Distinguishing human ethnic groups by means of sequences from Heliclobacter pylori:: Lessons from Ladakh

被引:117
作者
Wirth, T
Wang, XY
Linz, B
Novick, RP
Lum, JK
Blaser, M
Morelli, G
Falush, D
Achtman, M
机构
[1] Tokyo Womens Med Univ, Shinjuku Ku, Tokyo 1628666, Japan
[2] NYU, Sch Med, Dept Med, New York, NY 10016 USA
[3] NYU, Sch Med, Skirball Inst Biomol Med, New York, NY 10016 USA
[4] Max Planck Inst Infekt Biol, Dept Mol Biol, D-10117 Berlin, Germany
关键词
mtDNA; microsatellites; admixture; human migrations; population genetics;
D O I
10.1073/pnas.0306629101
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The history of mankind remains one of the most challenging fields of study. However, the emergence of anatomically modern humans has been so recent that only a few genetically informative polymorphisms have accumulated. Here, we show that DNA sequences from Helicobacter pylori, a bacterium that colonizes the stomachs of most humans and is usually transmitted within families, can distinguish between closely related human populations and are superior in this respect to classical human genetic markers. H. pylori from Buddhists and Muslims, the two major ethnic communities in Ladakh (India), differ in their population-genetic structure. Moreover, the prokaryotic diversity is consistent with the Buddhists having arisen from an introgression of Tibetan speakers into an ancient Ladakhi population. H. pylori from Muslims contain a much stronger ancestral Ladakhi component, except for several isolates with an Indo-European signature, probably reflecting genetic flux from the Near East. These signatures in H. pylori sequences are congruent with the recent history of population movements in Ladakh, whereas similar signatures in human microsatellites or mtDNA were only marginally significant. H. pylori sequence analysis has the potential to become an important tool for unraveling short-term genetic changes in human populations.
引用
收藏
页码:4746 / 4751
页数:6
相关论文
共 45 条
[41]   Distinguishing migration from isolation using the variance of pairwise differences [J].
Wakeley, J .
THEORETICAL POPULATION BIOLOGY, 1996, 49 (03) :369-386
[42]  
WAKELEY J, 1993, J MOL EVOL, V37, P613
[43]   Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome [J].
Wang, DG ;
Fan, JB ;
Siao, CJ ;
Berno, A ;
Young, P ;
Sapolsky, R ;
Ghandour, G ;
Perkins, N ;
Winchester, E ;
Spencer, J ;
Kruglyak, L ;
Stein, L ;
Hsie, L ;
Topaloglou, T ;
Hubbell, E ;
Robinson, E ;
Mittmann, M ;
Morris, MS ;
Shen, NP ;
Kilburn, D ;
Rioux, J ;
Nusbaum, C ;
Rozen, S ;
Hudson, TJ ;
Lipshutz, R ;
Chee, M ;
Lander, ES .
SCIENCE, 1998, 280 (5366) :1077-1082
[44]   Helicobacter pylori in North and South America before Columbus [J].
Yamaoka, Y ;
Orito, E ;
Mizokami, M ;
Gutierrez, O ;
Saitou, N ;
Kodama, T ;
Osato, MS ;
Kim, JG ;
Ramirez, FC ;
Mahachai, V ;
Graham, DY .
FEBS LETTERS, 2002, 517 (1-3) :180-184
[45]   Worldwide DNA sequence variation in a 10-kilobase noncoding region on human chromosome 22 [J].
Zhao, ZM ;
Jin, L ;
Fu, YX ;
Ramsay, M ;
Jenkins, T ;
Leskinen, E ;
Pamilo, P ;
Trexler, M ;
Patthy, L ;
Jorde, LB ;
Ramos-Onsins, S ;
Yu, N ;
Li, WH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (21) :11354-11358