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 - Publisher Copyright:
Copyright © 2025 the Author(s).
PY - 2025/4/22
Y1 - 2025/4/22
N2 - 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 (V g) underwent five independent loss events in four families, involving 23 of the analyzed endoparasitoid species. Whole-genome alignment suggested that V g loss occurred during genome rearrangement events. Analysis of V g receptor gene (V gR) loss, selection, and structural variation in lineages lacking V g demonstrated functional biases in the patterns of gene loss. The ectoparasitism to endoparasitism transition did not appear to be the primary driver of V g loss or the subsequent V gR 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 - 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 (V g) underwent five independent loss events in four families, involving 23 of the analyzed endoparasitoid species. Whole-genome alignment suggested that V g loss occurred during genome rearrangement events. Analysis of V g receptor gene (V gR) loss, selection, and structural variation in lineages lacking V g demonstrated functional biases in the patterns of gene loss. The ectoparasitism to endoparasitism transition did not appear to be the primary driver of V g loss or the subsequent V gR 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.
KW - gene loss
KW - parasitoid
KW - vitellogenin
KW - vitellogenin receptor
KW - yolk protein loss
UR - https://www.scopus.com/pages/publications/105003443083
U2 - 10.1073/pnas.2422292122
DO - 10.1073/pnas.2422292122
M3 - Article
C2 - 40232796
SN - 0027-8424
VL - 122
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 16
M1 - e2422292122
ER -