Literature DB >> 2883116

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

A Palsdottir, R Fossdal, A Arnason, J H Edwards, O Jensson.   

Abstract

In this article we present a study showing that the human C4 genes differ in length because of the presence or absence of a 6.5 kb intron near the 5' end of the gene. DNA from individuals of known HLA, factor B, and C4 haplotypes was analyzed for restriction fragment length polymorphism (RFLP) by Southern blot analysis with C4-specific cDNA probes. The RFLP patterns obtained showed that the C4 genes are either 22.5 kb or 16 kb in length. They are referred to as long and short C4 genes, respectively. A population study was carried out to examine the distribution of the gene size according to C4 allotypes and haplotypes. Long C4 genes included all C4A genes studied and also some C4B allotypes, e.g., B1 on most C4 A3B1 haplotypes. Similarly, C4B null genes were found to be of the long form. Other C4B allotypes tested were found to be coded for by short C4 genes, including B2, B1 in C4 A6B1 and C4 AQOB1 (with a single C4B gene haplotype).

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Year:  1987        PMID: 2883116     DOI: 10.1007/bf00404422

Source DB:  PubMed          Journal:  Immunogenetics        ISSN: 0093-7711            Impact factor:   2.846


  27 in total

1.  Gene organization of haplotypes expressing two different C4A allotypes.

Authors:  A Palsdottir; A Arnason; R Fossdal; O Jensson
Journal:  Hum Genet       Date:  1987-07       Impact factor: 4.132

Review 2.  Molecular genetics of the fourth component of human complement and steroid 21-hydroxylase.

Authors:  M C Carroll; K T Belt; A Palsdottir; Y Yu
Journal:  Immunol Rev       Date:  1985-10       Impact factor: 12.988

Review 3.  Molecular cloning and characterization of complementary and genomic DNA clones for mouse C4 and Slp.

Authors:  M Nonaka; K Nakayama; Y D Yeul; A Shimizu; M Takahashi
Journal:  Immunol Rev       Date:  1985-10       Impact factor: 12.988

4.  C4B gene polymorphism detected in a human cosmid clone.

Authors:  H L Prentice; P M Schneider; J L Strominger
Journal:  Immunogenetics       Date:  1986       Impact factor: 2.846

5.  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

6.  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

7.  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

8.  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

9.  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

10.  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

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  16 in total

1.  C4B gene polymorphisms among African and African-American HLA-Bw42-DRw18 haplotypes.

Authors:  P A Fraser; Z L Awdeh; P Ronco; S Simon; B Moore; D Fici; D Marcus-Bagley; E J Yunis; C A Alper
Journal:  Immunogenetics       Date:  1991       Impact factor: 2.846

2.  Gene organization of haplotypes expressing two different C4A allotypes.

Authors:  A Palsdottir; A Arnason; R Fossdal; O Jensson
Journal:  Hum Genet       Date:  1987-07       Impact factor: 4.132

3.  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

4.  Genesis by meiotic unequal crossover of a de novo deletion that contributes to steroid 21-hydroxylase deficiency.

Authors:  P Sinnott; S Collier; C Costigan; P A Dyer; R Harris; T Strachan
Journal:  Proc Natl Acad Sci U S A       Date:  1990-03       Impact factor: 11.205

5.  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

6.  Identification of a novel family of human endogenous retroviruses and characterization of one family member, HERV-K(C4), located in the complement C4 gene cluster.

Authors:  M Tassabehji; T Strachan; M Anderson; R D Campbell; S Collier; M Lako
Journal:  Nucleic Acids Res       Date:  1994-12-11       Impact factor: 16.971

7.  Organization and evolution of C4 and CYP21 genes in primates: importance of genomic segments.

Authors:  W J Zhang; F T Christiansen; X Wu; L J Abraham; M Giphart; R L Dawkins
Journal:  Immunogenetics       Date:  1993       Impact factor: 2.846

8.  CYP21/C4 gene organisation in Italian 21-hydroxylase deficiency families.

Authors:  P J Sinnott; C Livieri; M Sampietro; M Marconi; R Harris; F Severi; T Strachan
Journal:  Hum Genet       Date:  1992-03       Impact factor: 4.132

9.  Haplotypes of the steroid 21-hydroxylase gene region encoding mild steroid 21-hydroxylase deficiency.

Authors:  B Haglund-Stengler; E Martin Ritzén; J Gustafsson; H Luthman
Journal:  Proc Natl Acad Sci U S A       Date:  1991-10-01       Impact factor: 11.205

10.  Family studies of the steroid 21-hydroxylase and complement C4 genes define 11 haplotypes in classical congenital adrenal hyperplasia in The Netherlands.

Authors:  P F Koppens; T Hoogenboezem; D J Halley; C A Barendse; A J Oostenbrink; H J Degenhart
Journal:  Eur J Pediatr       Date:  1992-12       Impact factor: 3.183

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