A worldwide correlation of lactase persistence phenotype and genotypes

被引:211
作者
Itan, Yuval [1 ,2 ]
Jones, Bryony L. [1 ]
Ingram, Catherine J. E. [1 ]
Swallow, Dallas M. [1 ]
Thomas, Mark G. [1 ,2 ,3 ]
机构
[1] UCL, Res Dept Genet Evolut & Environm, London WC1E 6BT, England
[2] UCL, CoMPLEX Ctr Math & Phys Life Sci & Expt Biol, London WC1E 6BT, England
[3] UCL, AHRC Ctr Evolut Cultural Div, Inst Archaeol, London WC1H 0PY, England
基金
英国生物技术与生命科学研究理事会;
关键词
ADULT LACTOSE-MALABSORPTION; ACTIVITY IN-VITRO; PREVALENCE; INTOLERANCE; HYPOLACTASIA; DEFICIENCY; VARIANT; POPULATIONS; TOLERANCE; EVOLUTION;
D O I
10.1186/1471-2148-10-36
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: The ability of adult humans to digest the milk sugar lactose - lactase persistence - is a dominant Mendelian trait that has been a subject of extensive genetic, medical and evolutionary research. Lactase persistence is common in people of European ancestry as well as some African, Middle Eastern and Southern Asian groups, but is rare or absent elsewhere in the world. The recent identification of independent nucleotide changes that are strongly associated with lactase persistence in different populations worldwide has led to the possibility of genetic tests for the trait. However, it is highly unlikely that all lactase persistence-associated variants are known. Using an extensive database of lactase persistence phenotype frequencies, together with information on how those data were collected and data on the frequencies of lactase persistence variants, we present a global summary of the extent to which current genetic knowledge can explain lactase persistence phenotype frequency. Results: We used surface interpolation of Old World lactase persistence genotype and phenotype frequency estimates obtained from all available literature and perform a comparison between predicted and observed trait frequencies in continuous space. By accommodating additional data on sample numbers and known false negative and false positive rates for the various lactase persistence phenotype tests (blood glucose and breath hydrogen), we also apply a Monte Carlo method to estimate the probability that known lactase persistence-associated allele frequencies can explain observed trait frequencies in different regions. Conclusion: Lactase persistence genotype data is currently insufficient to explain lactase persistence phenotype frequency in much of western and southern Africa, southeastern Europe, the Middle East and parts of central and southern Asia. We suggest that further studies of genetic variation in these regions should reveal additional nucleotide variants that are associated with lactase persistence.
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页数:11
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