1998
DOI: 10.1086/302133
|View full text |Cite
|
Sign up to set email alerts
|

Trading Genes along the Silk Road: mtDNA Sequences and the Origin of Central Asian Populations

Abstract: Central Asia is a vast region at the crossroads of different habitats, cultures, and trade routes. Little is known about the genetics and the history of the population of this region. We present the analysis of mtDNA control-region sequences in samples of the Kazakh, the Uighurs, the lowland Kirghiz, and the highland Kirghiz, which we have used to address both the population history of the region and the possible selective pressures that high altitude has on mtDNA genes. Central Asian mtDNA sequences present f… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

37
274
3
2

Year Published

1999
1999
2018
2018

Publication Types

Select...
6
2
1

Relationship

3
6

Authors

Journals

citations
Cited by 293 publications
(318 citation statements)
references
References 53 publications
37
274
3
2
Order By: Relevance
“…Altogether, these results indicate that the genetic pool of NEAS is related to that of CAS and exhibits signatures of gene flow from multiple sources, while that of SEAS indicates greater isolation and population subdivision, although with a low level of differentiation among populations. Another crucial result related to these observations is the very high level of genetic diversity found in Central Asian populations (Comas et al 1998(Comas et al , 2004Hammer et al 2001;Quintana-Murci et al 2004;Wells et al 2001;Zerjal et al 2002), compatible with their connection to NEAS through gene flow, Central Asia being considered either as a source or as a receiver (Comas et al 1998(Comas et al , 2004Quintana-Murci et al 2004;Zerjal et al 2002) of human migrations.…”
Section: North and South Substructuresmentioning
confidence: 91%
“…Altogether, these results indicate that the genetic pool of NEAS is related to that of CAS and exhibits signatures of gene flow from multiple sources, while that of SEAS indicates greater isolation and population subdivision, although with a low level of differentiation among populations. Another crucial result related to these observations is the very high level of genetic diversity found in Central Asian populations (Comas et al 1998(Comas et al , 2004Hammer et al 2001;Quintana-Murci et al 2004;Wells et al 2001;Zerjal et al 2002), compatible with their connection to NEAS through gene flow, Central Asia being considered either as a source or as a receiver (Comas et al 1998(Comas et al , 2004Quintana-Murci et al 2004;Zerjal et al 2002) of human migrations.…”
Section: North and South Substructuresmentioning
confidence: 91%
“…[2][3][4][5][6][7] The presence of West-Eurasian genetic components in North and East Asia can be interpreted either as the evidence of ancient migration via the northern route 8 or simply as the reflection of recent population admixture. 9,10 However, results of mtDNA analysis in northern Eurasian populations do not support a northern Asian migration route out of Africa, but they do predict that there were at least two migrations into South Siberia, one from East Asia and one from West Eurasia. 6 West Eurasian mtDNA haplogroups found in gene pools of South Siberians (for example, N1e, I4, J1b2, N1a, U4 and X2e) demonstrate an obvious link between populations of Siberia and those of West Asia, the Caucasus and East Europe.…”
Section: Introductionmentioning
confidence: 88%
“…This emphasize the complex background of Northwest Siberian genetic diversity, shaped by recurrent founder effects, admixture and drift in these indigenous populations. Figure 5 Median-joining networks for Eurasian (a) mtDNA U4 sequences (colors for the U4 network are the following: gray (original Khanty and Mansi data with additional reference populations 40,44,45 ); white (Northeast European populations 16,25,46 -48 ) and black (South Siberian populations 12,15,49 grouped with Central Asian populations 50,51 and Central Siberia Yakuts 52 )) and Y chromosome (b) N3 (the N3 network corresponds the following colors: gray (original Khanty and Mansi data); white (Northeast European populations 28,53 ) and black (Central Siberian Yakuts 54 )) and (c) N2 Y-short tandem repeat (STR) haplotypes (nine loci) (the N2 network corresponds the following colors: gray (original Khanty and Mansi data); white (Northeast European populations 11,28 ) and black (South Siberian populations 11 grouped with Northeast Siberian Eskimos 11 )).…”
Section: Mansi Str Haplotypes (Supplementarymentioning
confidence: 99%