Kaspar Hauser's alleged noble origin - New molecular genetic analyses resolve the controversy.

History Molecular genetics Techniques in genetics

Journal

iScience
ISSN: 2589-0042
Titre abrégé: iScience
Pays: United States
ID NLM: 101724038

Informations de publication

Date de publication:
20 Sep 2024
Historique:
received: 15 01 2024
revised: 21 04 2024
accepted: 16 07 2024
medline: 9 9 2024
pubmed: 9 9 2024
entrez: 9 9 2024
Statut: epublish

Résumé

Kaspar Hauser's parentage has been the subject of research and debate for nearly 200 years. As for his possible aristocratic descent through the House of Baden, there is suspicion that he was swapped as a baby, kidnapped, and kept in isolation to bring a collateral lineage to the throne. In the last 28 years, various genetic analyses have been carried out to investigate this possible aristocratic origin. Previous results using less sensitive Sanger and electrophoresis-based methods were contradictory, and moreover, the authenticity of some samples was disputed, thus leaving the question open. Our analyses using modern capture- and whole genome-based massively parallel sequencing techniques reveal that the mitochondrial DNA haplotypes in different samples attributed to Kaspar Hauser were identical, demonstrating authenticity for the first time, and clearly different from the mitochondrial lineage of the House of Baden, which rules out a maternal relationship and thus the widely believed "Prince theory".

Identifiants

pubmed: 39246441
doi: 10.1016/j.isci.2024.110539
pii: S2589-0042(24)01764-4
pmc: PMC11379569
doi:

Types de publication

Journal Article

Langues

eng

Pagination

110539

Informations de copyright

© 2024 The Authors.

Déclaration de conflit d'intérêts

The authors declare no competing interests.

Auteurs

Walther Parson (W)

Institute of Legal Medicine, Medical University of Innsbruck, Innsbruck, Austria.
Forensic Science Program, The Pennsylvania State University, University Park, PA, USA.

Christina Amory (C)

Institute of Legal Medicine, Medical University of Innsbruck, Innsbruck, Austria.

Turi King (T)

Department of Life Sciences, Milner Centre for Evolution, University of Bath, Bath, UK.
Department of Genetics, University of Leicester, Leicester, UK.
School of Archaeology and Ancient History, University of Leicester, Leicester, UK.

Michaela Preick (M)

Evolutionary Adaptive Genomics, University of Potsdam, Potsdam, Germany.

Cordula Berger (C)

Institute of Legal Medicine, Medical University of Innsbruck, Innsbruck, Austria.

Anna König (A)

Institute of Legal Medicine, Medical University of Innsbruck, Innsbruck, Austria.

Gabriela Huber (G)

Institute of Legal Medicine, Medical University of Innsbruck, Innsbruck, Austria.

Katja Anslinger (K)

Institute of Legal Medicine, Ludwig-Maximilians-University, Munich, Germany.

Birgit Bayer (B)

Institute of Legal Medicine, Ludwig-Maximilians-University, Munich, Germany.

Gottfried Weichhold (G)

Thermo Fisher Scientific, Munich, Germany.

Timo Sänger (T)

Institute of Forensic Medicine, Medical Center, University of Freiburg and Faculty of Medicine, University of Freiburg, Freiburg, Germany.

Sabine Lutz-Bonengel (S)

Institute of Forensic Medicine, Medical Center, University of Freiburg and Faculty of Medicine, University of Freiburg, Freiburg, Germany.

Heidi Pfeiffer (H)

Institute of Legal Medicine, University Hospital Münster, Münster, Germany.

Michael Hofreiter (M)

Evolutionary Adaptive Genomics, University of Potsdam, Potsdam, Germany.

Dietmar Pfründer (D)

Private Scholar, Gaiberg, Germany.

Carsten Hohoff (C)

Institute of Legal Medicine, University Hospital Münster, Münster, Germany.
Privatinstitut für Forensische Molekulargenetik GmbH, Emsdetten, Germany.
Institut für forensische Genetik, Münster, Germany.

Bernd Brinkmann (B)

Institute of Legal Medicine, University Hospital Münster, Münster, Germany.
Institut für forensische Genetik, Münster, Germany.

Classifications MeSH