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Micro and macroevolution of sea anemone venom phenotype

Author

Listed:
  • Edward G. Smith

    (University of North Carolina at Charlotte, Department of Biological Sciences
    University of Warwick)

  • Joachim M. Surm

    (The Hebrew University of Jerusalem)

  • Jason Macrander

    (University of North Carolina at Charlotte, Department of Biological Sciences
    Florida Southern College, Biology Department)

  • Adi Simhi

    (The Hebrew University of Jerusalem
    The Hebrew University of Jerusalem, The School of Computer Science & Engineering)

  • Guy Amir

    (The Hebrew University of Jerusalem
    The Hebrew University of Jerusalem, The School of Computer Science & Engineering)

  • Maria Y. Sachkova

    (The Hebrew University of Jerusalem
    University of Bergen)

  • Magda Lewandowska

    (The Hebrew University of Jerusalem)

  • Adam M. Reitzel

    (University of North Carolina at Charlotte, Department of Biological Sciences)

  • Yehu Moran

    (The Hebrew University of Jerusalem)

Abstract

Venom is a complex trait with substantial inter- and intraspecific variability resulting from strong selective pressures acting on the expression of many toxic proteins. However, understanding the processes underlying toxin expression dynamics that determine the venom phenotype remains unresolved. By interspecific comparisons we reveal that toxin expression in sea anemones evolves rapidly and that in each species different toxin family dictates the venom phenotype by massive gene duplication events. In-depth analysis of the sea anemone, Nematostella vectensis, revealed striking variation of the dominant toxin (Nv1) diploid copy number across populations (1-24 copies) resulting from independent expansion/contraction events, which generate distinct haplotypes. Nv1 copy number correlates with expression at both the transcript and protein levels with one population having a near-complete loss of Nv1 production. Finally, we establish the dominant toxin hypothesis which incorporates observations in other venomous lineages that animals have convergently evolved a similar strategy in shaping their venom.

Suggested Citation

  • Edward G. Smith & Joachim M. Surm & Jason Macrander & Adi Simhi & Guy Amir & Maria Y. Sachkova & Magda Lewandowska & Adam M. Reitzel & Yehu Moran, 2023. "Micro and macroevolution of sea anemone venom phenotype," Nature Communications, Nature, vol. 14(1), pages 1-17, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-35794-9
    DOI: 10.1038/s41467-023-35794-9
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    1. Kristian W. Sanggaard & Jesper S. Bechsgaard & Xiaodong Fang & Jinjie Duan & Thomas F. Dyrlund & Vikas Gupta & Xuanting Jiang & Ling Cheng & Dingding Fan & Yue Feng & Lijuan Han & Zhiyong Huang & Zong, 2014. "Spider genomes provide insight into composition and evolution of venom and silk," Nature Communications, Nature, vol. 5(1), pages 1-12, September.
    2. Zhijian Cao & Yao Yu & Yingliang Wu & Pei Hao & Zhiyong Di & Yawen He & Zongyun Chen & Weishan Yang & Zhiyong Shen & Xiaohua He & Jia Sheng & Xiaobo Xu & Bohu Pan & Jing Feng & Xiaojuan Yang & Wei Hon, 2013. "The genome of Mesobuthus martensii reveals a unique adaptation model of arthropods," Nature Communications, Nature, vol. 4(1), pages 1-10, December.
    3. Kristian W. Sanggaard & Jesper S. Bechsgaard & Xiaodong Fang & Jinjie Duan & Thomas F. Dyrlund & Vikas Gupta & Xuanting Jiang & Ling Cheng & Dingding Fan & Yue Feng & Lijuan Han & Zhiyong Huang & Zong, 2014. "Correction: Corrigendum: Spider genomes provide insight into composition and evolution of venom and silk," Nature Communications, Nature, vol. 5(1), pages 1-1, December.
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