The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
Tandem Duplication of Serpin Genes Yields Functional Variation and Snake Venom Inhibitors
Open accessPublished version of a preprint
Abstract
Tandem duplication of genes can play a critical role in the evolution of functional novelty, yet our understanding is limited concerning the role of gene duplication in coevolution between species. Much is known about the evolution and function of tandemly duplicated snake venom genes, however, the potential of gene duplication to fuel venom resistance within prey species is poorly understood. The SERPINA subfamily of genes produces globular serine protease inhibitors and carrier molecules, and SERPINA1 has previously been shown to inhibit snake venom serine proteases. In this study, we characterize patterns of duplication within the tandem array of SERPINA, documenting trends in copy number evolution between species. We find the hallmarks of rapid birth-death evolution of SERPINA1-like and SERPINA3-like genes within and between rodent lineages, and evidence for diversifying selection acting on rodent genes. To explore the functional significance of copy number evolution, we recombinantly expressed the full set of 12 paralogous duplicates of SERPINA3 found in the genome of the Big-eared woodrat (Neotoma macrotis), a species known for resistance to protease-rich rattlesnake venoms. Two SERPINA3 paralogs inhibited venom serine proteases, indicating that these proteins may serve as resistance factors. In addition, functional variation is apparent among paralogs, including neofunctionalization to inhibit both chymotrypsin-like and trypsin-like proteases simultaneously for one venom-inhibiting paralog. Our results provide further evidence that the rapid evolution of SERPINA1 and SERPINA3 gene copy number across rodents has adaptive potential by producing functionally diverse venom inhibitors.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Highly accurate protein structure prediction with AlphaFold
Jumper, J., Evans, R., Pritzel, A., Green, T., Figurnov, M., Ronneberger, O., Tunyasuvunakool, K., Bates, R., Žídek, A., Potapenko, A., et al. (2021) · Nature · doi:10.1038/s41586-021-03819-2 · Cited by 43,764
Flagged first, then by citations
Research works printed but not linked: 71
- Almagro Armenteros, 2019, Signalp 5.0 improves signal peptide predictions using deep neural networks, Nat Biotechnol., 37, 420, 10.1038/s41587-019-0036-z · DOI
- Altschul, 1990, Basic local alignment search tool, J Mol Biol., 215, 403, 10.1016/S0022-2836(05)80360-2 · DOI · Paper page
- Alvarez-Buylla, 2023, Binding and sequestration of poison frog alkaloids by a plasma globulin, eLife, 12, e85096, 10.7554/eLife.85096 · DOI · Paper page
- Antonovics, 2013, The origin of specificity by means of natural selection: evolved and nonhost resistance in host–pathogen interactions, Evolution, 67, 1, 10.1111/j.1558-5646.2012.01793.x · DOI
- Armstrong, 1999, α2-macroglobulin: an evolutionarily conserved arm of the innate immune system, Developmental & Comparative Immunology, Invertebrate Immunity, 23, 375, 10.1016/S0145-305X(99)00018-X · DOI
- Balchan, 2024, A plethora of rodents: rattlesnake predators generate unanticipated patterns of venom resistance in a grassland ecosystem, Toxicon X., 21, 100179, 10.1016/j.toxcx.2023.100179 · DOI
- Barbour, 2002, Functional diversification during evolution of the murine α1-proteinase inhibitor family: role of the hypervariable reactive center loop, Mol Biol Evol., 19, 718, 10.1093/oxfordjournals.molbev.a004130 · DOI
- Benkman, 2003, Reciprocal selection causes a coevolutionary arms race between crossbills and lodgepole pine, Am Nat, 162, 182, 10.1086/376580 · DOI
- Biardi, 2000, California ground squirrel (Spermophilus beecheyi) blood sera inhibits crotalid venom proteolytic activity, Toxicon, 38, 713, 10.1016/S0041-0101(99)00179-8 · DOI
