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Martinon-Torres, M.

Publications and source records attributed to Martinon-Torres, M..

4 recordsLinked to original sources

Archaeological preservation of amelogenesis pathways

Dental enamel, the hardest mineralised tissue in the human body, has proven to be an excellent source of ancient proteins, which have been found to survive within dental enamel for at least twenty million years. In archaeological and palaeontological contexts, the enamel proteome is generally considered to be rather small, consisting of about twelve proteins, most of which are unique to enamel. During amelogenesis these proteins undergo in vivo digestion by matrix metalloproteinase 20 (MMP20) and kallikrein 4 (KLK4) as well as serine phosphorylation by family with sequence similarity member 20-C (FAM20C) that alter their characteristics. Gaining knowledge of the previously understudied influence of amelogenesis on the archaeological human dental enamel proteome could benefit various palaeoproteomic analysis, especially in an human evolutionary context. Here we present archaeological dental enamel proteomes and explore protein cleavage patterns and sequence coverage to estimate the effects of in vivo digestion, as well as explore phosphorylation patterns. Additionally, we present a new marker based on phosphorylation to estimate genetic sex.

evolutionary biology↗

Palaeoproteomic insights into the deep roots of the cave bear lineage in Europe

Palaeoproteomics has emerged as a powerful tool for reconstructing the evolutionary history of extinct species, particularly when ancient DNA is poorly preserved or beyond recovery. Here, we present the first large-scale enamel proteomic study focused on the cave bear, spanning specimens from the Early to Late Pleistocene. A primary objective was to determine whether the ursid population from level TD4 of Gran Dolina (Sierra de Atapuerca, Spain) belongs to the cave or the brown bear lineage, a long-standing taxonomic debate. We analyzed specimens from the Atapuerca sites, alongside comparative material from other southwestern European localities. Using LC-MS/MS and an acid demineralization protocol without enzymatic digestion, we successfully recovered enamel proteomes from all fossil samples, including the oldest specimens. Protein profiles were obtained for each extinct ursid, enabling the identification of taxonomically informative peptides across multiple individuals per taxon. Notably, two novel single amino acid polymorphisms (SAPs), found in ameloblastin (AMBN) and alpha-1 antitrypsin (SERPINA1), were restricted to Middle and Late Pleistocene cave bears and may represent new phylogenetic markers for this clade. This study provides the first molecular phylogenetic placement of Ursus dolinensis, supporting its basal position within the speloid lineage, consistent with its proposed ancestral status. Our results highlight the strong phylogenetic signal preserved in dental enamel and the exceptional biomolecular preservation at Atapuerca, providing a robust framework for reconstructing the evolutionary history of Ursidae. Moreover, the consistent recovery of systemic proteins, such as serpins, underscores the potential of enamel proteomes to capture not only evolutionary relationships but also physiological signals relevant to extinct ursids. SignificanceThe phylogenetic position of Ursus dolinensis within the Ursidae family has been a subject of long-standing debate. While some authors place it within the speloid lineage, others suggest affinities with arctoid bears. Here, we analyze the bear population from level TD4 of Gran Dolina (Sierra de Atapuerca, Spain) using palaeoproteomic methods for the first time. Molecular evidence supports the inclusion of U. dolinensis within the speloid lineage, in a basal position, supporting its potential ancestral position. These findings extend the evolutionary depth of the speloid clade in Europe and demonstrate the power of enamel palaeoproteomics to resolve deep-time relationships beyond the limits of ancient DNA, revealing the deep evolutionary roots of the lineage.

evolutionary biology↗

Where do the Dmanisi hominins fit on the human evolutionary tree?

Archeological excavations at the site of Dmanisi in the Republic of Georgia have yielded a rich assemblage of hominin fossil remains, as well as lithic artefacts and bones of fossil fauna. The site is considered to be between 1.95 Ma and 1.77 Ma (Gabunia et al. 2000b) and presents us with the first skeletal evidence of hominins to emerge from Africa, a key event in human evolution. Their morphology, and the degree of morphological variation observed among the assemblage, has generated considerable controversy about their affinities and heterogeneity. Here we use parsimony analyses to test the competing hypotheses for Dmanisi hominins employing characters from the cranium, mandible, dentition, and postcranium; and we address anomalies in endocranial volume, dentition and mandibular structure among the assemblage. We propose that the Dmanisi hominins are not Homo erectus, and that two species are represented among the assemblage: one comprises Homo georgicus and the other an as yet unnamed species. Our review of the dating of the Dmanisi site leads us to propose that Homo georgicus was probably present by 1.8 Ma and that the other hominins recovered from the Dmanisi excavations accumulated at some time or times during the reverse polarity of 1.07 Ma and 1.77 Ma. The specific, individual, ages of these hominins remain unknown.

evolutionary biology↗

Automated high-throughput biological sex identification from archaeological human dental enamel using targeted proteomics

Biological sex is key information for archaeological and forensic studies, which can be determined by proteomics. However, lack of a standardised approach for fast and accurate sex identification currently limits the reach of proteomics applications. Here, we introduce a streamlined mass spectrometry (MS)-based workflow for determination of biological sex using human dental enamel. Our approach builds on a minimally invasive sampling strategy by acid etching, a rapid online liquid chromatography (LC) gradient coupled to high-resolution parallel reaction monitoring assay allowing for a throughput of 200 samples-per-day with high quantitative performance enabling confident identification of both males and females. Additionally, we have developed a streamlined data analysis pipeline and integrated it into an R-Shiny interface for ease-of-use. The method was first developed and optimised using modern teeth and then validated in an independent set of deciduous teeth of known sex. Finally, the assay was successfully applied to archaeological material, enabling the analysis of over 300 individuals. We demonstrate unprecedented performance and scalability, speeding up MS analysis by tenfold compared to conventional proteomics-based sex identification methods. This work paves the way for large-scale archaeological or forensic studies enabling the investigation of entire populations rather than focusing on individual high-profile specimens.

biochemistry↗