TY - JOUR
T1 - Genomic signatures associated with the evolutionary loss of egg yolk in parasitoid wasps
AU - Zhao, Xianxin
AU - Liu, Yuanyuan
AU - Yuan, Bo
AU - Cao, Zhichao
AU - Yang, Yi
AU - He, Chun
AU - Chan, Kevin C.
AU - Xiao, Shan
AU - Lin, Haiwei
AU - Fang, Qi
AU - Ye, Gongyin
AU - Ye, Xinhai
N1 - doi: 10.1073/pnas.2422292122
PY - 2025/5
Y1 - 2025/5
N2 - 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.
AB - 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.
U2 - 10.1073/pnas.2422292122
DO - 10.1073/pnas.2422292122
M3 - Article
VL - 122
SP - e2422292122
JO - Proceedings of the National Academy of Sciences
JF - Proceedings of the National Academy of Sciences
IS - 16
ER -