TY - UNPB
T1 - Sequential evolution of antidote and toxin links genetic incompatibility with immune responses
AU - Xie, Dongying
AU - Ma, Yiming
AU - Zeng, Junhui
AU - Ye, Pohao
AU - Zhao, Zhongying
N1 - This work was supported by General Research Funds from the Hong Kong Research Grants Council (HKBU12100825, HKBU12101522, HKBU12101323, HKBU12100024), the Hong Kong Innovation and Technology Fund (GHP/176/21SZ), the Environment and Conservation Fund (2023-160) from the Hong Kong Environmental Protection Department, and Seed Funding for Collaborative Research Grants (RC-SFCRG/24-25/R1/SCI/01) from Hong Kong Baptist University to Z.Z. The work was also supported by the Young Scientists Fund from National Natural Science Foundation of China (32400491), and the General Research Fund from the Hong Kong Research Grants Council (HKBU12100925) to X.D. This study was supported by the Wu Jieh Yee Institute of Translational Chinese Medicine Research, Hong Kong Baptist University.
PY - 2026/1/8
Y1 - 2026/1/8
N2 - Toxin-antidote (TA) systems are selfish genetic elements that promote their own inheritance by selectively eliminating offspring lacking the module, thereby establishing post-zygotic genetic incompatibilities between individuals and populations. Although these systems are widespread across species, their evolutionary origins remain poorly understood. Here, we report the discovery of a novel TA gene pair in the nematode Caenorhabditis nigoni. The antidote gene, Cni-shls-2, is a species-specific F-box gene that arose through recent tandem duplications. Its absence results in embryonic lethality in both C. nigoni and its hybrids with the sister species C. briggsae. This lethality is caused by a maternally deposited toxin, Cni-hlix-1, a chimeric gene formed through the fusion of host and bacterial sequences. Phylogenetic and genomic analyses reveal a sequential evolution of the TA system, in which the antidote evolved prior to the toxin. The stepwise evolution of TA and the potential microbial origin of the toxin support the hypothesis that the antidote initially evolved in response to pathogen exposure, followed by the domestication of the toxin, thereby elucidating the origins of TA formation. These findings highlight the central role of host-pathogen conflict as a driving force in the emergence of genetic incompatibilities and the evolution of reproductive barriers.
AB - Toxin-antidote (TA) systems are selfish genetic elements that promote their own inheritance by selectively eliminating offspring lacking the module, thereby establishing post-zygotic genetic incompatibilities between individuals and populations. Although these systems are widespread across species, their evolutionary origins remain poorly understood. Here, we report the discovery of a novel TA gene pair in the nematode Caenorhabditis nigoni. The antidote gene, Cni-shls-2, is a species-specific F-box gene that arose through recent tandem duplications. Its absence results in embryonic lethality in both C. nigoni and its hybrids with the sister species C. briggsae. This lethality is caused by a maternally deposited toxin, Cni-hlix-1, a chimeric gene formed through the fusion of host and bacterial sequences. Phylogenetic and genomic analyses reveal a sequential evolution of the TA system, in which the antidote evolved prior to the toxin. The stepwise evolution of TA and the potential microbial origin of the toxin support the hypothesis that the antidote initially evolved in response to pathogen exposure, followed by the domestication of the toxin, thereby elucidating the origins of TA formation. These findings highlight the central role of host-pathogen conflict as a driving force in the emergence of genetic incompatibilities and the evolution of reproductive barriers.
UR - https://www.biorxiv.org/content/10.64898/2026.01.07.698274v1
U2 - 10.64898/2026.01.07.698274
DO - 10.64898/2026.01.07.698274
M3 - Preprint
T3 - bioRxiv
BT - Sequential evolution of antidote and toxin links genetic incompatibility with immune responses
PB - Cold Spring Harbor Laboratory
ER -