- Blanquart, 2013, A practical guide to measuring local adaptation, Ecol Lett., 16, 1195, 10.1111/ele.12150 · DOI
- Brodie, 2005, Parallel arms races between garter snakes and newts involving tetrodotoxin as the phenotypic interface of coevolution, J Chem Ecol, 31, 343, 10.1007/s10886-005-1345-x · DOI
- Brodie, 2002, The evolutionary response of predators to dangerous prey: hotspots and coldspots in the geographic mosaic of coevolution between garter snakes and newts, Evolution, 56, 2067, 10.1111/j.0014-3820.2002.tb00132.x · DOI
- Brovkina, 2023, Emergence and influence of sequence bias in evolutionarily malleable, mammalian tandem arrays, BMC Biol, 21, 179, 10.1186/s12915-023-01673-4 · DOI
- Casewell, 2013, Complex cocktails: the evolutionary novelty of venoms, Trends Ecol Evol., 28, 219, 10.1016/j.tree.2012.10.020 · DOI
- Cavalcante, 2022, A fingerprint of plasma proteome alteration after local tissue damage induced by Bothrops leucurus snake venom in mice, J Proteomics, 253, 104464, 10.1016/j.jprot.2021.104464 · DOI
- Cerqueira de Araujo, 2025, Genome sequences of four Ixodes species expands understanding of tick evolution, BMC Biol., 23, 17, 10.1186/s12915-025-02121-1 · DOI
- Chernykh, 2023, Position-specific N- and O-glycosylation of the reactive centre loop impacts neutrophil elastase-mediated proteolysis of corticosteroid-binding globulin, J Biol Chem., 300, 105519, 10.1016/j.jbc.2023.105519 · DOI
- Demuth, 2009, The life and death of gene families, BioEssays, 31, 29, 10.1002/bies.080085 · DOI
- Denardo, 2023, Probing of the reactive center loop region of alpha-1-antitrypsin by mutagenesis predicts new type-2 dysfunctional variants, Cell Mol Life Sci., 81, 6, 10.1007/s00018-023-05059-1 · DOI
- de Wit, 1982, Resistance of the prairie vole (Microtus ochrogaster) and the woodrat (Neotoma floridana), in Kansas, to venom of the Osage copperhead (Agkistrodon contortrix phaeogaster), Toxicon, 20, 709, 10.1016/0041-0101(82)90119-2 · DOI
- de Wit, 1987, Venom resistance in the Hedgehog, Erinaceus europaeus: purification and identification of macroglobulin inhibitors as plasma antihemorrhagic factors, Toxicon, 25, 315, 10.1016/0041-0101(87)90260-1 · DOI
- Dowell, 2016, The deep origin and recent loss of venom toxin genes in rattlesnakes, Curr Biol., 26, 2434, 10.1016/j.cub.2016.07.038 · DOI
- Edgar, 2004, MUSCLE: multiple sequence alignment with high accuracy and high throughput, Nucleic Acids Res, 32, 1792, 10.1093/nar/gkh340 · DOI · Paper page
- Forsyth, 2003, A review and comparison of the murine α1-antitrypsin and α1-antichymotrypsin multigene clusters with the human clade A serpins, Genomics, 81, 336, 10.1016/S0888-7543(02)00041-1 · DOI
- Gettins, 2002, Serpin structure, mechanism, and function, Chem Rev., 102, 4751, 10.1021/cr010170+ · DOI
- Gettins, 2009, Exosite determinants of serpin specificity, J Biol Chem, 284, 20441, 10.1074/jbc.R800064200 · DOI
- Gibbs, 2020, The molecular basis of venom resistance in a rattlesnake-squirrel predator-prey system, Mol Ecol., 29, 2871, 10.1111/mec.15529 · DOI
- Guiher, 2008, Demographic and phylogeographic histories of two venomous North American snakes of the genus Agkistrodon, Mol Phylogenet Evol., 48, 543, 10.1016/j.ympev.2008.04.008 · DOI
- Hahn, 2009, Distinguishing among evolutionary models for the maintenance of gene duplicates, J Hered, 100, 605, 10.1093/jhered/esp047 · DOI
- Haynes, 2025, High-throughput amino acid-level characterization of the interactions of plasminogen activator inhibitor-1 with variably divergent proteases, Protein Sci., 34, e70088, 10.1002/pro.70088 · DOI
- Heit, 2013, Update of the human and mouse SERPINgene superfamily, Hum Genomics., 7, 22, 10.1186/1479-7364-7-22 · DOI
- Holding, 2016, Venom resistance as a model for understanding the molecular basis of complex coevolutionary adaptations, Integr Comp Biol., 56, 1032, 10.1093/icb/icw082 · DOI
