4.4 Article

Retinoids promote penis development in sequentially hermaphroditic snails

Journal

DEVELOPMENTAL BIOLOGY
Volume 478, Issue -, Pages 122-132

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ydbio.2021.06.013

Keywords

Crepidula; Imposex; Tributyltin; Genital development; Environmental sex determination

Funding

  1. National Science Foundation [NSF IOS-1558061, NSF EDGE IOS-1827533]
  2. Fonds de recherche quebecois -Nature et Technologie
  3. Society for Developmental Biology
  4. Whitman Early Career Research Fellowships at the Marine Biological Laboratory (Woods Hole, MA, USA)

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Sexual systems display diversity despite the prevalence of sexual reproduction, with sequential hermaphroditism emerging independently multiple times across the animal kingdom. In molluscs, shifts between ancestral separate sexes and hermaphroditism occur at the family level, suggesting recruitment of deeply conserved mechanisms. The role of retinoid signaling in molluscan male development and shifts in timing may have been important for the origins of sequential hermaphroditism within molluscs.
Sexual systems are surprisingly diverse, considering the ubiquity of sexual reproduction. Sequential hermaphroditism, the ability of an individual to change sex, has emerged multiple times independently across the animal kingdom. In molluscs, repeated shifts between ancestrally separate sexes and hermaphroditism are generally found at the level of family and above, suggesting recruitment of deeply conserved mechanisms. Despite this, molecular mechanisms of sexual development are poorly known. In molluscs with separate sexes, endocrine disrupting toxins bind the retinoid X receptor (RXR), activating ectopic male development in females, suggesting the retinoid pathway as a candidate controlling sexual transitions in sequential hermaphrodites. We therefore tested the role of retinoic acid signaling in sequentially hermaphroditic Crepidula snails, which develop first into males, then change sex, maturing into females. We show that retinoid agonists induce precocious penis growth in juveniles and superimposition of male development in females. Combining RXR antagonists with retinoid agonists significantly reduces penis length in induced juveniles, while similar treatments using retinoic acid receptor (RAR) antagonists increase penis length. Transcripts of both receptors are expressed in the induced penis. Our findings therefore show that retinoid signaling can initiate molluscan male genital development, and regulate penis length. Further, we show that retinoids induce ectopic male development in multiple Crepidula species. Species-specific influence of conspecific induction of sexual transitions correlates with responsiveness to retinoids. We propose that retinoid signaling plays a conserved role in molluscan male development, and that shifts in the timing of retinoid signaling may have been important for the origins of sequential hermaphroditism within molluscs.

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