Literature DB >> 34521754

Emergent RNA-RNA interactions can promote stability in a facultative phototrophic endosymbiosis.

Benjamin H Jenkins1,2, Finlay Maguire3, Guy Leonard4,2, Joshua D Eaton4, Steven West4, Benjamin E Housden5, David S Milner4,2, Thomas A Richards1,2.   

Abstract

Eukaryote-eukaryote endosymbiosis was responsible for the spread of chloroplast (plastid) organelles. Stability is required for the metabolic and genetic integration that drives the establishment of new organelles, yet the mechanisms that act to stabilize emergent endosymbioses-between two fundamentally selfish biological organisms-are unclear. Theory suggests that enforcement mechanisms, which punish misbehavior, may act to stabilize such interactions by resolving conflict. However, how such mechanisms can emerge in a facultative endosymbiosis has yet to be explored. Here, we propose that endosymbiont-host RNA-RNA interactions, arising from digestion of the endosymbiont population, can result in a cost to host growth for breakdown of the endosymbiosis. Using the model facultative endosymbiosis between Paramecium bursaria and Chlorella spp., we demonstrate that this mechanism is dependent on the host RNA-interference (RNAi) system. We reveal through small RNA (sRNA) sequencing that endosymbiont-derived messenger RNA (mRNA) released upon endosymbiont digestion can be processed by the host RNAi system into 23-nt sRNA. We predict multiple regions of shared sequence identity between endosymbiont and host mRNA, and demonstrate through delivery of synthetic endosymbiont sRNA that exposure to these regions can knock down expression of complementary host genes, resulting in a cost to host growth. This process of host gene knockdown in response to endosymbiont-derived RNA processing by host RNAi factors, which we term "RNAi collisions," represents a mechanism that can promote stability in a facultative eukaryote-eukaryote endosymbiosis. Specifically, by imposing a cost for breakdown of the endosymbiosis, endosymbiont-host RNA-RNA interactions may drive maintenance of the symbiosis across fluctuating ecological conditions.
Copyright © 2021 the Author(s). Published by PNAS.

Entities:  

Keywords:  algae; cell–cell interaction; coevolution; protist; symbiosis

Mesh:

Substances:

Year:  2021        PMID: 34521754      PMCID: PMC8463893          DOI: 10.1073/pnas.2108874118

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   12.779


  66 in total

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9.  Characterization of the RNA-interference pathway as a tool for reverse genetic analysis in the nascent phototrophic endosymbiosis, Paramecium bursaria.

Authors:  Benjamin H Jenkins; Finlay Maguire; Guy Leonard; Joshua D Eaton; Steven West; Benjamin E Housden; David S Milner; Thomas A Richards
Journal:  R Soc Open Sci       Date:  2021-04-21       Impact factor: 2.963

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2.  Emergent RNA-RNA interactions can promote stability in a facultative phototrophic endosymbiosis.

Authors:  Benjamin H Jenkins; Finlay Maguire; Guy Leonard; Joshua D Eaton; Steven West; Benjamin E Housden; David S Milner; Thomas A Richards
Journal:  Proc Natl Acad Sci U S A       Date:  2021-09-21       Impact factor: 12.779

3.  Establishment of Host-Algal Endosymbioses: Genetic Response to Symbiont Versus Prey in a Sponge Host.

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Journal:  Genome Biol Evol       Date:  2021-11-05       Impact factor: 3.416

  3 in total

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