Literature DB >> 6149579

The factor B and C2 genes.

R D Campbell, D R Bentley, B J Morley.   

Abstract

Factor B and C2, components of the complement system, are novel types of serine proteinase that are encoded by genes in the major histocompatibility complex. cDNA probes specific for these two proteins have been used to isolate cosmid clones of genomic DNA which contain the Factor B and C2 genes. Southern blot analysis of the cosmid clones and of uncloned genomic DNA has shown that there are single Factor B and C2 loci that are less than 1 kilobase apart. The Factor B gene has been further characterized by DNA sequence analysis. It is approximately 6 kilobases in length, and is split into 18 exons. The amino acid sequence of the Ba fragment contains three homologous regions which are encoded by separate exons, suggesting that they arose by DNA duplication events. In the serine proteinase domain each of the functionally important parts of the active site are encoded on separate exons. Comparison of this region of the gene with the exon organization of other serine proteinases shows a close correlation between them, but also reveals the presence of an exon in Factor B with no homologous counterpart in the other serine proteinases. The possible functional significance of the peptide encoded by this exon and the evolution of this novel serine proteinase are discussed.

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Year:  1984        PMID: 6149579     DOI: 10.1098/rstb.1984.0097

Source DB:  PubMed          Journal:  Philos Trans R Soc Lond B Biol Sci        ISSN: 0962-8436            Impact factor:   6.237


  13 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.  DNA polymorphism of the C2 locus.

Authors:  D R Bentley; R D Campbell; S J Cross
Journal:  Immunogenetics       Date:  1985       Impact factor: 2.846

3.  Normal polymorphic variations and transcription of the decay accelerating factor gene in paroxysmal nocturnal hemoglobinuria cells.

Authors:  H A Stafford; M L Tykocinski; D M Lublin; V M Holers; W F Rosse; J P Atkinson; M E Medof
Journal:  Proc Natl Acad Sci U S A       Date:  1988-02       Impact factor: 11.205

4.  A putative functional domain of human placental alkaline phosphatase predicted from sequence comparisons.

Authors:  P A Tsonis; W S Argraves; J L Millán
Journal:  Biochem J       Date:  1988-09-01       Impact factor: 3.857

Review 5.  Application of molecular cloning to studies on the complement system.

Authors:  K B Reid
Journal:  Immunology       Date:  1985-06       Impact factor: 7.397

6.  Molecular cloning and characterization of the cDNA coding for C4b-binding protein, a regulatory protein of the classical pathway of the human complement system.

Authors:  L P Chung; D R Bentley; K B Reid
Journal:  Biochem J       Date:  1985-08-15       Impact factor: 3.857

7.  Gene deletions correlate with the development of alloantibodies in von Willebrand disease.

Authors:  B B Shelton-Inloes; F F Chehab; P M Mannucci; A B Federici; J E Sadler
Journal:  J Clin Invest       Date:  1987-05       Impact factor: 14.808

8.  DNA polymorphism of the C2 and factor B genes. Detection of a restriction fragment length polymorphism which subdivides haplotypes carrying the C2C and factor B F alleles.

Authors:  S J Cross; J H Edwards; D R Bentley; R D Campbell
Journal:  Immunogenetics       Date:  1985       Impact factor: 2.846

9.  Production and functional activity of a recombinant von Willebrand factor-A domain from human complement factor B.

Authors:  S C Williams; J Hinshelwood; S J Perkins; R B Sim
Journal:  Biochem J       Date:  1999-09-15       Impact factor: 3.857

10.  Murine protein H is comprised of 20 repeating units, 61 amino acids in length.

Authors:  T Kristensen; B F Tack
Journal:  Proc Natl Acad Sci U S A       Date:  1986-06       Impact factor: 11.205

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