Evidence map›Paper›PMID 41466268›Full record

ArticleBMC biology2025

Molecular mechanisms underlying early functional divergence in snake venom inferred from the genomes of two pitviper lineages.

Andrew J Mason, Pedro G Nachtigall, Darin R Rokyta, Christopher L Parkinson, Felipe G Grazziotin, Inácio L M Junqueira-de-Azevedo, H Lisle Gibbs

Abstract read
In one paragraph

Article in BMC biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. The genomic origins and evolutionary path to a key innovation in the world's most venomous snakes.Proceedings of the National Academy of Sciences of the United States of America · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Andrew J MasonDepartment of Evolution, Ecology, and Organismal Biology, The Ohio State University, Columbus, OH, 43210, USA. mason.501@osu.edu.ORCID 0000-0003-0297-1313
Pedro G NachtigallLaboratório de Toxinologia Aplicada, Center of Toxins, Immune-Response and Cell Signaling (CeTICS), Instituto Butantan, São Paulo, SP, 05503-900, Brazil. pedronachtigall@gmail.com.
Darin R RokytaDepartment of Biological Science, Florida State University, Tallahassee, FL, 32306, USA.
Christopher L ParkinsonDepartment of Biological Sciences, Clemson University, Clemson, SC, 29634, USA.
Felipe G GrazziotinLaboratório de Coleções Zoológicas, Instituto Butantan, São Paulo, SP, 05503-900, Brazil.
Inácio L M Junqueira-de-AzevedoLaboratório de Toxinologia Aplicada, Center of Toxins, Immune-Response and Cell Signaling (CeTICS), Instituto Butantan, São Paulo, SP, 05503-900, Brazil. inacio.azevedo@butantan.gov.br.
H Lisle GibbsDepartment of Evolution, Ecology, and Organismal Biology, The Ohio State University, Columbus, OH, 43210, USA. gibbs.128@osu.edu.

Funding

Division of Environmental Biology 1638872Division of Environmental Biology 1638879Division of Environmental Biology 1638902Division of Environmental Biology 822417Fundação de Amparo à Pesquisa do Estado de São Paulo 2016/50127-5Fundação de Amparo à Pesquisa do Estado de São Paulo 2018/26520-
6 · The paper itself

Abstract

backgroundThe molecular mechanisms that underlie adaptive divergence in complex traits can be assessed in traits like animal venoms where variation in gene sequence and expression levels can be directly linked to functional divergence in phenotypes. We used novel metrics for measuring functional divergence based on amino acid variation to assess the impact of coding sequence evolution, gene duplication and loss, and expression variation on the divergence in venom between sister species in two lineages of pitvipers.

resultsIn both lineages, coding sequence and expression variation made significant contributions to overall functional divergence whereas genic variation was less important. Locus-specific analyses of two multigene families that encode important venom proteins (serine proteases and metalloproteases) showed that (1) There were differences between lineages in the distributions of locus effect size on functional divergence between Sistrurus (many loci with similar effects) and Bothrops (loci with either small or large effects); (2) A small number of loci were under strong positive selection, but only in serine proteases was the intensity of selection positively correlated with contributions to functional divergence in venom. (3) Patterns of overall serine protease and metalloprotease expression differed between lineages, but there was no association between expression levels of individual genes and contributions to divergence.

conclusionsOur results show that the genetic underpinnings of early adaptive divergence in snake venoms are multifaceted and vary across lineages. Broadly, sequence and expression divergence both have substantial effects on functional divergence and each of these mechanisms has greater impacts than genic variation.

Indexed as

Crotalid VenomsEvolution, MolecularGenomeAnimalsBothropsGene DuplicationGenetic VariationMetalloproteasesPhylogenySelection, GeneticSerine ProteasesCrotalid VenomsMetalloproteasesSerine ProteasesBothropsComparative genomicsFunctional variationPhenotypic divergencePitvipersSistrurusVenom

Identifiers

PMID41466268
PMCPMC12752072

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.