Diversity of HLA Class I and Class II blocks and conserved extended haplotypes in Lacandon Mayans

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作者
Rodrigo Barquera
Joaquin Zuniga
José Flores-Rivera
Teresa Corona
Bridget S. Penman
Diana Iraíz Hernández-Zaragoza
Manuel Soler
Letisia Jonapá-Gómez
Kalyan C. Mallempati
Petra Yescas
Adriana Ochoa-Morales
Konstantinos Barsakis
José Artemio Aguilar-Vázquez
Maricela García-Lechuga
Michael Mindrinos
María Yunis
Luis Jiménez-Alvarez
Lourdes Mena-Hernández
Esteban Ortega
Alfredo Cruz-Lagunas
Víctor Hugo Tovar-Méndez
Julio Granados
Marcelo Fernández-Viña
Edmond Yunis
机构
[1] Department of Archaeogenetics,
[2] Max Planck Institute for the Science of Human History (MPI-SHH),undefined
[3] Laboratory of Molecular Genetics,undefined
[4] Escuela Nacional de Antropología e Historia (ENAH),undefined
[5] Department of Immunology,undefined
[6] Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas (INER),undefined
[7] Tecnologico de Monterrey,undefined
[8] Escuela de Medicina y Ciencias de la Salud,undefined
[9] Clinical Laboratory of Neurodegenerative Diseases,undefined
[10] Instituto Nacional de Neurología y Neurocirugía “Manuel Velasco Suárez”,undefined
[11] University of Warwick,undefined
[12] School of Life Sciences,undefined
[13] Immunogenetics Unit,undefined
[14] Técnicas Genéticas Aplicadas a la Clínica (TGAC),undefined
[15] Department of Transplantation,undefined
[16] Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán (INCMSZ),undefined
[17] Public Health State Laboratory for Chiapas,undefined
[18] Tuxtla Gutierrez,undefined
[19] Histocompatibility,undefined
[20] Immunogenetics and Disease Profiling Laboratory,undefined
[21] Stanford Blood Center,undefined
[22] Biology Department,undefined
[23] University of Crete,undefined
[24] Department of Neurogenetics and Molecular Biology,undefined
[25] Instituto Nacional de Neurología y Neurocirugía “Manuel Velasco Suárez”,undefined
[26] Department of Pathology,undefined
[27] Clinical Analysis Laboratory,undefined
[28] Unidad Médica Familiar (UMF) No. 23,undefined
[29] Instituto Mexicano del Seguro Social (IMSS),undefined
[30] Stanford Genome Technology Center,undefined
[31] Department of Cancer Immunology and Virology,undefined
[32] Dana Farber Cancer Institute,undefined
[33] Harvard Medical School,undefined
[34] The William Harvey Research Institute,undefined
[35] Barts and London School of Medicine,undefined
[36] Queen Mary University of London,undefined
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摘要
Here we studied HLA blocks and haplotypes in a group of 218 Lacandon Maya Native American using a high-resolution next generation sequencing (NGS) method. We assessed the genetic diversity of HLA class I and class II in this population, and determined the most probable ancestry of Lacandon Maya HLA class I and class II haplotypes. Importantly, this Native American group showed a high degree of both HLA homozygosity and linkage disequilibrium across the HLA region and also lower class II HLA allelic diversity than most previously reported populations (including other Native American groups). Distinctive alleles present in the Lacandon population include HLA-A*24:14 and HLA-B*40:08. Furthermore, in Lacandons we observed a high frequency of haplotypes containing the allele HLA-DRB1*04:11, a relatively frequent allele in comparison with other neighboring indigenous groups. The specific demographic history of the Lacandon population including inbreeding, as well as pathogen selection, may have elevated the frequencies of a small number of HLA class II alleles and DNA blocks. To assess the possible role of different selective pressures in determining Native American HLA diversity, we evaluated the relationship between genetic diversity at HLA-A, HLA-B and HLA-DRB1 and pathogen richness for a global dataset and for Native American populations alone. In keeping with previous studies of such relationships we included distance from Africa as a covariate. After correction for multiple comparisons we did not find any significant relationship between pathogen diversity and HLA genetic diversity (as measured by polymorphism information content) in either our global dataset or the Native American subset of the dataset. We found the expected negative relationship between genetic diversity and distance from Africa in the global dataset, but no relationship between HLA genetic diversity and distance from Africa when Native American populations were considered alone.
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