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Dive into the research topics where Erika Hagelberg is active.

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Featured researches published by Erika Hagelberg.


Proceedings of the Royal society of London. Series B. Biological sciences | 1991

Isolation and characterization of DNA from archaeological bone

Erika Hagelberg; J. B. Clegg

DNA was extracted from human and animal bones recovered from archaeological sites and mitochondrial DNA sequences were amplified from the extracts using the polymerase chain reaction. Evidence is presented that the amplified sequences are authentic and do not represent contamination by extraneous DNA. The results show that significant amounts of genetic information can survive for long periods in bone, and have important implications for evolutionary genetics, anthropology and forensic science.


Proceedings of the Royal Society of London B: Biological Sciences | 1999

Evidence for mitochondrial DNA recombination in a human population of island Melanesia

Erika Hagelberg; Nick Goldman; Pietro Liò; Simon Whelan; Wulf Schiefenhövel; J. B. Clegg; D. K. Bowden

Mitochondrial DNA (mtDNA) analysis has proved useful in studies of recent human evolution and the genetic affinities of human groups of different geographical regions. As part of an extensive survey of mtDNA diversity in present–day Pacific populations, we obtained sequence information of the hypervariable mtDNA control region of 452 individuals from various localities in the western Pacific. The mtDNA types fell into three major groups which reflect the settlement history of the area. Interestingly, we detected an extremely rare point mutation at high frequency in the small island of Nguna in the Melanesian archipelago of Vanuatu. Phylogenetic analysis of the mtDNA data indicated that the mutation was present in individuals of separate mtDNA lineages. We propose that the multiple occurrence of a rare mutation event in one isolated locality is highly improbable, and that recombination between different mtDNA types is a more likely explanation for our observation. If correct, this conclusion has important implications for the use of mtDNA in phylogenetic and evolutionary studies.


Proceedings of the Royal Society of London B: Biological Sciences | 1993

Genetic polymorphisms in prehistoric Pacific islanders determined by analysis of ancient bone DNA.

Erika Hagelberg; J. B. Clegg

A previously characterized Asian-specific mitochondrial DNA (mtDNA) length mutation has been detected in DNA isolated from prehistoric human bones from Polynesia, including Hawaii, Chatham Islands and Society Islands. In contrast, the Asian mutation was absent in skeletal samples from the Melanesian archipelagos of New Britain and Vanuatu and in the oldest samples from Fiji, Tonga and Samoa in the central Pacific (2700—1600 years BP) although it was present in a more recent prehistoric sample from Tonga. These results, augmented by informative DNA sequence data from the hypervariable region of mtDNA, fail to support current views that the central Pacific was settled directly by voyagers from island Southeast Asia, the putative ancestors of modern Polynesians. An earlier occupation by peoples from the neighbouring Melanesian archipelagos seems more likely.


Trends in Genetics | 2003

Recombination or mutation rate heterogeneity? Implications for Mitochondrial Eve

Erika Hagelberg

The study of mitochondrial DNA (mtDNA) has helped to demonstrate the African origin of our species and the relationship between living humans and the Neanderthals. mtDNA data have also been used to establish the time and route of major events in human history, such as the expansion of Neolithic farmers into Europe, and the settlement of the Pacific and the New World. However, it is becoming apparent that mtDNA evolution is more complex than previously believed. Anomalous mutation patterns perturb phylogenetic assumptions based on mtDNA data. Although they are frequently dismissed as sequencing errors or mutation hotspots, some of the anomalies have no satisfactory explanation. The mechanisms behind apparent mutation rate heterogeneity, or even possible mtDNA recombination, remain unknown. These issues need to be addressed, as they have profound consequences for the interpretation of mtDNA data.


Proceedings of the Royal Society B: Biological Sciences , 267 (1461) pp. 2493-2500. (2000) | 2000

Molecular and morphological evidence on the phylogeny of the Elephantidae

Mark G. Thomas; Erika Hagelberg; Hywel B. Jones; Ziheng Yang; Adrian M. Lister

The African and Asian elephants and the mammoth diverged ca. 4–6 million years ago and their phylogenetic relationship has been controversial. Morphological studies have suggested a mammoth–Asian elephant relationship, while molecular studies have produced conflicting results. We obtained cytochrome b sequences of up to 545 base pairs from five mammoths, 14 Asian and eight African elephants. A high degree of polymorphism is detected within species. With a dugong sequence used as the outgroup, parsimony and maximum–likelihood analyses support a mammoth–African elephant clade. As the dugong is a very distant outgroup, we employ likelihood analysis to root the tree with a molecular clock, and use bootstrap and Bayesian analyses to quantify the relative support for different topologies. The analyses support the mammoth–African elephant relationship, although other trees cannot be rejected. Ancestral polymorphisms may have resulted in gene trees differing from the species phylogeny. Examination of morphological data, especially from primitive fossil members, indicates that some supposed synapomorphies between the mammoth and Asian elephant are variable, others convergent or autapomorphous. A mammoth–African elephant relationship is not excluded. Our results highlight the need, in both morphological and molecular phylogenetics, for multiple markers and close attention to within–taxon variation and outgroup selection.