- Horvath, 2005, The murine orthologue of human antichymotrypsin: a structural paradigm for clade A3 serpins*, J Biol Chem., 280, 43168, 10.1074/jbc.M505598200 · DOI
- Huntington, 2011, Serpin structure, function and dysfunction, J Thromb Haemost., 9, 26, 10.1111/j.1538-7836.2011.04360.x · DOI
- Itoh, 1988, Organization of the gene for batroxobin, a thrombin-like snake venom enzyme. Homology with the trypsin/kallikrein gene family, J Biol Chem., 263, 7628, 10.1016/S0021-9258(18)68544-8 · DOI
- Keil, 2012, Specificity of proteolysis
- Kim, 2019, Graph-based genome alignment and genotyping with HISAT2 and HISAT-genotype, Nat Biotechnol, 37, 907, 10.1038/s41587-019-0201-4 · DOI · Paper page
- Kosakovsky Pond, 2006, GARD: a genetic algorithm for recombination detection, Bioinformatics, 22, 3096, 10.1093/bioinformatics/btl474 · DOI
- Kumar, 2022, TimeTree 5: an expanded resource for species divergence times, Mol Biol Evol., 39, msac174, 10.1093/molbev/msac174 · DOI
- Lallemand, 2020, An overview of duplicated gene detection methods: why the duplication mechanism has to be accounted for in their choice, Genes (Basel), 11, 1046, 10.3390/genes11091046 · DOI
- Lawrence, 1995, Serpin-protease complexes are trapped as stable acyl-enzyme intermediates (*), J Biol Chem., 270, 25309, 10.1074/jbc.270.43.25309 · DOI
- Manea, 2007, Mass spectrometric identification of the trypsin cleavage pathway in lysyl-proline containing oligotuftsin peptides, J Pept Sci, 13, 227, 10.1002/psc.836 · DOI
- Margres, 2017, Quantity, not quality: rapid adaptation in a polygenic trait proceeded exclusively through expression differentiation, Mol Biol Evol., 34, 3099, 10.1093/molbev/msx231 · DOI
- Markland, 1998, Snake venoms and the hemostatic system, Toxicon, 36, 1749, 10.1016/S0041-0101(98)00126-3 · DOI
- Morel, 2020, GeneRax: a tool for species-tree-aware maximum likelihood-based gene family tree inference under gene duplication, transfer, and loss, Mol Biol Evol, 37, 2763, 10.1093/molbev/msaa141 · DOI
- Murrell, 2012, Detecting individual sites subject to episodic diversifying selection, PLoS Genet., 8, e1002764, 10.1371/journal.pgen.1002764 · DOI · Paper page
- Murrell, 2015, Gene-wide identification of episodic selection, Mol Biol Evol, 32, 1365, 10.1093/molbev/msv035 · DOI
- Ochoa, 2023, Genetic characterization of potential venom resistance proteins in California ground squirrels (Otospermophilus beecheyi) using transcriptome analyses, J Exp Zool B Mol Dev Evol., 340, 259, 10.1002/jez.b.23145 · DOI
- Omori-Satoh, 2000, The antihemorrhagic factor, erinacin, from the European hedgehog (Erinaceus europaeus), a metalloprotease inhibitor of large molecular size possessing ficolin/opsonin P35 lectin domains, Toxicon, 38, 1561, 10.1016/S0041-0101(00)00090-8 · DOI
- Patschull, 2011, Therapeutic target-site variability in α1-antitrypsin characterized at high resolution, Acta Cryst F, 67, 1492, 10.1107/S1744309111040267 · DOI
- Penel, 2022, Thirdkind: displaying phylogenetic encounters beyond 2-level reconciliation, Bioinformatics, 38, 2350, 10.1093/bioinformatics/btac062 · DOI
- Perez, 1978, Resistance of woodrats (Neotoma micropus) to Crotalus atrox venom, Toxicon, 16, 198, 10.1016/0041-0101(78)90039-9 · DOI
- Polanowska, 1998, Specificity of human cathepsin G, Biochimica et Biophysica Acta (BBA)—Protein Structure and Molecular Enzymology, 1386, 189, 10.1016/S0167-4838(98)00085-5 · DOI
- Pomento, 2016, No safety in the trees: local and species-level adaptation of an arboreal squirrel to the venom of sympatric rattlesnakes, Toxicon, 118, 149, 10.1016/j.toxicon.2016.05.003 · DOI
- Pond, 2005, Hyphy: hypothesis testing using phylogenies, Bioinformatics, 21, 676, 10.1093/bioinformatics/bti079 · DOI · Paper page
- Rheaume, 1994, Evolution of murine α1-proteinase inhibitors: gene amplification and reactive center divergence, J Mol Evol, 38, 121, 10.1007/BF00166159 · DOI
