Genetic Overview of the Maya Populations: Mitochondrial DNA Haplogroups

被引:4
|
作者
Gonzalez-Oliver, Angelica [1 ]
Pineda-Vazquez, Dirce [1 ]
Garfias-Morales, Ernesto [1 ]
De La Cruz-Laina, Isabel [1 ]
Medrano-Gonzalez, Luis [2 ]
Marquez-Morfin, Lourdes [3 ]
Ortega-Munoz, Allan [4 ]
机构
[1] Univ Nacl Autonoma Mexico, Fac Ciencias, Dept Biol Celular, Ciudad Univ, Coyoacan 04510, Ciudad De Mexic, Mexico
[2] Univ Nacl Autonoma Mexico, Fac Ciencias, Dept Biol Evolut, Ciudad De Mexico, Mexico
[3] Escuela Nacl Antropol & Hist, Inst Nacl Antropol & Hist, Ciudad De Mexico, Mexico
[4] Ctr INAH, Chetmal, Quintana Roo, Mexico
关键词
MITOCHONDRIAL DNA; ANCIENT DNA; MITOCHONDRIAL HAPLOGROUPS; MAYA POPULATIONS; INDIGENOUS POPULATIONS; MTDNA HAPLOGROUPS; NATIVE-AMERICANS; MEXICO; HAPLOTYPES; DEMOGRAPHY; DIVERSITY; PATTERNS; SUGGESTS; DISTANCE;
D O I
10.13110/humanbiology.90.4.03
中图分类号
Q98 [人类学];
学科分类号
030303 ;
摘要
We identified mitochondrial DNA haplogroups A, B, C, and Din 75 present-day Maya individuals, 24 Maya individuals of the colonial period, and 1 pre-Columbian Maya individual from Quintana Roo, Mexico. We examined these data together with those of 21 Maya populations reported in the literature, comprising 647 present-day Maya individuals and 71 ancient Maya individuals. A demographic study based on analysis of fertility and endogamy was carried out in two modern Maya populations to identify cultural factors that influence the mitochondrial haplogroup genetic diversity. Most present-day and ancient Maya populations show a distribution pattern of mitochondrial haplogroup frequencies A, C, B, and D in decreasing order, with haplogroup D absent in several populations. Considering only modern Maya populations with at least 50 individuals analyzed, the present-day Tzotzil and Lacandon populations from Chiapas show the highest and lowest genetic diversity, 0.706 and 0.025, respectively. Our results show small genetic differences between the Maya populations, with the exception of the present-day Tojolabal and Lacandon populations from Chiapas. The present-day Lacandon population from Chiapas differs from other Maya populations in showing almost only haplogroup A. This result suggests a long history of isolation and endogamy as well as a possible founder effect inside the Lacandonian rain forest. The contemporary Tojolabal population is the only one with an unusual mitochondrial haplogroup pattern, exhibiting a frequency of haplogroup B higher than A and the absence of haplogroup C. With a small sample size, the pre-Columbian Copan Maya show a high content of haplogroup C and a low frequency of haplogroup D. The genetic homogeneity of the Maya populations is indicative of a common origin and nearly continuous gene flow in the long term within a general isolation of the whole group, in contrast to the Nahua populations that had different origins. Our demographic study showed high fertility rates and high levels of endogamy in the present-day Maya populations from Quintana Roo that are consistent with their general low genetic diversity. We propose that the genetic similarity among ancient and present-day Maya populations persists due to a strong sense of social cohesion and identity that impacts their marriage practices, keeping this cultural group isolated. These factors have constrained gene flow inside the Maya region and have impeded the differentiation among the Maya. Discernment of genetic differentiation within the peninsula is constrained by the lack of sampling documentation in the literature.
引用
收藏
页码:281 / 300
页数:20
相关论文
共 50 条
  • [1] Distribution of mitochondrial DNA haplogroups in the East Asian populations
    Umetsu, K
    Osawa, M
    Yuasa, I
    Adachi, N
    Wei, YH
    Tanaka, M
    ANTHROPOLOGICAL SCIENCE, 2003, 111 (04) : 435 - 435
  • [2] Mitochondrial DNA haplogroups in Amerindian populations from the Gran Chaco
    Demarchi, DA
    Panzetta-Dutari, GM
    Motran, CC
    de Basualdo, MDL
    Marcellino, AJ
    AMERICAN JOURNAL OF PHYSICAL ANTHROPOLOGY, 2001, 115 (03) : 199 - 203
  • [3] Mitochondrial DNA haplogroups
    Rego-Perez, Ignacio
    Fernandez-Moreno, Mercedes
    Fernandez-Lopez, Carlos
    Arenas, Joaquin
    Blanco, Francisco J.
    ARTHRITIS AND RHEUMATISM, 2008, 58 (08): : 2387 - 2396
  • [4] Diversity of Mitochondrial DNA Haplogroups in Ethnic Populations of the Volga–Ural Region
    M. A. Bermisheva
    K. Tambets
    R. Villems
    E. K. Khusnutdinova
    Molecular Biology, 2002, 36 : 802 - 812
  • [5] Diversity of mitochondrial DNA haplogroups in ethnic populations of the Volga-Ural region
    Bermisheva, MA
    Tambets, K
    Villems, R
    Khusnutdinova, EK
    MOLECULAR BIOLOGY, 2002, 36 (06) : 802 - 812
  • [6] Mitochondrial DNA lineage, genetic diversity and population structure of two pre-hispanic Maya populations
    Ochoa Lugo, M. I.
    Perez Ramirez, G.
    Moreno Galeana, M.
    Munoz, M. D. L.
    FEBS JOURNAL, 2014, 281 : 329 - 329
  • [7] Mitochondrial DNA Haplogroups and Susceptibility to Neuroblastoma
    Chang, Xiao
    Bakay, Marina
    Liu, Yichuan
    Glessner, Joseph
    Rathi, Komal S.
    Hou, Cuiping
    Qu, Huiqi
    Vaksman, Zalman
    Nguyen, Kenny
    Sleiman, Patrick M. A.
    Diskin, Sharon J.
    Maris, John M.
    Hakonarson, Hakon
    JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2020, 112 (12): : 1259 - 1265
  • [8] A single multiplex SNaPshot reaction of 42 SNPs to classify admixture populations into mitochondrial DNA haplogroups
    Paneto, G. G.
    Koehnemann, S.
    Martins, J. A.
    Cicarelli, R. M. B.
    Pfeiffer, H.
    FORENSIC SCIENCE INTERNATIONAL GENETICS SUPPLEMENT SERIES, 2011, 3 (01) : E198 - E199
  • [9] Mitochondrial DNA haplogroups and amyotrophic lateral sclerosis
    Patrick F. Chinnery
    Catherine Mowbray
    Hannah Elliot
    Joanna L. Elson
    Hannah Nixon
    Judith Hartley
    Pamela J. Shaw
    Neurogenetics, 2007, 8 : 65 - 67
  • [10] Mitochondrial DNA diversity in indigenous populations of the southern extent of Siberia, and the origins of Native American haplogroups
    Starikovskaya, EB
    Sukernik, RI
    Derbeneva, OA
    Volodko, NV
    Ruiz-Pesini, E
    Torroni, A
    Brown, MD
    Lott, MT
    Hosseini, SH
    Huoponen, K
    Wallace, DC
    ANNALS OF HUMAN GENETICS, 2005, 69 : 67 - 89