Skip to main content
Log in

Genes for C4b-binding protein α- and β-chains (C4BPA andC4BPB) are located on chromosome 1, band 1q32, in humans and on chromosome 13 in rats

  • Brief Communication
  • Published:
Somatic Cell and Molecular Genetics

Abstract

C4b-binding protein is involved in the regulation of the complement system. It is a multimeric protein composed of seven identical α-chains and a single copy of a unique β-chain. The latter was identified only recently and its structure determined by cDNA cloning. Both subunits in C4b-binding protein belong to the same superfamily of proteins composed predominantly of tandemly arranged short consensus repeats (SCR) approximately 60 amino acid residues in length. The gene for the human α-chain is known to be located in a gene cluster on chromosome 1, band 1q32, which is called the regulators of complement activation (RCA) gene cluster. We have used cDNA probes for both α- and β-chains of human C4b-binding protein to localize their genes with an in situ hybridization technique. We find the genes for both chains to be located on chromosome 1, band 1q32, in the human. This suggests that the β-chain gene is also a member of the RCA gene cluster and that the α- and β-chain genes are located close to each other. The cDNA probes for the α- and β-chains also were used to screen mouse-rat somatic cell hybrids using Southern blotting to localize their genes in the rat. Both the α- and β-chain genes were shown to be located on chromosome 13 in the rat. These are the second and third genes to be located on rat chromosome 13, and the results suggest that the genes for the α- and the β-chains together with the gene for coagulation factor V represent a conserved chromosomal region in rat and man.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Literature cited

  1. Scharfstein, J., Ferreira, A., Gigli, I., and Nussenzweig, V. (1978).J. Exp. Med. 148207–222.

    Google Scholar 

  2. Fujita, T., Gigli, I., and Nussenzweig, V. (1978).J. Exp. Med. 1481044–1051.

    Google Scholar 

  3. Nagasawa, S., Ischihara, C., and Stroud, R.M., (1980).J. Immunol. 125578–582.

    Google Scholar 

  4. Law, S.K.A., and Reid, K.B.M. (1988).Complement (ed.) Male, D., (IRL Press, Oxford, U.K.).

    Google Scholar 

  5. Dahlbäck, B., and Stenflo, J. (1981).Proc. Natl. Acad. Sci. U.S.A. 782512–2516.

    Google Scholar 

  6. Dahlbäck, B. (1984).Sem. Thromb. Hemost. 2139–148.

    Google Scholar 

  7. Walker, F.J. (1981).J. Biol. Chem. 25611128–11131.

    Google Scholar 

  8. Walker, F.J. (1988).Sem. Thromb. Hemost. 14(2):216–221.

    Google Scholar 

  9. Walker, F.J., Chavin, S.I., and Fay, P.J. (1987).Arch. Biochem. Biophys. 252322–328.

    Google Scholar 

  10. Dahlbäck, B. (1983).Biochem. J. 209837–846.

    Google Scholar 

  11. Dahlbäck, B. (1983).Biochem. J. 209847–856.

    Google Scholar 

  12. Comp, P.C., Nixon, R.R., Cooper, M.R., and Esmon, C.T. (1984).J. Clin. Invest. 742082–2088.

    Google Scholar 

  13. Broekmans, A.W., Bertina, R.M., Reinalda-Poot, J., Engesser, L., Muller, H.P., Leeuw, J.A., Michiels, J.J., Brommer, E.J.P., and Briet, E. (1985).Thromb. Haemost. 53273–277.

    Google Scholar 

  14. Dahlbäck, B. (1986).J. Biol. Chem. 26112022–12027.

    Google Scholar 

  15. Hillarp, A., and Dahlbäck, B. (1988).J. Biol. Chem. 26312759–12764.

    Google Scholar 

  16. Dahlbäck, B., Smith, C.A., and Müller-Eberhard, H.J. (1983).Proc. Natl. Acad. Sci. U.S.A. 803461–3465.

    Google Scholar 

  17. Dahlbäck, B., and Müller-Eberhard, H.J. (1984).J. Biol. Chem. 25911631–11634.

    Google Scholar 

  18. Hillarp, A., Hessing, M., and Dahlbäck, B. (1989).FEBS Lett. 25953–56.

    Google Scholar 

  19. Chung, L.P., Bentley, D.R., and Reid, K.B.M. (1985).Biochem. J. 230133–141.

    Google Scholar 

  20. Hillarp, A., and Dahlbäck, B. (1990).Proc. Natl. Acad. Sci. U.S.A. 871183–1187.

    Google Scholar 

  21. Reid, K.B.M., Bentley, D.R., Campbell, R.D., Chung, L.P., Sim, R.B., Kristensen, T., and Tack, B.F. (1986).Immunol. Today 7230–234.

