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Author | Topic: E3b |
alTakruri~ Junior Member Posts: 12 |
posted 05 April 2005 03:05 PM
http://www.ftdna.com/pdf/AJHG_2004_v74_p1023-1034.pdf An excellent report with maps showing distributions in the Will post the report that gives appx dates of mutation when and if Ornella Semino et al Am. J. Hum. Genet. 74:1023–1034, 2004 Origin, Diffusion, and Differentiation of Y-Chromosome Haplogroups E
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alTakruri~ Junior Member Posts: 12 |
posted 05 April 2005 03:30 PM
"The current distributions of the haplogroups can suggest geographical origins, and their TMRCAs provide some constraints on the times of their spread. The M35 lineage (see the phylogeny in fig. 1A for marker locations) is thought to have arisen in East Africa, on the basis of its high frequency and diversity there (Cruciani et al. 2004; Semino et al. 2004), and to have given rise to M81 in North Africa. The TMRCAs for E3b (8.3 KY, 95% CI 5.212.4 KY; or 14.4 KY, 95% CI 9.319.3 KY; table 2) and E3b2 (2.88.2 KY) should thus bracket the spread of E3b2 in North Africa. These times contrast sharply with estimates of 53 ± 21 KYA for the M35 lineage and 32 ± 11 KYA for the M81 lineage, by use of a constant-sized population model, or 30 ± 6 and 19 ± 4 KYA, respectively, by use of an expanding population model (Bosch et al. 2001). They are, however, more in accordance with times of 26.5 KYA (without a useful CI) for the M215 mutation (intermediate between M35 and M96 in the phylogeny; see fig. 1A) and 5.6 KYA for M81 (Cruciani et al. 2004) or of 29.2 ± 4.1 KYA for M35 and 8.6 ± 2.3 KYA for M81 (Semino et al. 2004)." http://www.journals.uchicago.edu/AJHG/journal/issues/v75n2/41184/41184.text.html
[This message has been edited by alTakruri~ (edited 05 April 2005).] IP: Logged |
rasol Member Posts: 2804 |
posted 05 April 2005 04:55 PM
Of interest, among other things is the different frequency of West Asian J in the Oromo [3.8% and the Amhara [35.4%], vs. E3b, [80%] in the Oromo vs. [46%] in the Amhara. Within these two Ethiopian groups there is clearly an inverse relationship between East African E and West Asian J.
Sneaky, but not sneaky enough. Good post. [This message has been edited by rasol (edited 05 April 2005).] IP: Logged |
alTakruri~ Junior Member Posts: 12 |
posted 05 April 2005 04:59 PM
quote: Good point on selected population. There are many tribes or ethnies in IP: Logged |
rasol Member Posts: 2804 |
posted 05 April 2005 05:09 PM
quote:
quote: The Surma live in Ethiopia and Sudan. IP: Logged |
Super car Member Posts: 747 |
posted 05 April 2005 10:17 PM
quote: Other than a loner like Evil, don't know of any other person who talks of a Eurasian origin for E3b. Deepest clades of human Y-Chromosomes are found in both Horn of Africa populations, in particular Ethiopians, and the Khoisans: Semino et al; Ethiopians and Khoisan Share the Deepest Clades of the Human Y-Chromosome Phylogeny : "The genetic structure of 126 Ethiopian and 139 Senegalese Y chromosomes was investigated by a hierarchical analysis of 30 diagnostic biallelic markers selected from the worldwide Y-chromosome genealogy. The present study reveals that (1) only the Ethiopians share with the Khoisan the deepest human Y-chromosome clades (the African-specific Groups I and II) but with a repertoire of very different haplotypes; (2) ***most of the Ethiopians and virtually all the Senegalese belong to Group III***, whose precursor is believed to be involved in the first migration out of Africa; and (3) the Ethiopian Y chromosomes that fall into Groups VI, VIII, and IX may be explained by back migrations from Asia. The first observation confirms the ancestral affinity between the Ethiopians and the Khoisan, which has previously been suggested by both archaeological and genetic findings." Now, of course E3b belongs to Group III:
