Evidence map›Paper›PMID 41275382›Full record

ArticleMolecular biology and evolution2025

Ancestral Sequence Reconstruction Provides Insights into the Structural Diversification and Neofunctionalization of T-superfamily Conotoxins in Conus.

Samuel S Espino, Thomas Lund Koch, Joanna Gajewiak, Matías L Giglio, Maren Watkins, Helena Safavi-Hemami, Baldomero M Olivera

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Article in Molecular biology and evolution, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Samuel S EspinoSchool of Biological Sciences, University of Utah, 257 S 1400 E, Salt Lake City, UT 84112, USA.ORCID 0009-0000-8917-1057
Thomas Lund KochSchool of Biological Sciences, University of Utah, 257 S 1400 E, Salt Lake City, UT 84112, USA.ORCID 0000-0002-8489-0375
Joanna GajewiakSchool of Biological Sciences, University of Utah, 257 S 1400 E, Salt Lake City, UT 84112, USA.ORCID 0000-0003-3608-9935
Matías L GiglioSchool of Biological Sciences, University of Utah, 257 S 1400 E, Salt Lake City, UT 84112, USA.ORCID 0000-0002-6357-9772
Maren WatkinsSchool of Biological Sciences, University of Utah, 257 S 1400 E, Salt Lake City, UT 84112, USA.ORCID 0000-0002-4127-1961
Helena Safavi-HemamiSchool of Biological Sciences, University of Utah, 257 S 1400 E, Salt Lake City, UT 84112, USA.ORCID 0000-0002-1984-2721
Baldomero M OliveraSchool of Biological Sciences, University of Utah, 257 S 1400 E, Salt Lake City, UT 84112, USA.ORCID 0000-0003-4556-1410

Funding

“Conus venom peptides and their molecular targets: Using pharmaconomics and neuroethology as a framework for discovery”R01GM144719 · NIGMS · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI OLIVERA, BALDOMERO M, RAGHURAMAN, SHRINIVASAN · 2022 to 2025
$2.5M
Independent Research Fund Denmark 3102-00006BNIGMS NIH HHS R01 GM144719NIGMS NIH HHS R01GM144719
6 · The paper itself

Abstract

Due to their remarkable diversity and rapid evolution, conotoxins-peptide toxins from predatory marine cone snails-provide a powerful system for exploring how gene diversification may contribute to the development of lineage-specific adaptations. We previously demonstrated that 2-loop Tau conotoxins represent an evolutionary innovation associated with mollusk-hunting behaviors in cone snails. Here, we investigate the evolutionary history of these toxins as a model to understand the mechanism of ancestral gene neofunctionalization, which may have contributed to the emergence of mollusk-hunting in cone snails. Using ancestral sequence reconstruction, we present a model in which ancestral T-superfamily conotoxins neofunctionalized into the 2-loop Tau conotoxins. Predicted ancestral sequences reveal an intermediate structure between the classic T-superfamily conotoxins and the derived 2-loop Tau forms. Notably, these ancestral intermediates acquired a new cysteine scaffold that facilitated a structural transition from a globular to a ribbon fold. This conformational shift was followed by sequence-level changes that presumably enhanced activity against molecular targets in mollusks. We propose that the emergence of 2-loop Tau conotoxins may have been one factor that contributed to the emergence of molluscivory, providing insight into how gene innovation may underlie ecological diversification.

Indexed as

ConotoxinsConus SnailAmino Acid SequenceAnimalsEvolution, MolecularPhylogenyConotoxinsancestral sequence reconstructionCone snailconotoxingene neofunctionalizationlineage specific adaptationstructural diversification

Identifiers

PMID41275382
PMCPMC12686989

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