Genomic signatures associated with the evolutionary loss of egg yolk in parasitoid wasps

Xianxin Zhao, Yuanyuan Liu, Bo Yuan, Zhichao Cao, Yi Yang, Chun He, Kevin C. Chan, Shan Xiao, Haiwei Lin, Qi Fang, Gongyin Ye*, Xinhai Ye*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

Parasitoid wasps have evolved yolkless eggs in many species. However, the genomic changes underlying this trait loss remain poorly understood. Comparative genomic analysis of 64 hymenopteran insects shows five independent loss events of the yolk protein gene vitellogenin (Vg) in 23 endoparasitoid species across four families. These losses are likely linked to genomic rearrangements and loss or relaxed selection of vitellogenin receptor (VgR), suggesting coordinated gene function elimination. We suggest that the transition from ectoparasitism (embryonic development outside the host) to endoparasitism (development within the host hemolymph) reduced selective pressure on yolk-related functions. This work offers insights into the genomic changes underlying trait loss and emphasizes how ecological adaptation can shape genome architecture in parasitoids. Trait regression and loss have occurred repeatedly in numerous lineages in response to environmental changes. In parasitoid wasps, a megadiverse group of hymenopteran insects, yolk protein reduction or loss has been observed in many species, likely linked to the transition from ectoparasitism to endoparasitism. However, the genetic basis of this trait and the impact of its loss on genome evolution remain poorly understood. Here, we performed a comparative genomic analysis of 64 hymenopteran insects. The conserved insect yolk protein gene vitellogenin (Vg) underwent five independent loss events in four families, involving 23 of the analyzed endoparasitoid species. Whole-genome alignment suggested that Vg loss occurred during genome rearrangement events. Analysis of Vg receptor gene (VgR) loss, selection, and structural variation in lineages lacking Vg demonstrated functional biases in the patterns of gene loss. The ectoparasitism to endoparasitism transition did not appear to be the primary driver of Vg loss or the subsequent VgR evolution. Together, these findings reveal the genomic changes underlying a unique trait loss in parasitoid wasps. More broadly, this study enhances our understanding of yolk protein loss evolution outside the class Mammalia, highlighting a potential evolutionary trend arising from the availability of an alternative nutrient source for embryonic development.
Original languageEnglish
Pages (from-to)e2422292122
JournalProceedings of the National Academy of Sciences
Volume122
Issue number16
DOIs
Publication statusPublished - May 2025

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