Population studies of the human V kappa A18 gene polymorphism in Caucasians, blacks and Eskimos. New functional alleles and evidence for evolutionary selection of a more restricted antibody repertoire

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Population studies of the human V kappa A18 gene polymorphism in Caucasians, blacks and Eskimos. New functional alleles and evidence for evolutionary selection of a more restricted antibody repertoire. / Juul, L; Hougs, L; Andersen, V; Garred, P; Ryder, L; Svejgaard, A; Høgh, B; Lamm, L; Graugaard, B; Barington, T.

In: Tissue Antigens, Vol. 49, No. 6, 06.1997, p. 595-604.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Juul, L, Hougs, L, Andersen, V, Garred, P, Ryder, L, Svejgaard, A, Høgh, B, Lamm, L, Graugaard, B & Barington, T 1997, 'Population studies of the human V kappa A18 gene polymorphism in Caucasians, blacks and Eskimos. New functional alleles and evidence for evolutionary selection of a more restricted antibody repertoire', Tissue Antigens, vol. 49, no. 6, pp. 595-604.

APA

Juul, L., Hougs, L., Andersen, V., Garred, P., Ryder, L., Svejgaard, A., Høgh, B., Lamm, L., Graugaard, B., & Barington, T. (1997). Population studies of the human V kappa A18 gene polymorphism in Caucasians, blacks and Eskimos. New functional alleles and evidence for evolutionary selection of a more restricted antibody repertoire. Tissue Antigens, 49(6), 595-604.

Vancouver

Juul L, Hougs L, Andersen V, Garred P, Ryder L, Svejgaard A et al. Population studies of the human V kappa A18 gene polymorphism in Caucasians, blacks and Eskimos. New functional alleles and evidence for evolutionary selection of a more restricted antibody repertoire. Tissue Antigens. 1997 Jun;49(6):595-604.

Author

Juul, L ; Hougs, L ; Andersen, V ; Garred, P ; Ryder, L ; Svejgaard, A ; Høgh, B ; Lamm, L ; Graugaard, B ; Barington, T. / Population studies of the human V kappa A18 gene polymorphism in Caucasians, blacks and Eskimos. New functional alleles and evidence for evolutionary selection of a more restricted antibody repertoire. In: Tissue Antigens. 1997 ; Vol. 49, No. 6. pp. 595-604.

Bibtex

@article{2b3e2a71619040e5ab800236cffb3a8e,
title = "Population studies of the human V kappa A18 gene polymorphism in Caucasians, blacks and Eskimos. New functional alleles and evidence for evolutionary selection of a more restricted antibody repertoire",
abstract = "Immunoglobulin gene polymorphisms are interesting because they reflect differences in the available antibody repertoire which may affect the susceptibility to specific infections. Until recently, the human V kappa gene, A18, was known as a nonfunctional gene only. In this study, we cloned and sequenced four apparently functional alleles and determined the gene frequencies in three well-defined populations: Danish Caucasians, eastern Greenland Eskimos and Mozambican blacks. The A18b allele that was recently described in Native American Navajos by Atkinson et al. was found in all three populations with gene frequencies of 8%, 45% and 23% in Caucasians, Eskimos and blacks, respectively. Conversely, the frequencies of the nonfunctional A18a allele were 92%, 55% and 57%. Further, three new A18 alleles, c, d, and e were found exclusively in blacks, among whom they had an total frequency of 19%. These data indicate that both the A18a and A18b alleles originated before the diversification of Africans and non-Africans 90,000 years ago, whereas the A18c, A18d and A18e alleles may have a more recent origin. The functionality of the A18b allele was documented by the demonstration of properly rearranged and somatically hypermutated A18b messenger RNA present in the blood lymphocytes of individuals carrying this allele. The expression clearly exceeded that of a known functional V gene, A2, indicating that functional A18 alleles contribute significantly to the available antibody repertoire. In this context, it is surprising that the functional A18b allele apparently has been negatively selected in the Caucasian population, among whom 85% completely lack a functional gene.",
keywords = "African Continental Ancestry Group/genetics, Alleles, Amino Acid Sequence, Base Sequence, Cloning, Molecular, DNA, Complementary, Denmark, European Continental Ancestry Group/genetics, Gene Expression, Humans, Immunoglobulin Variable Region/genetics, Immunoglobulin kappa-Chains/genetics, Inuits/genetics, Molecular Sequence Data, Mozambique, Polymerase Chain Reaction, Polymorphism, Genetic, Polymorphism, Restriction Fragment Length, RNA, Messenger",
author = "L Juul and L Hougs and V Andersen and P Garred and L Ryder and A Svejgaard and B H{\o}gh and L Lamm and B Graugaard and T Barington",
year = "1997",
month = jun,
language = "English",
volume = "49",
pages = "595--604",
journal = "HLA",
issn = "2059-2302",
publisher = "Wiley-Blackwell",
number = "6",

