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Sequence of cDNA encoding human insulin-like growth factor I precursor

Abstract

Somatomedins (SM) or insulin-like growth factors (IGF) constitute a heterogeneous group of peptides1 with important growth-promoting effects in vitro2,3 as well as in vivo4,5. Amino acid sequences have been determined for only two of them, IGF-I and IGF-II, which are highly homologous6,7. IGF-I, which is identical with SM-C8, is composed of 70 amino acid residues and IGF-II contains 73 amino acids and may be identical with SM-A9. Other peptides with different charge properties but with similar SM-like or insulin-like behaviour in biological and receptor assays, have been described but have not yet been fully characterized1. The liver is known to be a major site of production of these peptides10, but many other tissues—especially in the fetus11—may synthesize them as well. We report here the nucleotide sequence of a human liver cDNA encoding the complete amino acid sequence of IGF-I. The IGF-I coding region is flanked by sequences encoding an amino-terminal peptide of at least 25 amino acid residues and a carboxyl-terminal peptide of 35 amino acids. This provides evidence that IGF-I is synthesized as a precursor protein and that formation of IGF-I from this precursor requires proteolytic processing at both ends.

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References

  1. Van den Brande, J. L. & Hoogerbrugge, C. in Growth Hormone and Other Biologically Active Peptides (eds Pecile, A. & Müller, E. E.) 81–102 (Excerpta Medica, Amsterdam 1980).

    Google Scholar 

  2. Daughaday, W. H. Clin. endocr. Metab. 6, 117–135 (1977).

    Article  CAS  Google Scholar 

  3. Clemmons, D. R. & Van Wyk, J. J. J. cell. Phys. 106, 361–367 (1981).

    Article  CAS  Google Scholar 

  4. van Buul-Offers, S. & Van den Brande, J. L. in Growth Hormone and Other Biologically Active Peptides (eds Pecile, A. & Müller, E. E.) 103–122 (Excerpta Medica, Amsterdam 1980).

    Google Scholar 

  5. Schoenle, E. et al. Nature 296, 252–253 (1982).

    Article  ADS  CAS  PubMed  Google Scholar 

  6. Rinderknecht, E. & Humbel, R. E. FEBS Lett. 89, 283–286 (1978).

    Article  CAS  PubMed  Google Scholar 

  7. Rinderknecht, E. & Humbel, R. E. J. biol. Chem. 253, 2769–2775 (1978).

    CAS  PubMed  Google Scholar 

  8. Klapper, D. G., Svoboda, M. E. & Van Wyk, J. J. Endocrinology 112, 2215–2217 (1983).

    Article  CAS  PubMed  Google Scholar 

  9. Fryklund, L., Uthne, K. & Sievertsson, H. Biochem. biophys. Res. Commun. 61, 957–962 (1974).

    Article  CAS  PubMed  Google Scholar 

  10. Phillips, L. S. et al. Endocrinology 98, 606–614 (1976).

    Article  CAS  PubMed  Google Scholar 

  11. D'Ercole, A. J., Applewhite, G. T. & Underwood, L. E. Devl Biol. 75, 315–329 (1980).

    Article  CAS  Google Scholar 

  12. Woods, D. E. et al. Proc. natn. Acad. Sci. U.S.A. 79, 5661–5665 (1982).

    Article  ADS  CAS  Google Scholar 

  13. Talmadge, K., Stahl, S. & Gilbert, W. Proc. natn. Acad. Sci. U.S.A. 77, 3369–3373 (1980).

    Article  ADS  CAS  Google Scholar 

  14. Casadavan, M. & Cohen, S. N. J. molec. Biol. 138, 179–207 (1980).

    Article  Google Scholar 

  15. Breslow, J. L. et al. Proc. natn. Acad. Sci. U.S.A. 79, 6861–6865 (1982).

    Article  ADS  CAS  Google Scholar 

  16. Maxam, A. M. & Gilbert, W. Proc. natn. Acad. Sci. U.S.A. 74, 560–564 (1977).

    Article  ADS  CAS  Google Scholar 

  17. Maxam, A. M. & Gilbert, W. Meth. Enzym. 65, 499–560 (1980).

    Article  CAS  PubMed  Google Scholar 

  18. Hudson, P. et al. Nature 291, 127–131 (1981).

    Article  ADS  CAS  PubMed  Google Scholar 

  19. Hagenbüchle, O., Santer, M. & Steitz, J. A. Cell 13, 551–563 (1978).

    Article  PubMed  Google Scholar 

  20. Sargan, D. R., Gregory, S. P. & Butterworth, P. H. W. FEBS Lett. 147, 133–136 (1982).

    Article  CAS  PubMed  Google Scholar 

  21. Erni, B. & Stachelin, T. FEBS Lett. 148, 79–82 (1982).

    Article  CAS  PubMed  Google Scholar 

  22. Blobel, G. & Doberstein, B. J. Cell Biol. 67, 852–862 (1975).

    Article  CAS  PubMed  Google Scholar 

  23. Aquaviva, M. A. et al. Diabetes 31, 656–658 (1982).

    Article  Google Scholar 

  24. Vassilopoulou-Sellin, R. & Phillips, L. S. Endocrinology 110, 582–589 (1982).

    Article  CAS  PubMed  Google Scholar 

  25. Craig, R. K. et al. Nature 295, 345–347 (1982).

    Article  ADS  CAS  PubMed  Google Scholar 

  26. MacIntyre, I. et al. Nature 300, 460–462 (1982).

    Article  ADS  CAS  PubMed  Google Scholar 

  27. Bell, G. I. et al. Nature 282, 525–527 (1979).

    Article  ADS  CAS  PubMed  Google Scholar 

  28. Hudson, P. et al. Nature 301, 628–631 (1983).

    Article  ADS  CAS  PubMed  Google Scholar 

  29. Smith, D. R. & Calvo, T. M. Nucleic Acids Res. 8, 2255–2274 (1980).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

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Jansen, M., van Schaik, F., Ricker, A. et al. Sequence of cDNA encoding human insulin-like growth factor I precursor. Nature 306, 609–611 (1983). https://doi.org/10.1038/306609a0

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