    Google Scholar 

  22. Janatova, J., Reid, K.M.B., and Willis, A.C. (1989).Biochemistry 284754–4761.

    Google Scholar 

  23. Rodriguez de Cordoba, S., Lublin, D., Rubinstein, P., and Atkinson, J.P. (1985).J. Exp. Med. 1611189–1195.

    Google Scholar 

  24. Rey-Campos, J., Rubinstein, P., and Rodriguez de Cordoba, S. (1987).J. Exp. Med. 166246–252.

    Google Scholar 

  25. Rey-Campos, J., Rubinstein, P., and Rodriguez de Cordoba, S. (1988).J. Exp. Med. 167664–669.

    Google Scholar 

  26. Carroll, M.C., Alicot, E.M., Katzman, P.J., Klickstein, L.B., Smith, J.A., and Fearon, D.T. (1988).J. Exp. Med. 1671271–1280.

    Google Scholar 

  27. Bora, N.S., Lublin, D.L., Kumar, B.V., Hockett, R.D., Holers, V.M., and Atkinson, J.P. (1989).J. Exp. Med. 169597–602.

    Google Scholar 

  28. Weiss, J.H., Morton, C.C. Bruns, G.A., Weiss, J.J., Klickstein, L.B., Wong, W.W., and Fearon, D.T. (1987).J. Immunol. 138312–319.

    Google Scholar 

  29. Lublin, D., Lemons, R.S., Le Beau, M.M., Holers, V.M., Tykocinski, M.L., Medof, M.E., and Atkinson, J.P. (1987).J. Exp. Med. 1651731–1736.

    Google Scholar 

  30. Seldin, M.F., Morse, H.C., III, Reeves, J.P., Schribner, C.L., LeBoeuf, R.C., and Steinberg, A.D. (1988).J. Exp. Med. 167688–693.

    Google Scholar 

  31. Barnum, S.R., Kristenson, T., Chaplin, D.D., Seldin, M.F., and Tack, B.F. (1989).Biochemistry 288312–8317.

    Google Scholar 

  32. Maniatis, T., Fritsch, E.F., and Sambrook, J. (1982).Molecular Cloning: A Laboratory Manual (Cold Spring Harbor Laboratory, Cold Spring Harbor, New York).

    Google Scholar 

  33. Zabel, B.U., Naylor, S.L., Sakaguchi, A.Y., Bell, G.I., and Shows, T.B. (1983).Proc. Natl. Acad. Sci. U.S.A. 806932–6936.

    Google Scholar 

  34. Islam, M.Q., and Levan, G. (1987).Hereditas 107127–130.

    Google Scholar 

  35. Buckle, V.J., and Craig, I.W. (1986). InHuman Genetics Disease: A Practical Approach (ed.), Davies, K.E., (IRL Press, Oxford), pp. 85–100.

    Google Scholar 

  36. Szpirer, J., Levan, G., Thorn, M., and Szpirer, C. (1984).Cytogenet. Cell Genet. 38142–149.

    Google Scholar 

  37. Dahlbäck, B., Hansson, C., Islam, Q., Szpirer, J., Szpirer, C., Lundwall, Å., and Levan, G. (1988).Somat. Cell Mol. Genet. 14509–514.

    Google Scholar 

  38. Blin, N., and Stafford, D.W. (1976).Nucleic Acids Res. 32303–2308.

    Google Scholar 

  39. Southern, E.M. (1975).J. Mol. Biol. 98503–518.

    Google Scholar 

  40. Feinberg, A.P., and Vogelstein, B. (1984).Anal. Biochem. 137266–267.

    Google Scholar 

  41. Hourcade, D., Holers, V.M., and Atkinson, J.P. (1989).Adv. Immunol. 45381–416.

    Google Scholar 

  42. Kristensen, T., Ogata, R.T., Chung, L.P., Reid, K.B.M., and Tack, B.F. (1987).Biochemistry 264668–4674.

    Google Scholar 

  43. Wang, H., Riddell, D.C., Guinto, E.R., MacGillivray, R.T.A., and Hamerton, J.L. (1988).Genomics 2324–328.

    Google Scholar 

  44. Szpirer, C., Szpirer, J., Islam, M.Q., and Levan, G. (1988).Curr. Top. Microbiol. Immunol. 13733–38.

    Google Scholar 

  45. Searle, A.G., Peters, J., Lyon, M.F., Hall, J.G., Evans, E.P., Edwards, J.H., and Buckle, V.J. (1989).Ann. Hum. Genet. 5389–140.

    Google Scholar 

  46. Kingsmore, S.F., Watson, M.L., Howard, T.A., and Seldin, M.F. (1989).Embo. J. 84073–4080.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Andersson, A., Dahlbäck, B., Hanson, C. et al. Genes for C4b-binding protein α- and β-chains (C4BPA andC4BPB) are located on chromosome 1, band 1q32, in humans and on chromosome 13 in rats. Somat Cell Mol Genet 16, 493–500 (1990). https://doi.org/10.1007/BF01233199

Download citation

  • Received:

  • Revised:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01233199

Keywords

Navigation