a typical plant body. First, 44% of the genes conserved in eurosids are lost in Sapria, dwarfing previously reported levels of gene loss in vascular plants. These losses demonstrate remarkable functional convergence with other parasitic plants, suggesting a common genetic road map underlying the evolution of plant parasitism. Second, we identified extreme disparity in intron size among retained genes. This includes a category of genes with introns longer than any so far observed in angiosperms, nearing 100 kb in some cases, and a second category of genes with exceptionally short or absent introns. Finally, at least 1.2% of the Sapria genome, including both genic and intergenic content, is inferred to be derived from host-to-parasite horizontal gene transfers (HGTs) and includes genes potentially adaptive for parasitism. Focused phylogenomic reconstruction of HGTs reveals a hidden history of former host-parasite associations involving close relatives of Sapria's modern hosts in the grapevine family. Our findings offer a unique perspective into how deeply angiosperm genomes can be altered to fit an extreme form of plant parasitism and demonstrate the value of HGTs as DNA fossils to investigate extinct symbioses.

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