Literature DB >> 2888726

DNA polymorphism of human HLA-linked complement C4 allotypes, including C4 null alleles, in the Finnish population.

J Partanen1, L Peltonen, S Koskimies, M C Carroll.   

Abstract

Human HLA-linked complement C4 gene products, C4A and C4B, show extensive genetic polymorphism. In both loci, an allele without a gene product, C4 null, is also observed. We have performed a restriction enzyme analysis of genomic DNA samples from individuals having all common (frequency over 1%) C4 protein allotypes observed in the Finnish population. Only one allotype-specific RFLP marker was observed. With some enzymes a DNA polymorphism was observed, which was not detectable by C4 protein typing. Analysis of 10 different C4B null haplotypes and 4 C4A null haplotypes suggested that only one haplotype, HLA-B8 C4A0 B1, carried a C4A gene deletion. This was observed in all 4 unrelated individuals homozygous for this haplotype.

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Year:  1987        PMID: 2888726     DOI: 10.1159/000153711

Source DB:  PubMed          Journal:  Hum Hered        ISSN: 0001-5652            Impact factor:   0.444


  5 in total

1.  Counterregulatory effects of interferon-gamma and endotoxin on expression of the human C4 genes.

Authors:  J Kulics; H R Colten; D H Perlmutter
Journal:  J Clin Invest       Date:  1990-03       Impact factor: 14.808

2.  C4 null phenotypes among lupus erythematosus patients are predominantly the result of deletions covering C4 and closely linked 21-hydroxylase A genes.

Authors:  J Partanen; S Koskimies; E Johansson
Journal:  J Med Genet       Date:  1988-06       Impact factor: 6.318

3.  Heat shock protein 70 (HSP70) and complement C4 genotypes in patients with hyperthyroid Graves' disease.

Authors:  S Ratanachaiyavong; A G Demaine; R D Campbell; A M McGregor
Journal:  Clin Exp Immunol       Date:  1991-04       Impact factor: 4.330

4.  C4A gene deletion and HLA associations in black Americans with systemic lupus erythematosus.

Authors:  M L Olsen; R Goldstein; F C Arnett; M Duvic; M Pollack; J D Reveille
Journal:  Immunogenetics       Date:  1989       Impact factor: 2.846

5.  DNA polymorphism unique for a complotype with deletion of HLA-linked C4B and 21-hydroxylase B genes causing congenital adrenal hyperplasia.

Authors:  J Partanen; S Koskimies; I Sipilä
Journal:  Hum Genet       Date:  1988-04       Impact factor: 4.132

  5 in total

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