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Gamma ray-induced loss of expression of HLA and glyoxalase I alleles in lymphoblastoid cells.

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Kavathas, P, Bach, F H, DeMars, R·1980·Proceedings of the National Academy of Sciences

Abstract

Gamma rays from a cesium source were used to generate human lymphoblastoid cell line variants that had lost expression of all major histocompatibility complex antigens coded for by a single haplotype. The cell line was heterozygous at the glyoxalase I locus and had the HLA haplotypes HLA-A1, B8, DRw3, and HLA-A2, B5, DRw1. We selected with anti-HLA-B8 antiserum in a population of cells that had been irradiated with 300 R. The incidence of B8-loss variants was 4.1 X 10(-5) on day 5 after irradiation. Analysis of variants showed that expressions of HLA and GLO alleles trans to B8 were retained. However, expression of additional cis-linked HLA and GLO gene products was lost in 12 of 17 variants. Variants that had lost expression of (i) HLA-B8, (ii) HLA-B8, A1, (iii) HLA-B8, A1, DRw3, or (iv) HLA-B8, A1, DRw3 and the cis-linked glyoxalase I allele were obtained. Karyotype analysis was performed on eight variants that had lost expression of two or more cis-linked alleles. Three variants had two normal appearing no. 6 chromosomes, four variants had a deletion that included the region coding for HLA genes on the short arm of one no. 6 chromosome, and one variant had an inversion or translocation involving the short arm of one no. 6.

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Metadata

Authors
Kavathas, P., Bach, F. H., & DeMars, R.
Venue
Proceedings of the National Academy of Sciences
Published
1980-07
Volume
77
Issue
7
Pages
4251-4255
ISSN
  • 0027-8424 (ISSN-L)
  • 1091-6490
OpenAlex
W2090230058
Cited by
252
References
0
FWCI
28.80
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Gamma ray-induced loss of expression of HLA and glyoxalase I alleles in lymphoblastoid cells. https://app.cochat.ai/papers/10.1073/pnas.77.7.4251
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Kavathas, P., Bach, F. H., & DeMars, R. (1980). Gamma ray-induced loss of expression of HLA and glyoxalase I alleles in lymphoblastoid cells. Proceedings of the National Academy of Sciences. https://doi.org/10.1073/pnas.77.7.4251

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