Go to the high resolution image. Fulvio Cruciani et al.; Phylogeographic Analysis of Haplogroup E3b (E-M215) Y Chromosomes Reveals Multiple Migratory Events Within and Out Of Africa; 2004 E3b originated in sub-Saharan Africa and expanded into the Near East and northern Africa at the end of the Pleistocene (Underhill et al. 2001). E3b lineages would have then been introduced from the Near East into southern Europe by immigrant farmers, during the Neolithic expansion (Hammer et al. 1998; Semino et al. 2000; Underhill et al. 2001). Several observations point to eastern Africa as the homeland for haplogroup E3b, that is, it had :
[This message has been edited by Super car (edited 05 April 2005).] IP: Logged |
Thought2 Member Posts: 1293 |
posted 06 April 2005 02:49 AM
Thought Writes: This was interesting…. Thought Posts:
Haplogroup E3a E3a Haplotype #2 [This message has been edited by Thought2 (edited 06 April 2005).] IP: Logged |
rasol Member Posts: 2804 |
posted 06 April 2005 06:22 AM
Thought: What information do we have about the location and date of the PN2 transition? [ie - prior to the divergance of E3A and E3b] I suspect the desire to make E3A "NorthWest African" will increase as this lineage is discovered more and more often in Europe. [This message has been edited by rasol (edited 06 April 2005).] IP: Logged |
Thought2 Member Posts: 1293 |
posted 06 April 2005 12:15 PM
quote: Thought Writes: Thought Writes: There really aren't many studies differentiating E3a the way they have done with E3b. I imagine this has something to do with the fact that E3b is so prevalent in Europe. In the study by Semino et al, Figure 1 they indicate a TMRCA of 18.8 ky for E3a (from ancestral E3). Senegalese have the highest frequency of E3a. Interestingly enough they are one of the few populations listed with a substantial frequency of M35 as well. More research on E3a is definitely needed. I agree, as more of these lineages pop-up in Europeans they will take a interest in it and attempt to create an ‘explanation’. http://www.ftdna.com/pdf/AJHG_2004_v74_p1023-1034.pdf [This message has been edited by Thought2 (edited 06 April 2005).] IP: Logged |
Thought2 Member Posts: 1293 |
posted 06 April 2005 12:24 PM
Thought Writes: Two new studies:
Phylogeny and antiquity of M macrohaplogroup inferred from complete mt DNA sequence of Indian specific lineages
Abstract (provisional) Background Analysis of human complete mitochondrial DNA sequences has largely contributed to resolve phylogenies and antiquity of different lineages belonging to the majorhaplogroups L, N and M (East-Asian lineages). In the absence of whole mtDNA sequence information of M lineages reported in India that exhibits highest diversity within the sub-continent, the present study was undertaken to provide a detailed analysis of this macrohaplogroup to precisely characterize and unravel the intricate phylogeny of the lineages and to establish the antiquity of M lineages in India. Results The phylogenetic tree constructed from sequencing information of twenty-four whole mtDNA genome revealed novel substitutions in the previously defined M2a and M6 lineages. The most striking feature of this phylogenetic tree is the recognition of two new lineages, M30 and M31, distinguished by transitions at 12007 and 5319, respectively. M30 comprises of M18 and identifies a potential new sub-lineage possessing substitution at 16223 and 16300. It further branches into M30a sub-lineage, defined by 15431 and 195A substitution. The age of M30 lineage was estimated at 33,042 YBP, indicating a more recent expansion time than M2 (49,686 YBP). The M31 branch encompasses the M6 lineage along with the previously defined M3 and M4 lineages. Contradictory to earlier reports, the M5 lineage does not always include a 12477 substitution, and is more appropriately defined by a transversion at 10986A. The phylogenetic tree also identifies a potential new lineage in the M* branch with HVSI sequence as 16223,16325. Substitutions in M25 were in concordance with previous reports. Conclusions This study describes five new basal mutations and recognizes two new lineages, M30 and M31 that substantially contribute to the present understanding of macrohaplogroup M. These two newly erected lineages include the previously independent lineages M18 and M6 as sub-lineages within them, respectively, suggesting that most mt DNA genomes might arise as