Literature DB >> 2900212

Polymorphism of MHC class III genes: definition of restriction fragment linkage groups and evidence for frequent deletions and duplications.

N Ghanem1, B Uring-Lambert, M Abbal, G Hauptmann, M P Lefranc, G Lefranc.   

Abstract

The loci for the complement proteins BF and C2 and the two loci for C4 are closely linked to one another, as are the duplicated steroid 21 hydroxylase (21-OHase) genes to the C4A and C4B loci. The alleles of these four loci occur in specific combinations termed "complotypes". We have studied the gene frequencies of their different products in the Lebanese population and compared these values with those found in other populations. We observed a novel complotype (S B 4 6) in one family and a complotype with a so far undescribed variant of the C4A locus. Using several restriction fragment length polymorphisms (RFLPs), we have defined restriction fragment linkage groups. The combined use of C4 and 21-OHase probes allowed us to detect different types of deletions and duplications at these loci in the Lebanese population.

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Year:  1988        PMID: 2900212     DOI: 10.1007/bf00366239

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


  54 in total

1.  Genetic studies in Saudi Arabia: red cell enzyme, haemoglobin and serum protein polymorphisms.

Authors:  H W Goedde; H G Benkmann; D P Agarwal; L Hirth; U Bienzle; M Dietrich; H H Hoppe; J Orlowski; E Kohne; E Kleihauer
Journal:  Am J Phys Anthropol       Date:  1979-02       Impact factor: 2.868

2.  HLA markers in six Lebanese religious subpopulations.

Authors:  J L Serre; G Lefranc; J Loiselet; A Jacquard
Journal:  Tissue Antigens       Date:  1979-09

3.  Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I.

Authors:  P W Rigby; M Dieckmann; C Rhodes; P Berg
Journal:  J Mol Biol       Date:  1977-06-15       Impact factor: 5.469

4.  Isolation of cDNA clones for human complement component C2.

Authors:  D R Bentley; R R Porter
Journal:  Proc Natl Acad Sci U S A       Date:  1984-02       Impact factor: 11.205

5.  Common and uncommon immunoglobulin haplotypes among Lebanese communities.

Authors:  G Lefranc; L Rivat; J L Serre; J M Lalouel; G Pison; J Loiselet; C Ropartz; G de Lange; E van Loghem
Journal:  Hum Genet       Date:  1978-03-17       Impact factor: 4.132

6.  Complement C4 allotypes in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: further evidence for different allelic variants at the 21-hydroxylase locus.

Authors:  G J O'Neill; B Dupont; M S Pollack; L S Levine; M I New
Journal:  Clin Immunol Immunopathol       Date:  1982-05

7.  Gene order and gene distances in the HLA region studied by the haplotype method.

Authors:  B Olaisen; P Teisberg; R Jonassen; E Thorsby; T Gedde-Dahl
Journal:  Ann Hum Genet       Date:  1983-10       Impact factor: 1.670

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.  Two subtypes of BfF by isoelectrofocusing: differential linkage to other HLA markers.

Authors:  M Abbal; M Thomsen; A Cambon-Thomsen; J Archambeau; M Calot; D Fathallah
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

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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  4 in total

1.  Allelic associations of multiple RFLPs of the gene encoding complement protein C2.

Authors:  Z B Zhu; J E Volanakis
Journal:  Am J Hum Genet       Date:  1990-05       Impact factor: 11.025

2.  Defective, deleted or converted CYP21B gene and negative association with a rare restriction fragment length polymorphism allele of the factor B gene in congenital adrenal hyperplasia.

Authors:  N Ghanem; J M Lobaccaro; C Buresi; M Abbal; G Halaby; C Sultan; G Lefranc
Journal:  Hum Genet       Date:  1990-12       Impact factor: 4.132

3.  Extensive copy-number variation of young genes across stickleback populations.

Authors:  Frédéric J J Chain; Philine G D Feulner; Mahesh Panchal; Christophe Eizaguirre; Irene E Samonte; Martin Kalbe; Tobias L Lenz; Monika Stoll; Erich Bornberg-Bauer; Manfred Milinski; Thorsten B H Reusch
Journal:  PLoS Genet       Date:  2014-12-04       Impact factor: 5.917

4.  Diversification of spatiotemporal expression and copy number variation of the echinoid hbox12/pmar1/micro1 multigene family.

Authors:  Vincenzo Cavalieri; Fabiana Geraci; Giovanni Spinelli
Journal:  PLoS One       Date:  2017-03-28       Impact factor: 3.240

  4 in total

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