Interethnic variation of the MMP-9 microsatellite in Amerindian and Mexican Mestizo populations: considerations for genetic association studies

被引:6
作者
Camacho-Mejorado, R. [1 ]
Noris, G. [2 ]
Santana, C. [2 ]
Magana, J. J. [3 ]
Majluf-Cruz, A. [4 ]
Arellano-Galindo, J. [5 ]
De la Pena, A. [6 ,7 ]
Hernandez-Juarez, J. [4 ]
Calderon-Aranda, E. S. [1 ]
Meraz-Rios, M. A. [8 ]
Gomez, R. [1 ]
机构
[1] Natl Polytech Inst Cinvestav IPN, Ctr Res & Adv Studies, Dept Toxicol, Mexico City, DF, Mexico
[2] BIMODI Lab Mol Biol Diagnost, Queretaro, Mexico
[3] Natl Rehabil Inst, Dept Genet, Lab Genom Med, Mexico City, DF, Mexico
[4] Mexican Inst Social Secur, Thrombosis Haemostasis & Atherogenesis Med Res Un, Mexico City, DF, Mexico
[5] Children Hosp Mexico Federico Gomez, Virol Lab, Mexico City, DF, Mexico
[6] Univ Nacl Autonoma Mexico, Fac Med, Dept Pharmacol, Mexico City, DF, Mexico
[7] Natl Inst Cardiol Ignacio Chavez, Thrombosis & Fribrinolysis Lab, Mexico City, DF, Mexico
[8] Natl Polytech Inst Cinvestav IPN, Ctr Res & Adv Studies, Dept Mol Biomed, Mexico City, DF, Mexico
关键词
MMP-9; Polymorphisms; Population genetics; Ethnicity; Mexican Mestizo population; Amerindian; MATRIX-METALLOPROTEINASE-9; PROMOTER; POLYMORPHISMS; ETHNICITY; ADMIXTURE; DISEASE; STRATIFICATION; SUSCEPTIBILITY; AMERICA; IMPACT; RISK;
D O I
10.4238/2015.March.31.24
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
We studied the interethnic variation of the MMP-9 microsatellite in the Mestizo and Amerindian populations using blood samples collected from 435 healthy unrelated individuals from the Central Valley of Mexico. DNA samples were genotyped using the -90 (CA)(12-27) repeat near the MMP transcriptional start site using capillary electrophoresis. Our data were compared with those from African, Asian, and European populations (N = 729). Both Mestizo and Amerindian populations were in Hardy-Weinberg equilibrium (P >= 0.05). However, strong genetic heterogeneity was found within the Mestizo population (94%, P <= 0.0001), which exhibited the highest frequency of Amerindian, African, and European alleles. Likewise, Amerindians showed 6.7% variation among populations (P <= 0.0001), suggesting a genetic substructure potentially associated with linguistic affiliations. These findings were corroborated with principal component and population differentiation analyses, which showed relative proximity among the Mestizos and their historical parental populations: Asian (F-ST >= 0.05), European (F-ST >= 0.09), and African (F-ST >= 0.02). Nevertheless, important differences were found between Mestizo and Nahuas (P <= 0.0001), and between Mestizo and Me'Phaas (P <= 0.0001). These findings highlight the importance of determining local-specific patterns to establish the population variability of MMP-9 and other polymorphic markers. Validation of candidate markers is critical to identifying risk factors; however, this depends on knowledge of population genetic variation, which increases the possibility of finding true causative variants. We also show that dissimilar ethnic backgrounds might lead to spurious associations. Our study provides useful considerations for greater accuracy and robustness in future genetic association studies.
引用
收藏
页码:2929 / 2939
页数:11
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