Symbiosis-driven development in an early branching metazoan
Aki H. OhderaiD, Justin Darymple, Viridiana Avila‐MagañaiD, Victoria J. A. SharpiD, Kelly E. WatsoniD, Mark McCauleyiD, Bailey M. SteinworthiD, Erika M Diaz-AlmeydaiD, Sheila A. KitcheniD, Angela Z. PooleiD, Anthony Bellantuono, Sajeet HaridasiD, Igor V. GrigorieviD, Lea A. GoentoroiD, Elizabeth A. Vallen, David Michael BakeriD, Todd C. LaJeunesseiD, Sandra LoesgeniD, Mark Q. MartindaleiD, Matthew DeGennaroiD, William K. FittiD, Mónica MedinaiD
Abstract
Microbes can initiate developmental gene regulatory cascades in animals. The molecular mechanisms underlying microbe-induced animal development and the evolutionary steps to integrate microbial signals into regulatory programs remain poorly understood. In the upside-down jellyfish Cassiopea xamachana, a dinoflagellate endosymbiont initiates the life stage transition from the sessile polyp to the sexual medusa. We found that metabolic products derived from symbiont carotenoids may be important to initiate C. xamachana development, in addition to expression of conserved genes involved in medusa development of non-symbiotic jellyfish. We also revealed the transcription factor COUP is expressed during metamorphosis, potentially as a co-regulator of nuclear receptor RXR. These data suggest relatively few steps may be necessary to integrate symbiont signals into gene regulatory networks and cements the role of the symbiont as a key trigger for life history transition in C. xamachana.
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