bioRxivGenomicsPreprint
The hologenome of Osedax frankpressi reveals the genetic interplay for the symbiotic digestion of vertebrate bone
Giacomo Moggioli, Balig PanossianiD, Yanan SuniD, Daniel J. ThieliD, Francisco M. Martín-ZamoraiD, Martin Tran, Alexander Michael CliffordiD, Shana K. GoffrediiD, N. N. Rimskaya-KorsakovaiD, Gáspár JékelyiD, Martín TresguerresiD, Pei‐Yuan QianiD, Jian‐Wen QiuiD, Greg W. RouseiD, Lee M. HenryiD, José María Martín-DurániD
Abstract
The marine annelid Osedax has evolved a unique heterotrophic symbiosis that allows it to feed exclusively on sunken bones. Yet, the genetic and physiological principles sustaining this symbiosis are poorly understood. Here we show that Osedax frankpressi has a small, AT-rich genome shaped by extensive gene loss. While the Oceanospirillales endosymbiont of Osedax is enriched in genes for carbohydrate and nitrogen metabolism, O. frankpressi has undergone genetic changes to accommodate bone digestion, including the expansion of matrix metalloproteases, and a loss of pathways to synthesize amino acids that are abundant in collagen. Unlike other symbioses, however, innate immunity genes required to acquire and control the endosymbionts are reduced in O. frankpressi. These findings reveal Osedax has evolved an alternative genomic toolkit to bacterial symbiosis where host-symbiont co-dependence has favoured genome simplicity in the host to exploit the nutritionally unbalanced diet of bones. TeaserGenome reduction and adaptations for collagen digestion underpin the symbiosis of Osedax worms to exploit decaying bones.
- assay: whole-genome sequencing
- research focus: gene regulatory network inference
- research focus: differential expression
- research focus: variant calling
- approach: statistical model
- Citations
- 1
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