Maria C Codlin,Lisa Yeomans,Josefin Stiller,Beatrice Demarchi
{"title":"A library of avian proteins improves palaeoproteomic taxonomic identification and reveals widespread intraspecies variability.","authors":"Maria C Codlin,Lisa Yeomans,Josefin Stiller,Beatrice Demarchi","doi":"10.1038/s41467-025-63886-1","DOIUrl":null,"url":null,"abstract":"Biomineral-associated proteins, such as those found in bone, teeth, and eggshell, have become instrumental for studying ancient life, as they often survive far longer than DNA. Harnessing advancements in avian genomics, we annotate bone and eggshell protein sequences for 112 Anatidae (ducks, geese and swans) species, a biologically complex group of birds that are central to many archaeological and ecological questions. While palaeoproteomics conventionally assumes that protein sequences vary only between-species or above, our research demonstrates widespread evidence for single amino acid polymorphisms (SAPs) occurring within-species, particularly within avian eggshell proteins. Furthermore, we construct a phylogenetic tree from 13 proteins that aligns with mtDNA-based phylogenies, while revealing highly variable topologies for individual protein trees, underscoring the need for caution when using fragmented proteins for taxonomic identification and determining evolutionary relationships. However, with comprehensive taxonomic coverage of Anatidae proteins, clear taxonomic patterns enable reliable identification of bone and eggshell. We demonstrate this application to archaeological material from Teotihuacan, Mexico, and Shubayqa, Jordan. We highlight that extensive curated protein datasets accompanied by rigorous standards for assessing SAPs as taxonomic biomarkers are fundamental for correct taxonomic identification, setting benchmarks for palaeoproteomic applications in archaeology, ecology, and evolutionary biology.","PeriodicalId":19066,"journal":{"name":"Nature Communications","volume":"97 1","pages":"8820"},"PeriodicalIF":15.7000,"publicationDate":"2025-10-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nature Communications","FirstCategoryId":"103","ListUrlMain":"https://doi.org/10.1038/s41467-025-63886-1","RegionNum":1,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Biomineral-associated proteins, such as those found in bone, teeth, and eggshell, have become instrumental for studying ancient life, as they often survive far longer than DNA. Harnessing advancements in avian genomics, we annotate bone and eggshell protein sequences for 112 Anatidae (ducks, geese and swans) species, a biologically complex group of birds that are central to many archaeological and ecological questions. While palaeoproteomics conventionally assumes that protein sequences vary only between-species or above, our research demonstrates widespread evidence for single amino acid polymorphisms (SAPs) occurring within-species, particularly within avian eggshell proteins. Furthermore, we construct a phylogenetic tree from 13 proteins that aligns with mtDNA-based phylogenies, while revealing highly variable topologies for individual protein trees, underscoring the need for caution when using fragmented proteins for taxonomic identification and determining evolutionary relationships. However, with comprehensive taxonomic coverage of Anatidae proteins, clear taxonomic patterns enable reliable identification of bone and eggshell. We demonstrate this application to archaeological material from Teotihuacan, Mexico, and Shubayqa, Jordan. We highlight that extensive curated protein datasets accompanied by rigorous standards for assessing SAPs as taxonomic biomarkers are fundamental for correct taxonomic identification, setting benchmarks for palaeoproteomic applications in archaeology, ecology, and evolutionary biology.
期刊介绍:
Nature Communications, an open-access journal, publishes high-quality research spanning all areas of the natural sciences. Papers featured in the journal showcase significant advances relevant to specialists in each respective field. With a 2-year impact factor of 16.6 (2022) and a median time of 8 days from submission to the first editorial decision, Nature Communications is committed to rapid dissemination of research findings. As a multidisciplinary journal, it welcomes contributions from biological, health, physical, chemical, Earth, social, mathematical, applied, and engineering sciences, aiming to highlight important breakthroughs within each domain.