Feeding‐structure morphogenesis in “rhabditid” and diplogastrid nematodes is not controlled by a conserved genetic module

Abstract

Disentangling the evolution of the molecular processes and genetic networks that facilitate the emergence of morphological novelties is one of the main objectives in evolutionary developmental biology. Here, we investigated the evolutionary history of a gene regulatory network controlling the development of novel tooth‐like feeding structures in diplogastrid nematodes. Focusing on NHR‐1 and NHR‐40, the two transcription factors that regulate the morphogenesis of these feeding structures in Pristionchus pacificus, we sought to determine whether they have a similar function in Caenorhabditis elegans, an outgroup species to the Diplogastridae which has typical “rhabditid” flaps instead of teeth. Contrary to our initial expectations, we found that they do not have a similar function. While both receptors are co‐expressed in the tissues that produce the feeding structures in the two nematodes, genetic inactivation of either receptor had no impact on feeding‐structure morphogenesis in C. elegans. Transcriptomic experiments revealed that NHR‐1 and NHR‐40 have highly species‐specific regulatory targets. These results suggest two possible evolutionary scenarios: either the genetic module responsible for feeding‐structure morphogenesis in Diplogastridae already existed in the last common ancestor of C. elegans and P. pacificus, and subsequently disintegrated in the former as NHR‐1 and NHR‐40 acquired new targets, or it evolved in conjunction with teeth in Diplogastridae. These findings indicate that feeding‐structure morphogenesis is regulated by different genetic programs in P. pacificus and C. elegans, hinting at developmental systems drift during the flap‐to‐tooth transformation. Further research in other “rhabditid” species is needed to fully reconstruct the developmental genetic changes which facilitated the evolution of novel feeding structures in Diplogastridae.