TY - JOUR
T1 - Evidence for miRNA-mediated modulation of the host transcriptome in cnidarian-dinoflagellate symbiosis
AU - Baumgarten, Sebastian
AU - Cziesielski, Maha Joana
AU - Thomas, Ludivine
AU - Michell, Craig
AU - Esherick, Lisl Y.
AU - Pringle, John R.
AU - Aranda, Manuel
AU - Voolstra, Christian R.
N1 - KAUST Repository Item: Exported on 2020-10-01
Acknowledgements: Research reported in this publication was supported by the King Abdullah University of Science and Technology (KAUST) and by Gordon and Betty Moore Foundation Grant 2629.01 (to J.R.P.). We thank the Bioscience Core lab and the Imaging and Characterization Core lab at KAUST for help with the protein characterization and microscopy. Figure 5 was created by Heno Hwang, scientific illustrator at KAUST.
PY - 2017/12/23
Y1 - 2017/12/23
N2 - Reef-building corals and other cnidarians living in symbiotic relationships with intracellular, photosynthetic dinoflagellates in the genus Symbiodinium undergo transcriptomic changes during infection with the algae and maintenance of the endosymbiont population. However, the precise regulatory mechanisms modulating the host transcriptome are unknown. Here we report apparent post-transcriptional gene regulation by miRNAs in the sea anemone Aiptasia, a model system for cnidarian-dinoflagellate endosymbiosis. Aiptasia encodes mainly species-specific miRNAs, and there appears to have been recent differentiation within the Aiptasia genome of miRNAs that are commonly conserved among anthozoan cnidarians. Analysis of miRNA expression showed that both conserved and species-specific miRNAs are differentially expressed in response to endosymbiont infection. Using cross-linking immunoprecipitation of Argonaute, the central protein of the miRNA-induced silencing complex, we identified miRNA binding sites on a transcriptome-wide scale and found that the targets of the miRNAs regulated in response to symbiosis include genes previously implicated in biological processes related to Symbiodinium infection. Our study shows that cnidarian miRNAs recognize their mRNA targets via high-complementarity target binding and suggests that miRNA-mediated modulations of genes and pathways are important during the onset and maintenance of cnidarian-dinoflagellate endosymbiosis. This article is protected by copyright. All rights reserved.
AB - Reef-building corals and other cnidarians living in symbiotic relationships with intracellular, photosynthetic dinoflagellates in the genus Symbiodinium undergo transcriptomic changes during infection with the algae and maintenance of the endosymbiont population. However, the precise regulatory mechanisms modulating the host transcriptome are unknown. Here we report apparent post-transcriptional gene regulation by miRNAs in the sea anemone Aiptasia, a model system for cnidarian-dinoflagellate endosymbiosis. Aiptasia encodes mainly species-specific miRNAs, and there appears to have been recent differentiation within the Aiptasia genome of miRNAs that are commonly conserved among anthozoan cnidarians. Analysis of miRNA expression showed that both conserved and species-specific miRNAs are differentially expressed in response to endosymbiont infection. Using cross-linking immunoprecipitation of Argonaute, the central protein of the miRNA-induced silencing complex, we identified miRNA binding sites on a transcriptome-wide scale and found that the targets of the miRNAs regulated in response to symbiosis include genes previously implicated in biological processes related to Symbiodinium infection. Our study shows that cnidarian miRNAs recognize their mRNA targets via high-complementarity target binding and suggests that miRNA-mediated modulations of genes and pathways are important during the onset and maintenance of cnidarian-dinoflagellate endosymbiosis. This article is protected by copyright. All rights reserved.
UR - http://hdl.handle.net/10754/626371
UR - http://onlinelibrary.wiley.com/doi/10.1111/mec.14452/abstract
UR - http://www.scopus.com/inward/record.url?scp=85039546435&partnerID=8YFLogxK
U2 - 10.1111/mec.14452
DO - 10.1111/mec.14452
M3 - Article
C2 - 29218749
SN - 0962-1083
VL - 27
SP - 403
EP - 418
JO - Molecular Ecology
JF - Molecular Ecology
IS - 2
ER -