- Riewald, 1996, Human cytoplasmic antiproteinase neutralizes rapidly and efficiently chymotrypsin and trypsin-like proteases utilizing distinct reactive site residues*, J Biol Chem., 271, 14526, 10.1074/jbc.271.24.14526 · DOI
- Robinson, 2021, Phenotypic and functional variation in venom and venom resistance of two sympatric rattlesnakes and their prey, J Evol Biol., 34, 1447, 10.1111/jeb.13907 · DOI
- Sayers, 2022, Database resources of the national center for biotechnology information, Nucleic Acids Res, 50, D20, 10.1093/nar/gkab1112 · DOI · Paper page
- Serrano, 2013, The long road of research on snake venom serine proteinases, Toxicon, 62, 19, 10.1016/j.toxicon.2012.09.003 · DOI
- Spence, 2021, A comprehensive phylogenetic analysis of the serpin superfamily, Mol Biol Evol, 38, 2915, 10.1093/molbev/msab081 · DOI
- The UniProt Consortium, 2023, UniProt: the universal protein knowledgebase in 2023, Nucleic Acids Res., 51, D523, 10.1093/nar/gkac1052 · DOI · Paper page
- Thompson, 1994, CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice, Nucleic Acids Res., 22, 4673, 10.1093/nar/22.22.4673 · DOI · Paper page
- Thompson, 2005, Coevolution: the geographic mosaic of coevolutionary arms races, Curr Biol., 15, R992, 10.1016/j.cub.2005.11.046 · DOI
- Thorpe, 2018, Extended cleavage specificity of human neutrophil cathepsin G: a low activity protease with dual chymase and tryptase-type specificities, PLoS One, 13, e0195077, 10.1371/journal.pone.0195077 · DOI
- Toju, 2008, Fine-scale local adaptation of weevil mouthpart length and camellia pericarp thickness: altitudinal gradient of a putative arms race, Evolution, 62, 1086, 10.1111/j.1558-5646.2008.00341.x · DOI
- Wang, 2014, Origin of serpin-mediated regulation of coagulation and blood pressure, PLoS One, 9, e97879, 10.1371/journal.pone.0097879 · DOI
- Whittington, 2018, A single mutation unlocks cascading exaptations in the origin of a potent pitviper neurotoxin, Mol Biol Evol., 35, 887, 10.1093/molbev/msx334 · DOI
- Wu, 2023, Parasitoid serpins evolve novel functions to manipulate host homeostasis, Mol Biol Evol., 40, msad269, 10.1093/molbev/msad269 · DOI
- Wüster, 1992, Population systematics of Russell's viper: a multivariate study, Biol J Linn Soc Lond., 47, 97, 10.1111/j.1095-8312.1992.tb00658.x · DOI
- Yang, 2024, Host and venom evolution in parasitoid wasps: does independently adapting to the same host shape the evolution of the venom gland transcriptome?, BMC Biol., 22, 174, 10.1186/s12915-024-01974-2 · DOI
Metadata
- Authors
- Ward, M. S., Holding, M. L., Haynes, L. M., Margres, M. J., Matocq, M. D., & Ginsburg, D.
- Affiliations
- University of Michigan (US)
- University of South Florida (US)
- University of Nevada, Reno (US)
- Corresponding author
- Holding, Matthew L
- ORCID
- Venue
- Molecular Biology and Evolution
- Publisher
- Oxford University Press (OUP)
- Published
- 2025-10-29
- Volume
- 42
- Issue
- 11
- ISSN
- 0737-4038 (ISSN-L)
- 1537-1719
- PMC
- PMC11741322
- OpenAlex
- W4416665694
- Cited by
- 3
- References
- 1
- Citations by year
- 2026: 2 · 2025: 1
- FWCI
- 1.76
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Molecular Biology and Evolution (publishedVersion, cc-by)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- PubMed Central (submittedVersion, cc-by-nc-nd)
- Funders
- National Institutes of Health (1r35hl171421-01)
- National Heart, Lung, and Blood Institute (R35 HL171421)
- Topics
- Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Toxicology › Venomous Animal Envenomation and Studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Chromosomal and Genetic Variations
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Evolution and Genetic Dynamics
- Keywords
- tandem gene duplication, SERPINA1, alpha-1-antichymotrypsin, copy number evolution, diversifying selection, neofunctionalization, Neotoma macrotis, rattlesnake venom, paralogs
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review