TY - JOUR
T1 - Unraveling Signatures of Local Adaptation among Indigenous Groups from Mexico
AU - García-Ortiz, Humberto
AU - Barajas-Olmos, Francisco
AU - Contreras-Cubas, Cecilia
AU - Reynolds, Austin W.
AU - Flores-Huacuja, Marlen
AU - Snow, Meradeth
AU - Ramos-Madrigal, Jazmín
AU - Mendoza-Caamal, Elvia
AU - Baca, Paulina
AU - López-Escobar, Tomás A.
AU - Bolnick, Deborah A.
AU - Flores-Martínez, Silvia Esperanza
AU - Ortiz-Lopez, Rocio
AU - Kostic, Aleksandar David
AU - Villafan-Bernal, José Rafael
AU - Galaviz-Hernández, Carlos
AU - Centeno-Cruz, Federico
AU - García-Zapién, Alejandra Guadalupe
AU - Monge-Cázares, Tulia
AU - Lazalde-Ramos, Blanca Patricia
AU - Loeza-Becerra, Francisco
AU - Abrahantes-Pérez, María del Carmen
AU - Rangel-Villalobos, Héctor
AU - Sosa-Macías, Martha
AU - Rojas-Martínez, Augusto
AU - Martínez-Hernández, Angélica
AU - Orozco, Lorena
N1 - Publisher Copyright:
© 2022 by the authors.
PY - 2022/12
Y1 - 2022/12
N2 - Few studies have addressed how selective pressures have shaped the genetic structure of the current Native American populations, and they have mostly limited their inferences to admixed Latin American populations. Here, we searched for local adaptation signals, based on integrated haplotype scores and population branch statistics, in 325 Mexican Indigenous individuals with at least 99% Native American ancestry from five previously defined geographical regions. Although each region exhibited its own local adaptation profile, only PPARG and AJAP1, both negative regulators of the Wnt/β catenin signaling pathway, showed significant adaptation signals in all the tested regions. Several signals were found, mainly in the genes related to the metabolic processes and immune response. A pathway enrichment analysis revealed the overrepresentation of selected genes related to several biological phenotypes/conditions, such as the immune response and metabolic pathways, in agreement with previous studies, suggesting that immunological and metabolic pressures are major drivers of human adaptation. Genes related to the gut microbiome measurements were overrepresented in all the regions, highlighting the importance of studying how humans have coevolved with the microbial communities that colonize them. Our results provide a further explanation of the human evolutionary history in response to environmental pressures in this region.
AB - Few studies have addressed how selective pressures have shaped the genetic structure of the current Native American populations, and they have mostly limited their inferences to admixed Latin American populations. Here, we searched for local adaptation signals, based on integrated haplotype scores and population branch statistics, in 325 Mexican Indigenous individuals with at least 99% Native American ancestry from five previously defined geographical regions. Although each region exhibited its own local adaptation profile, only PPARG and AJAP1, both negative regulators of the Wnt/β catenin signaling pathway, showed significant adaptation signals in all the tested regions. Several signals were found, mainly in the genes related to the metabolic processes and immune response. A pathway enrichment analysis revealed the overrepresentation of selected genes related to several biological phenotypes/conditions, such as the immune response and metabolic pathways, in agreement with previous studies, suggesting that immunological and metabolic pressures are major drivers of human adaptation. Genes related to the gut microbiome measurements were overrepresented in all the regions, highlighting the importance of studying how humans have coevolved with the microbial communities that colonize them. Our results provide a further explanation of the human evolutionary history in response to environmental pressures in this region.
KW - AJAP1
KW - Native American populations
KW - PPARG
KW - gut microbiome
KW - local adaptation
UR - http://www.scopus.com/inward/record.url?scp=85144535810&partnerID=8YFLogxK
U2 - 10.3390/genes13122251
DO - 10.3390/genes13122251
M3 - Article
C2 - 36553518
AN - SCOPUS:85144535810
SN - 2073-4425
VL - 13
JO - Genes
JF - Genes
IS - 12
M1 - 2251
ER -