Literature DB >> 8093607

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

W J Zhang1, F T Christiansen, X Wu, L J Abraham, M Giphart, R L Dawkins.   

Abstract

The evolutionary relationship between two central major histocompatibility complex (MHC) genes, C4 and CYP21, was investigated by employing pulsed field gel electrophoresis (PFGE) and conventional restriction fragment length polymorphism (RFLP) analyses in human and nonhuman primates. Using Taq I in conjunction with C4 and CYP21 probes, it has been found that there are four major types of C4 genes [defined by 7.0, 6.4, 6.0, and 5.4 kilobases (kb) Taq I fragments] and two major types of CYP21 genes (3.7 and 3.2 kb fragments) in human and nonhuman primates including chimpanzee, gorilla, and orangutan. All of the eight possible combinations of C4 and CYP21 genes can be identified on one or more human ancestral haplotypes (AH). It is concluded that each of the major types of C4 and CYP21 (and each of the combinations between these) predated human speciation. PFGE analysis with Mlu I and Pvu I suggested that each C4+CYP21 segment has a specific length of 30-50 kb and that each AH carries one, two, three, or even more segments. In the case of C4, it is important to note that there is no simple relationship between the RFLP and the protein classifications. Thus, at least some of the expressed polymorphisms could be relatively recent in that they are carried by the same or different gene types. These findings are consistent with the hypothesis that MHC AHs have been formed from a large pool of specific genomic segments and that further haplospecific polymorphism has developed subsequently.

Entities:  

Mesh:

Substances:

Year:  1993        PMID: 8093607     DOI: 10.1007/bf00191881

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


  32 in total

1.  C4 genes of the chimpanzee, gorilla, and orang-utan: evidence for extensive homogenization.

Authors:  H Kawaguchi; Z Zaleska-Rutczynska; F Figueroa; C O'hUigin; J Klein
Journal:  Immunogenetics       Date:  1992       Impact factor: 2.846

2.  Detection of specific sequences among DNA fragments separated by gel electrophoresis.

Authors:  E M Southern
Journal:  J Mol Biol       Date:  1975-11-05       Impact factor: 5.469

3.  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

4.  A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity.

Authors:  A P Feinberg; B Vogelstein
Journal:  Anal Biochem       Date:  1983-07-01       Impact factor: 3.365

5.  Polymorphism of the human complement C4 and steroid 21-hydroxylase genes. Restriction fragment length polymorphisms revealing structural deletions, homoduplications, and size variants.

Authors:  P M Schneider; M C Carroll; C A Alper; C Rittner; A S Whitehead; E J Yunis; H R Colten
Journal:  J Clin Invest       Date:  1986-09       Impact factor: 14.808

6.  Organization of the chimpanzee C4-CYP21 region: implications for the evolution of human genes.

Authors:  H Kawaguchi; M Golubic; F Figueroa; J Klein
Journal:  Eur J Immunol       Date:  1990-04       Impact factor: 5.532

7.  Two steroid 21-hydroxylase genes are located in the murine S region.

Authors:  P C White; D D Chaplin; J H Weis; B Dupont; M I New; J G Seidman
Journal:  Nature       Date:  1984 Nov 29-Dec 5       Impact factor: 49.962

8.  Multiple duplications of complement C4 gene correlate with H-2-controlled testosterone-independent expression of its sex-limited isoform, C4-Slp.

Authors:  M Levi-Strauss; M Tosi; M Steinmetz; J Klein; T Meo
Journal:  Proc Natl Acad Sci U S A       Date:  1985-03       Impact factor: 11.205

9.  Definitive RFLPs to distinguish between the human complement C4A/C4B isotypes and the major Rodgers/Chido determinants: application to the study of C4 null alleles.

Authors:  C Y Yu; R D Campbell
Journal:  Immunogenetics       Date:  1987       Impact factor: 2.846

10.  Extensive deletions and insertions in different MHC supratypes detected by pusled field gel electrophoresis.

Authors:  K Tokunaga; G Saueracker; P H Kay; F T Christiansen; R Anand; R L Dawkins
Journal:  J Exp Med       Date:  1988-09-01       Impact factor: 14.307

View more
  3 in total

1.  The major histocompatability complex (MHC) contains conserved polymorphic genomic sequences that are shuffled by recombination to form ethnic-specific haplotypes.

Authors:  S Gaudieri; C Leelayuwat; G K Tay; D C Townend; R L Dawkins
Journal:  J Mol Evol       Date:  1997-07       Impact factor: 2.395

2.  Complement component C4 gene intron 9 as a phylogenetic marker for primates: long terminal repeats of the endogenous retrovirus ERV-K(C4) are a molecular clock of evolution.

Authors:  A W Dangel; B J Baker; A R Mendoza; C Y Yu
Journal:  Immunogenetics       Date:  1995       Impact factor: 2.846

3.  C4 gene polymorphism in primates: evolution, generation, and Chido and Rodgers antigenicity.

Authors:  E Paz-Artal; A Corell; M Alvarez; P Varela; L Allende; A Madroño; M Rosal; A Arnaiz-Villena
Journal:  Immunogenetics       Date:  1994       Impact factor: 2.846

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.