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Jacques Cinq-Mars
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« on: August 29, 2002, 11:26:11 AM » |
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All,
The following Abstracts should be of interest to people who consider (as all people should) the so-called “initial Peopling of the New World, as part and parcel of a Late Pleistocene and Upper Palaeolithic lengthy and complex human dispersal continuum/process whose biogeographical roots and chronological antecedents lie in Western Beringia and beyond.
While I realize that it is not fair nor cautious to review or criticize papers on the basis of abstracts alone, I feel, nonetheless (not having access to the full papers), that there is a need to come up with a few comments. This, I think, is warranted by the fact that both abstract mention or suggest that the conclusions reached by the authors on the basis of their “molecular” evidence are somehow supported or reinforced by “additional evidence” that, presumably, is, wholly or in part, of an archaeological nature.
In this regard, it appears that the authors of the two papers may have been rather selective (self serving ?) in their choice of archaeologically derived hypotheses or models that deal with the initial or early “peopling” issue. It seems to be evident, for example, that their interpretations both rely on, to a certain extent, and serve to validate, in some circular ways, recent variations on the “short chronology” theme. Nor do they appear to spend much time, if any at all, confronting their views with those of others who, also working with the tools provided by molecular biology, have managed, in recent years to come up with very different conclusions regarding “timing” and number of dispersal events (not to mention evidence coming out of linguistic and biological anthropology studies). While I realize that one can just go so far on the basis of abstracts, I can nevertheless conclude, I think, by saying: So much for integrated, interdisciplinary studies. I hope I am wrong in my assessment, but …
Jacques Cinq-Mars
Am. J. Hum. Genet., 71:187-192, 2002
Report
Mitochondrial Genome Diversity of Native Americans Supports a Single Early Entry of Founder Populations into America
Wilson A. Silva Jr.,1,5 Sandro L. Bonatto, 6 Adriano J. Holanda, 1 Andrea K. Ribeiro-dos-Santos, 7 Beatriz M. Paixão, 1 Gustavo H. Goldman, 2 Kiyoko Abe-Sandes, 1,10 Luis Rodriguez-Delfin, 8 Marcela Barbosa, 2 Maria Luiza Paçó-Larson, 3 Maria Luiza Petzl-Erler, 9 Valeria Valente, 3 Sidney E. B. Santos, 7 and Marco A. Zago1,4
1Center for Cell Therapy and Regional Blood Center, 2 Faculdade de Ciencias Farmaceuticas de Ribeirão Preto, and Departments of 3 Cell and Molecular Biology and Pathogenic Agents and 4 Clinical Medicine, Faculty of Medicine, University of São Paulo, Ribeirão Preto, Brazil; 5 Department of Genetics, Federal University of Para, Santarem, Brazil; 6Centro de Biologia Genomica e Molecular, Pontificia Universidade Catolica do Rio Grande do Sul, Porto Alegre, Brazil; 7 Laboratory of Human and Medical Genetics, University of Para, Belem, Brazil; 8 Unidad de Biologia Molecular, Facultad de Medicina, Universidad Nacional de Trujillo, Trujillo, Peru; 9 Laboratory of Human Molecular Genetics, Department of Genetics, Federal University of Parana, Curitiba, Brazil; and 10 Universidade Estadual do Sudoeste da Bahia, Jequié, Brazil
There is general agreement that the Native American founder populations migrated from Asia into America through Beringia sometime during the Pleistocene, but the hypotheses concerning the ages and the number of these migrations and the size of the ancestral populations are surrounded by controversy. DNA sequence variations of several regions of the genome of Native Americans, especially in the mitochondrial DNA (mtDNA) control region, have been studied as a tool to help answer these questions. However, the small number of nucleotides studied and the nonclocklike rate of mtDNA control-region evolution impose several limitations to these results. Here we provide the sequence analysis of a continuous region of 8.8 kb of the mtDNA outside the D-loop for 40 individuals, 30 of whom are Native Americans whose mtDNA belongs to the four founder haplogroups. Haplogroups A, B, and C form monophyletic clades, but the five haplogroup D sequences have unstable positions and usually do not group together. The high degree of similarity in the nucleotide diversity and time of differentiation (i.e., ?21,000 years before present) of these four haplogroups support a common origin for these sequences and suggest that the populations who harbor them may also have a common history. Additional evidence supports the idea that this age of differentiation coincides with the process of colonization of the New World and supports the hypothesis of a single and early entry of the ancestral Asian population into the Americas.
Am. J. Hum. Genet., 71:415-421, 2002
Report
Analysis of Mitochondrial DNA Diversity in the Aleuts of the Commander Islands and Its Implications for the Genetic History of Beringia
Olga A. Derbeneva, 1 Rem I. Sukernik,1 Natalia V. Volodko,1 Seyed H. Hosseini, 2 Marie T. Lott, 2 and Douglas C. Wallace 2
1Laboratory of Human Molecular Genetics, Institute of Cytology and Genetics, Siberian Division, Russian Academy of Sciences, Novosibirsk, Russia; and 2 Center for Molecular Medicine, Emory University, Atlanta
The Aleuts are aboriginal inhabitants of the Aleutian archipelago, including Bering and Copper (Medny) Islands of the Commanders, and seem to be the survivors of the inhabitants of the southern belt of the Bering Land Bridge that connected Chukotka/Kamchatka and Alaska during the end of the Ice Age. Thirty mtDNA samples collected in the Commanders, as well as seven mtDNA samples from Sireniki Eskimos in Chukotka who belong to the Beringian-specific subhaplogroup D2, were studied through complete sequencing. This analysis has provided evidence that all 37 of these mtDNAs are closely related, since they share the founding haplotype for subhaplogroup D2. We also demonstrated that, unlike the Eskimos and Na-Dene, the Aleuts of the Commanders were founded by a single lineage of haplogroup D2, which had acquired the novel transversion mutation 8910A. The phylogeny of haplogroup D complete sequences showed that (1) the D2 root sequence type originated among the latest inhabitants of Beringia and (2) the Aleut 8910A sublineage of D2 is a part of larger radiation of rooted D2, which gave rise to D2a (Na-Dene), D2b (Aleut), and D2c (Eskimo) sublineages. The geographic specificity and remarkable intrinsic diversity of D2 lineages support the refugial hypothesis, which assumes that the founding population of Eskimo-Aleut originated in Beringan/southwestern Alaskan refugia during the early postglacial period, rather than having reached the shores of Alaska as the result of recent wave of migration from interior Siberia.
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