Literature DB >> 3036685

Gene organization of haplotypes expressing two different C4A allotypes.

A Palsdottir, A Arnason, R Fossdal, O Jensson.   

Abstract

The gene organization of C4 haplotypes expressing two different C4A allotypes with a C4B null allele (C4A3A2BQ0 and C4A3A6BQO) was studied using Southern blot analysis with cDNA probes and restriction enzymes which give C4A and C4B locus-specific restriction fragments. These haplotypes were shown to have both a C4A and a C4B locus present, suggesting that the C4B locus expresses a C4A protein. The finding of a 21-OH A and a 21-OH B gene on the C4A3A6BQO haplotype further suggests that this haplotype has the common gene organization C4A, 21-OH A, C4B, 21-OH B. A model explaining C4 null alleles on haplotypes found to have two C4 loci is presented.

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Year:  1987        PMID: 3036685     DOI: 10.1007/BF00283611

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  29 in total

1.  Report of the Committee on the Genetic Constitution of Chromosomes 5 and 6.

Authors:  L U Lamm; B Olaisen
Journal:  Cytogenet Cell Genet       Date:  1985

2.  Heterogeneity of human C4 gene size. A large intron (6.5 kb) is present in all C4A genes and some C4B genes.

Authors:  A Palsdottir; R Fossdal; A Arnason; J H Edwards; O Jensson
Journal:  Immunogenetics       Date:  1987       Impact factor: 2.846

3.  Genetics of human C4 polymorphism: detection and segregation of rare and duplicated haplotypes.

Authors:  C Rittner; C M Giles; M H Roos; P Démant; E Mollenhauer
Journal:  Immunogenetics       Date:  1984       Impact factor: 2.846

4.  Polymorphic DNA region adjacent to the 5' end of the human insulin gene.

Authors:  G I Bell; J H Karam; W J Rutter
Journal:  Proc Natl Acad Sci U S A       Date:  1981-09       Impact factor: 11.205

5.  The structure of a mutant H-2 gene suggests that the generation of polymorphism in H-2 genes may occur by gene conversion-like events.

Authors:  E H Weiss; A Mellor; L Golden; K Fahrner; E Simpson; J Hurst; R A Flavell
Journal:  Nature       Date:  1983-02-24       Impact factor: 49.962

6.  C4 haplotypes with duplications at the C4A or C4B loci: frequency and associations with BF, C2, and HLA-A, B, C, DR alleles.

Authors:  B Uring-Lambert; J Goetz; M M Tongio; S Mayer; G Hauptmann
Journal:  Tissue Antigens       Date:  1984-07

7.  C4 and HLA haplotypes associated with partial inhibition of anti-Rg and anti-Ch.

Authors:  C M Giles; J R Batchelor; I A Dodi; A H Fielder; C Rittner; G Mauff; K Bender; C Levene; G M Schreuder; L J Wells
Journal:  J Immunogenet       Date:  1984 Oct-Dec

8.  MHC-linked class III genes. Analysis of C4 gene frequencies, complotypes and associations with distinct HLA haplotypes in German Caucasians.

Authors:  D J Schendel; G J O'Neill; R Wank
Journal:  Immunogenetics       Date:  1984       Impact factor: 2.846

9.  Mapping of steroid 21-hydroxylase genes adjacent to complement component C4 genes in HLA, the major histocompatibility complex in man.

Authors:  M C Carroll; R D Campbell; R R Porter
Journal:  Proc Natl Acad Sci U S A       Date:  1985-01       Impact factor: 11.205

10.  Family study of the major histocompatibility complex in patients with systemic lupus erythematosus: importance of null alleles of C4A and C4B in determining disease susceptibility.

Authors:  A H Fielder; M J Walport; J R Batchelor; R I Rynes; C M Black; I A Dodi; G R Hughes
Journal:  Br Med J (Clin Res Ed)       Date:  1983-02-05
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  11 in total

1.  Complement 4 phenotypes and genotypes in Brazilian patients with classical 21-hydroxylase deficiency.

Authors:  G Guerra-Junior; A Sevciovic Grumach; S H Valente de Lemos-Marini; M Kirschfink; A Condino Neto; M de Araujo; M Palandi De Mello
Journal:  Clin Exp Immunol       Date:  2009-02       Impact factor: 4.330

2.  Restriction fragment analysis of non-deleted complement C4 null genes suggests point mutations in C4A null alleles, but gene conversions in C4B null alleles.

Authors:  J Partanen; R D Campbell
Journal:  Immunogenetics       Date:  1989       Impact factor: 2.846

3.  Rearrangements and point mutations of P450c21 genes are distinguished by five restriction endonuclease haplotypes identified by a new probing strategy in 57 families with congenital adrenal hyperplasia.

Authors:  Y Morel; J André; B Uring-Lambert; G Hauptmann; H Bétuel; M Tossi; M G Forest; M David; J Bertrand; W L Miller
Journal:  J Clin Invest       Date:  1989-02       Impact factor: 14.808

4.  Quantitative variation of C4 variant proteins associated with many MHC haplotypes.

Authors:  L Truedsson; Z Awdeh; E J Yunis; S Mrose; B Moore; C A Alper
Journal:  Immunogenetics       Date:  1989       Impact factor: 2.846

5.  Antigenic determinants expressed by human C4 allotypes; a study of 325 families provides evidence for the structural antigenic model.

Authors:  C M Giles; B Uring-Lambert; J Goetz; G Hauptmann; A H Fielder; W Ollier; C Rittner; T Robson
Journal:  Immunogenetics       Date:  1988       Impact factor: 2.846

Review 6.  Gene conversions, deletions, and polymorphisms in congenital adrenal hyperplasia.

Authors:  W L Miller
Journal:  Am J Hum Genet       Date:  1988-01       Impact factor: 11.025

7.  The study of a French family with two duplicated C4A haplotypes.

Authors:  C M Giles; B Uring-Lambert; W Boksch; M Braun; J Goetz; R Neumann; G Mauff; G Hauptmann
Journal:  Hum Genet       Date:  1987-12       Impact factor: 4.132

8.  Heterogeneity of human C4 gene size. A large intron (6.5 kb) is present in all C4A genes and some C4B genes.

Authors:  A Palsdottir; R Fossdal; A Arnason; J H Edwards; O Jensson
Journal:  Immunogenetics       Date:  1987       Impact factor: 2.846

9.  Possible association of sudden infant death with partial complement C4 deficiency revealed by post-mortem DNA typing of HLA class II and III genes.

Authors:  P M Schneider; C Wendler; T Riepert; L Braun; U Schacker; M Horn; H Althoff; R Mattern; C Rittner
Journal:  Eur J Pediatr       Date:  1989-12       Impact factor: 3.183

10.  Deficiencies of human complement component C4A and C4B and heterozygosity in length variants of RP-C4-CYP21-TNX (RCCX) modules in caucasians. The load of RCCX genetic diversity on major histocompatibility complex-associated disease.

Authors:  C A Blanchong; B Zhou; K L Rupert; E K Chung; K N Jones; J F Sotos; W B Zipf; R M Rennebohm; C Yung Yu
Journal:  J Exp Med       Date:  2000-06-19       Impact factor: 14.307

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