Proceedings of the Royal Society of London B: Biological Sciences | 2000

Evidence for mitochondrial DNA recombination in a human population of island Melanesia: correction

Erika Hagelberg; Nick Goldman; Pietro Liò; Simon Whelan; Wulf Schiefenhövel; J. B. Clegg; D. K. Bowden

We recently presented evidence of mitochondrial DNA recombination in humans based on the observation of a rare mutation in several unrelated human lineages in Nguna, a small island in Vanuatu, island Melanesia. Since then, the mutation has been shown to be an artefact caused by misalignment of the DNA sequences. Our previous conclusion, that the presence of a rare mutation on different haplotypic backgrounds was a consequence of genetic recombination, is no longer tenable for these data.


Philosophical Transactions of the Royal Society B | 2014

Ancient DNA: the first three decades

Erika Hagelberg; Michael Hofreiter; Christine Keyser

When Russell Higuchi, Allan Wilson and co-workers reported the molecular cloning of a small fragment of DNA from a piece of dry tissue of a quagga, an extinct member of the horse family [[1][1]], they could hardly imagine that 30 years later several hundred scientists would meet at The Royal Society


Journal of Experimental Zoology | 2000

Mitochondrial DNA from Myotragus balearicus, an extinct bovid from the Balearic Islands>

Carles Lalueza-Fox; Jaume Bertranpetit; Josep Antoni Alcover; Neil Shailer; Erika Hagelberg

DNA was extracted from teeth and bones of Myotragus balearicus, a bovid that evolved in isolation on the Balearic Islands (Western Mediterranean) from the end of the Miocene, becoming extinct 4,000 years BP, after the arrival of humans in the islands. The numerous morphological apomorphies of Myotragus, most strikingly its dwarfism, frontal eyes, and ever-growing incisors, obscure its phylogenetic relationships with extant bovids. Therefore, the recovery of genetic information from Myotragus is of significant interest to help clarify the taxonomic position of this species. In this study we amplified and sequenced a 95 bp (base pair) fragment of the mtDNA cytochrome b gene from 6,000-year-old specimens of Myotragus. Several experimental controls, such as amino acid analysis, independent reproduction in two different laboratories, and cloning of the PCR product, support the authenticity of the ancient DNA sequence recovered. Phylogenetic comparison with orthologous sequences from supposedly related extant genera (serow, goral, mountain goat, chamois, takin, sheep, goat, Himalayan tahr, arctic musk ox, barbary sheep, blue sheep, and saiga) from the Caprinae subfamily suggests that Myotragus is related to some of these species. However, the real phylogenetic position of Myotragus is difficult to assess, due to the lack of resolution of the present molecular study, which can be partially attributed to the short length of the genetic fragment recovered.


Philosophical Transactions of the Royal Society B | 2014

Mitochondrial DNA variation in the Viking age population of Norway

Gro Bjørnstad; Pontus Skoglund; Pall Olason; Jan Bill; Anders Götherström; Erika Hagelberg

The medieval Norsemen or Vikings had an important biological and cultural impact on many parts of Europe through raids, colonization and trade, from about AD 793 to 1066. To help understand the genetic affinities of the ancient Norsemen, and their genetic contribution to the gene pool of other Europeans, we analysed DNA markers in Late Iron Age skeletal remains from Norway. DNA was extracted from 80 individuals, and mitochondrial DNA polymorphisms were detected by next-generation sequencing. The sequences of 45 ancient Norwegians were verified as genuine through the identification of damage patterns characteristic of ancient DNA. The ancient Norwegians were genetically similar to previously analysed ancient Icelanders, and to present-day Shetland and Orkney Islanders, Norwegians, Swedes, Scots, English, German and French. The Viking Age population had higher frequencies of K*, U*, V* and I* haplogroups than their modern counterparts, but a lower proportion of T* and H* haplogroups. Three individuals carried haplotypes that are rare in Norway today (U5b1b1, Hg A* and an uncommon variant of H*). Our combined analyses indicate that Norse women were important agents in the overseas expansion and settlement of the Vikings, and that women from the Orkneys and Western Isles contributed to the colonization of Iceland.


BMC Evolutionary Biology | 2013

Y Chromosome analysis of prehistoric human populations in the West Liao River Valley, Northeast China

Yinqiu Cui; Hongjie Li; Chao Ning; Ye Zhang; Lu Chen; Xin Zhao; Erika Hagelberg; Hui Zhou

BackgroundThe West Liao River valley in Northeast China is an ecologically diverse region, populated in prehistory by human populations with a wide range of cultures and modes of subsistence. To help understand the human evolutionary history of this region, we performed Y chromosome analyses on ancient human remains from archaeological sites ranging in age from 6500 to 2700 BP.Results47 of the 70 individuals provided reproducible results. They were assigned into five different Y sub-haplogroups using diagnostic single nucleotide polymorphisms, namely N1 (xN1a, N1c), N1c, C/C3e, O3a (O3a3) and O3a3c. We also used 17 Y short tandem repeat loci in the non-recombining portion of the Y chromosome. There appears to be significant genetic differences between populations of the West Liao River valley and adjacent cultural complexes in the prehistoric period, and these prehistoric populations were shown to carry similar haplotypes as present-day Northeast Asians, but at markedly different frequencies.ConclusionOur results suggest that the prehistoric cultural transitions were associated with immigration from the Yellow River valley and the northern steppe into the West Liao River valley. They reveal the temporal continuity of Y chromosome lineages in populations of the West Liao River valley over 5000 years, with a concurrent increase in lineage diversity caused by an influx of immigrants from other populations.

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J. B. Clegg

John Radcliffe Hospital

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Mark G. Thomas

University College London

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Gro Bjørnstad

Norwegian University of Life Sciences

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Pietro Liò

University of Cambridge

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