A new frequent allele is the missing link in the structural polymorphism of the human mannan-binding protein

HO Madsen, P Garred, JAL Kurtzhals, LU Lamm… - Immunogenetics, 1994 - Springer
HO Madsen, P Garred, JAL Kurtzhals, LU Lamm, LP Ryder, S Thiel, A Svejgaard
Immunogenetics, 1994Springer
Human mannan-binding protein (MBP) is a serum lectin participating in the innate immune
defence. Low MBP concentrations are explained by the dominant action of a point mutation
at codon 54 of the MBP gene in Eskimos, partially in Caucasians, but not in Africans. A
previously described point mutation at codon 57 was very frequent (0.23) in East Africans,
low in Caucasians (0.02), and absent in Eskimos. The African population only conformed to
Hardy-Weinberg expectation when assuming the existence of an unknown allele, which was …
Abstract
Human mannan-binding protein (MBP) is a serum lectin participating in the innate immune defence. Low MBP concentrations are explained by the dominant action of a point mutation at codon 54 of the MBP gene in Eskimos, partially in Caucasians, but not in Africans. A previously described point mutation at codon 57 was very frequent (0.23) in East Africans, low in Caucasians (0.02), and absent in Eskimos. The African population only conformed to Hardy-Weinberg expectation when assuming the existence of an unknown allele, which was subsequently found as a point mutation at codon 52. This allele appeared with a relatively high frequency (0.05) in both Africans and Caucasians, but was absent in Eskimos. Hardy-Weinberg equilibrium is now seen in the investigated ethnic groups. All cases of MBP deficiency may be explained by these three variants.
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