Nutritional specialization and social evolution in woodroaches and termites

Woodroach biparental-care and termite sibling-altruism evolved from solitary cockroach ancestors following nutritional specialization on nutrient-deficient dead-wood, but the accompanying genomic changes remained unclear. We sequenced eight new Blattodea species showing stepwise contracted genomes. Woodroach brood-rearing remained constrained by deactivated oxidative phosphorylation and peroxisome genes, consistent with slow immature growth. Termites lost key genes mediating sperm motility, corroborating that reproductive division of labor required monogamous colony-founding. They also co-opted many genes from fundamental nutrition-sensitive juvenile hormone, insulin, EGFR and Dpp signaling pathways. Thus, most larvae develop as workers via high energy metabolism early on, while reproductive nymphs highly express energy metabolism genes late in development. These pathways are consistent with obligate dependence on provisioning by specialized workers and feedback loops allowing large homeostatic colonies to evolve.

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Publication Details

Journal
Science
Published
2026-01-29
DOI
https://doi.org/10.1126/science.adt2178
Citations
1
Primary Topic
Insect and Arachnid Ecology and Behavior
Type
article
Field-Weighted Citation Impact
30.93
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article

Nutritional specialization and social evolution in woodroaches and termites

Yun‐Xia Luan, Qian Gao, F. H. Liu, Kesen Zhu et al.
1 citations
Science
Insect and Arachnid Ecology and Behavior
30.93
article

Nutritional specialization and social evolution in woodroaches and termites

Yun‐Xia Luan, Qian Gao, F. H. Liu, Kesen Zhu, Shuxin Yu, Nathan C. Lo, Qiuying Huang, Shiming Zhu, Zhaoxin Li, Hui Xiang, Mingtao Liao, Zhang Wang, YINGYING CUI, Zongqing Wang, Melissa Sánchez Herrera, Xiaohong Su, Jacobus J. Boomsma, Gangqi Fang, Shuai Wang, Jinlan Xu, Dongwei Yuan, Sheng Li, Yunlong Cheng
article en
1 citations

Abstract

Woodroach biparental-care and termite sibling-altruism evolved from solitary cockroach ancestors following nutritional specialization on nutrient-deficient dead-wood, but the accompanying genomic changes remained unclear. We sequenced eight new Blattodea species showing stepwise contracted genomes. Woodroach brood-rearing remained constrained by deactivated oxidative phosphorylation and peroxisome genes, consistent with slow immature growth. Termites lost key genes mediating sperm motility, corroborating that reproductive division of labor required monogamous colony-founding. They also co-opted many genes from fundamental nutrition-sensitive juvenile hormone, insulin, EGFR and Dpp signaling pathways. Thus, most larvae develop as workers via high energy metabolism early on, while reproductive nymphs highly express energy metabolism genes late in development. These pathways are consistent with obligate dependence on provisioning by specialized workers and feedback loops allowing large homeostatic colonies to evolve.

Science
University of Copenhagen (DK), The University of Sydney (AU), American Museum of Natural History (US), Southwest University (CN), Universidad de Los Andes (CO), China West Normal University (CN), University of Alabama (US), South China Normal University (CN), Chinese Academy of Sciences (CN), Huazhong Agricultural University (CN), Northwest University (CN), Center for Excellence in Molecular Plant Sciences (CN), Universidad de Los Andes (BO)
Zero hunger
Openalex Percentile: Top 1%
Insect and Arachnid Ecology and Behavior
30.93
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