}

RIS

TY - JOUR

T1 - Population studies of the human V kappa A18 gene polymorphism in Caucasians, blacks and Eskimos. New functional alleles and evidence for evolutionary selection of a more restricted antibody repertoire

AU - Juul, L

AU - Hougs, L

AU - Andersen, V

AU - Garred, P

AU - Ryder, L

AU - Svejgaard, A

AU - Høgh, B

AU - Lamm, L

AU - Graugaard, B

AU - Barington, T

PY - 1997/6

Y1 - 1997/6

N2 - Immunoglobulin gene polymorphisms are interesting because they reflect differences in the available antibody repertoire which may affect the susceptibility to specific infections. Until recently, the human V kappa gene, A18, was known as a nonfunctional gene only. In this study, we cloned and sequenced four apparently functional alleles and determined the gene frequencies in three well-defined populations: Danish Caucasians, eastern Greenland Eskimos and Mozambican blacks. The A18b allele that was recently described in Native American Navajos by Atkinson et al. was found in all three populations with gene frequencies of 8%, 45% and 23% in Caucasians, Eskimos and blacks, respectively. Conversely, the frequencies of the nonfunctional A18a allele were 92%, 55% and 57%. Further, three new A18 alleles, c, d, and e were found exclusively in blacks, among whom they had an total frequency of 19%. These data indicate that both the A18a and A18b alleles originated before the diversification of Africans and non-Africans 90,000 years ago, whereas the A18c, A18d and A18e alleles may have a more recent origin. The functionality of the A18b allele was documented by the demonstration of properly rearranged and somatically hypermutated A18b messenger RNA present in the blood lymphocytes of individuals carrying this allele. The expression clearly exceeded that of a known functional V gene, A2, indicating that functional A18 alleles contribute significantly to the available antibody repertoire. In this context, it is surprising that the functional A18b allele apparently has been negatively selected in the Caucasian population, among whom 85% completely lack a functional gene.

AB - Immunoglobulin gene polymorphisms are interesting because they reflect differences in the available antibody repertoire which may affect the susceptibility to specific infections. Until recently, the human V kappa gene, A18, was known as a nonfunctional gene only. In this study, we cloned and sequenced four apparently functional alleles and determined the gene frequencies in three well-defined populations: Danish Caucasians, eastern Greenland Eskimos and Mozambican blacks. The A18b allele that was recently described in Native American Navajos by Atkinson et al. was found in all three populations with gene frequencies of 8%, 45% and 23% in Caucasians, Eskimos and blacks, respectively. Conversely, the frequencies of the nonfunctional A18a allele were 92%, 55% and 57%. Further, three new A18 alleles, c, d, and e were found exclusively in blacks, among whom they had an total frequency of 19%. These data indicate that both the A18a and A18b alleles originated before the diversification of Africans and non-Africans 90,000 years ago, whereas the A18c, A18d and A18e alleles may have a more recent origin. The functionality of the A18b allele was documented by the demonstration of properly rearranged and somatically hypermutated A18b messenger RNA present in the blood lymphocytes of individuals carrying this allele. The expression clearly exceeded that of a known functional V gene, A2, indicating that functional A18 alleles contribute significantly to the available antibody repertoire. In this context, it is surprising that the functional A18b allele apparently has been negatively selected in the Caucasian population, among whom 85% completely lack a functional gene.

KW - African Continental Ancestry Group/genetics

KW - Alleles

KW - Amino Acid Sequence

KW - Base Sequence

KW - Cloning, Molecular

KW - DNA, Complementary

KW - Denmark

KW - European Continental Ancestry Group/genetics

KW - Gene Expression

KW - Humans

KW - Immunoglobulin Variable Region/genetics

KW - Immunoglobulin kappa-Chains/genetics

KW - Inuits/genetics

KW - Molecular Sequence Data

KW - Mozambique

KW - Polymerase Chain Reaction

KW - Polymorphism, Genetic

KW - Polymorphism, Restriction Fragment Length

KW - RNA, Messenger

M3 - Journal article

C2 - 9234481

VL - 49

SP - 595

EP - 604

JO - HLA

JF - HLA

SN - 2059-2302

IS - 6

ER -

ID: 202982073