Comparing the potential for maternal-fetal signalling in oviparous and viviparous lizards.

Philos Trans R Soc Lond B Biol Sci

School of BioSciences, University of Melbourne, Victoria 3052, Australia.

Published: December 2022

AI Article Synopsis

  • The evolution of placenta involves changing reproductive timing, enhancing nutrient exchange, and improving communication between mother and fetus.
  • A study on gene expression in live-bearing and egg-laying lizards found around 70% of ligand/receptor genes are shared, but only the live-bearing species showed enrichment in specific signaling pathways related to fetal control of placentation.
  • Notably, the signaling molecule inhibin beta B (INHBB) appeared in the fetal membranes of live-bearing lizards but was absent in egg-laying relatives, indicating significant evolutionary changes in maternal-fetal signaling for viviparity.

Article Abstract

The evolution of a placenta requires several steps including changing the timing of reproductive events, facilitating nutrient exchange, and the capacity for maternal-fetal communication. To understand the evolution of maternal-fetal communication, we used ligand-receptor gene expression as a proxy for the potential for cross-talk in a live-bearing lizard () and homologous tissues in a related egg-laying lizard (). Approximately 70% of expressed ligand/receptor genes were shared by both species. Gene ontology (GO) analysis showed that there was no GO-enrichment in the fetal membranes of the egg-laying species, but live-bearing fetal tissues were significantly enriched for 50 GO-terms. Differences in enrichment suggest that the evolution of viviparity involved reinforcing specific signalling pathways, perhaps to support fetal control of placentation. One identified change was in transforming growth factor beta signalling. Using immunohistochemistry, we show the production of the signalling molecule inhibin beta B (INHBB) occurs in viviparous fetal membranes but was absent in closely related egg-laying tissues, suggesting that the evolution of viviparity may have involved changes to signalling via this pathway. We argue that maternal-fetal signalling evolved through co-opting expressed signalling molecules and recruiting new signalling molecules to support the complex developmental changes required to support a fetus . This article is part of the theme issue 'Extraembryonic tissues: exploring concepts, definitions and functions across the animal kingdom'.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9574625PMC
http://dx.doi.org/10.1098/rstb.2021.0262DOI Listing

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