Evidence map›Paper›PMID 41218074›Full record

ArticleMolecular biology and evolution2025

Tandem Duplication of Serpin Genes Yields Functional Variation and Snake Venom Inhibitors.

Meilyn S Ward, Matthew L Holding, Laura M Haynes, Mark J Margres, Marjorie D Matocq, David Ginsburg

Abstract read
In one paragraph

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. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Meilyn S WardLife Sciences Institute, University of Michigan, Ann Arbor, MI, USA.ORCID 0009-0007-1112-9984
Matthew L HoldingLife Sciences Institute, University of Michigan, Ann Arbor, MI, USA.ORCID 0000-0003-3477-3012
Laura M HaynesLife Sciences Institute, University of Michigan, Ann Arbor, MI, USA.ORCID 0000-0002-2237-659X
Mark J MargresDepartment of Integrative Biology, University of South Florida, Tampa, FL, USA.ORCID 0000-0002-6153-6701
Marjorie D MatocqDepartment of Natural Resources & Environmental Science; Program in Ecology, Evolution, and Conservation Biology, University of Nevada Reno, Reno, NV, USA.ORCID 0000-0003-4829-3749
David GinsburgLife Sciences Institute, University of Michigan, Ann Arbor, MI, USA.ORCID 0000-0002-6436-8942

Funding

The Molecular Genetics of HemostasisR35HL171421 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI David Ginsburg · 2024 to 2026
$2.8M
NHLBI NIH HHS R35 HL171421
6 · The paper itself

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.

Indexed as

Gene DuplicationSerpinsSnake VenomsAnimalsDNA Copy Number VariationsEvolution, MolecularPhylogenySerpinsSnake Venomscoevolutionneofunctionalizationpredator-preyresistancerodentserine protease

Identifiers

PMID41218074
PMCPMC12646145

What Socratic holds

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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 Socratic graph.