limited offshoots of M trunk. Furthermore, this study supports the non existence of lineages such as M3 and M4 that are solely defined on the basis of fast mutating control region motifs and hence, establishes the importance of coding region markers for an accurate understanding of the phylogeny. The deep roots of M phylogeny clearly establish the antiquity of Indian lineages, especially M2, as compared to Ethiopian M1 lineage and hence, support an Asian origin of M macrohaplogroup. Human Genetics (Online Early) Genetic evidence in support of a shared Eurasian-North African dairying origin Sean Myles Abstract The process by which pastoralism and agriculture spread from the Fertile Crescent over the past 10,000 years has been the subject of intense investigation by geneticists, linguists and archaeologists. However, no consensus has been reached as to whether this Neolithic transition is best characterized by a demic diffusion (with a significant genetic input from migrating farmers) or a cultural diffusion (without substantial migration of farmers). Milk consumption and thus lactose tolerance are assumed to have spread with pastoralism and we propose that by looking at the relevant mutations in and around the lactase gene in human populations, we can gain insight into the origin(s) and spread of dairying. We genotyped the putatively causal allele for lactose tolerance (–13910T) and constructed haplotypes from several polymorphisms in and around the lactase gene (LCT) in three North African Berber populations and compared our results with previously published data. We found that the frequency of the –13910T allele predicts the frequency of lactose tolerance in several Eurasian and North African Berber populations but not in most sub-Saharan African populations. Our analyses suggest that contemporary Berber populations possess the genetic signature of a past migration of pastoralists from the Middle East and that they share a dairying origin with Europeans and Asians, but not with sub-Saharan Africans. IP: Logged |
Thought2 Member Posts: 1293 |
posted 06 April 2005 12:36 PM
quote: Thought Writes: Before Evil E and his mentor Diekenes get excited I should mention that a Upper Paleolithic origin of M has no bearing on Caucasoids at all. In fact Andaman Islanders may represent the pristine type that carried the M lineage in Asia. Europeans were still somewhat tropically adapted as late as the Mesolithic period. IP: Logged |
Thought2 Member Posts: 1293 |
posted 06 April 2005 12:46 PM
quote: Thought Writes: They sampled three (3) Berber groups. Red Flag right there. In addition, none of us contest the fact that **MODERN** Berbers and Iberians share in a common gene pool based upon mtDNA. Immigration from Eurasia since the Cartheginian period is the most parsimonious explaination for this shared gene pool. IP: Logged |
lamin Member Posts: 223 |
posted 06 April 2005 01:15 PM
Again we have reference to the problematic "sub-Saharan African" concept with reference to lactose intolerance. In fact the Hausa(and many Yoruba) of Nigeria are markedly lactose tolerant and I would imagine the same would hold for pastoral African groups. The Western research mindset is constantly seeking--unless incontrovertible evidence crops up--match certain phenotypical traits with the European world. IP: Logged |
rasol Member Posts: 2804 |
posted 06 April 2005 02:16 PM
quote: The Genetic Origins of the Andaman Islanders IP: Logged |
Thought2 Member Posts: 1293 |
posted 06 April 2005 05:44 PM
quote: Thought Writes: Haplogroup M **may** have entered Africa prior to the Last Glacial Maximum along with U6 and the Y-Chromosome marker R1* and then diverged into the African specific marker M1. In addition it is of interest that early Europeans (Grimaldi Man) and so-called Aurignacian finds from Siberia (where upstream R1* spread as well) have cranial morphologies with greater resemblance to modern "Sub-Saharan" Africans than extant Europeans or NE Asians. From the perspective of history it is of interest to note that the Greeks mentioned two Ethiopias, a eastern Ethiopia in Asia and a western Ethiopia in Africa. This is consistent with the theme of a Andaman Islander type population spreading R1*, U6 and ancestral M lineages back into Africa. "Caucasoids" played no part in this process. Recent studies demonstrating substanial frequencies of M1 as far west in Africa as Guinea-Bissau call for larger sample sizes and more diverse populations studies in Africa to ascertain the shared gene pool of East and West Africans. We have hints of a genetic continuity existing from the Bay of Bengal to the Gulf of Guinea. IP: Logged |
rasol Member Posts: 2804 |
posted 07 April 2005 10:46 AM
Andaman Islander. IP: Logged |
rasol Member Posts: 2804 |
posted 07 April 2005 06:49 PM
Lamin wrote: quote: Group VI on the above map is "J" it is associated with Asiatic semites, including the Cohen Haplotype in the Bantu speaking Lemba of South Africa. IP: Logged |
Thought2 Member Posts: 1293 |
posted 09 April 2005 12:47 AM
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=516768 Most of the extant mtDNA boundaries in South and Southwest Asia were likely shaped during the initial settlement of Eurasia by anatomically modern humans Mait Metspalu et al. “The overwhelming majority of the Iranian mtDNAs have been shown to lie in the West Eurasian domain of the global human mtDNA pool [27,28]. Here we focus on the analysis of mtDNA lineages that are shared between Indians and Iranians and bear signals of pre-Holocene expansion in the region.” “We found haplogroup M ubiquitous at almost 58% among the caste, and 72% among the tribal populations.” “Over 90% of the mtDNAs found in Iran belong to haplogroups HV, TJ, U, N1, N2 and X, commonly found in West Eurasia.” “Compared to India, haplogroup M frequency in Iran is marginally low (5.3%) and there are no distinguished Iranian-specific sub-clades of haplogroup M. All Iranian haplogroup M lineages can be seen as derived from other regional variants of the haplogroup: eleven show affiliation to haplogroup M lineages found in India, twelve in East and Central Asia (D, G, and M8) and one in northeast Africa (M1).” “We found that haplogroup M frequency drops abruptly from about 60% in India to about 5% in Iran, marking the western border of the haplogroup M distribution. A similarly sharp border cuts the distribution of Indian-specific mtDNA haplogroups to the east and to the north of the subcontinent. We therefore propose that the initial mtDNA pool established upon the peopling of South Asia has not been replaced but has rather been reshaped in situ by major demographic episodes in the past and garnished by relatively minor events of gene flow both from the West and the East during more recent chapters of the demographic history in the region.” IP: Logged |
rasol Member Posts: 2804 |
posted 09 April 2005 02:22 PM
We found that haplogroup M frequency drops abruptly from about 60% in India to about 5% in Iran, marking the western border of the haplogroup M distribution. A similarly sharp border cuts the distribution of Indian-specific mtDNA haplogroups to the east and to the north of the subcontinent You are suggesting that this makes it odd, that said haplogroup would again become preponderant in Ethiopia? IP: Logged |
lamin Member Posts: 223 |
posted 09 April 2005 03:02 PM
Could it be that Oppenheimer is correct when he traces the migratory route from East Africa to Australia and Melanesia as passing through India without ever venturing into Eurasia? Note that Melanesians are remarkably African in phenotype despite their DNA trackings. So the question is: what are the M trackings in places like the Adaman Islands, Australasia and Melanesia? IP: Logged |
Super car Member Posts: 747 |
posted 09 April 2005 05:17 PM
quote: Well, if M1 in east Africa is going to be closely related to the haplogroup M which is frequent in the Indian subcontinent, and looking at those distribution patterns above and the distance between the two regions, it would have to be one of an early migration, in which later groups coming to Iranian region altered the gene pool. The alternative would be to eliminate a close relationship between M1 and haplogroup M lineages. IP: Logged |
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