Skip to main content
Log in

What Can Medicine Learn from the Human DNA Sequence?

  • Published:
Biochemistry (Moscow) Aims and scope Submit manuscript

Abstract

The cooperation of biochemistry with clinical medicine consists of two overlapping temporal phases. Phase 1 of the cooperation, which still is not finished, is characterized by joint work on the pathogenesis and diagnostics of systemic metabolic diseases, whereas in phase 2 the cooperation on tissue and cell specific as well as on molecular diseases is prevailing. In view of the conceptual revolution and shift in paradigm, which biochemistry and medicine are presently experiencing, the content of cooperation between the two disciplines will profoundly change. It will become deeply influenced by the results of the research into the human genome and human proteome. Biochemistry will strongly be occupied to relate the thousands of protein coding genes to the structure and function of the encoded proteins, and medicine will be concerned in finding new protein markers for diagnostics, to identify novel drug targets, and to investigate, for example, the proteomes of the variety of tumors to aid tumor classification, to mention only a few areas of interest which medicine will have in the progress of human genome research. The review summarizes the recent achievements in sequencing the human DNA as published in February 2001 by the International Human Genome Sequencing Consortium and Celera Genomics and discusses their significance in respect to the further development of molecular, in particular genetic, medicine as an interdisciplinary field of the modern clinical sciences. Only biochemistry can provide the conceptual and experimental basis for the causal understanding of biological mechanisms as encoded in the genome of an organism.

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.

Similar content being viewed by others

REFERENCES

  1. Brenner, S. (2000) Trends Biochem. Sci., 25, 584.

    Google Scholar 

  2. International Human Genome Sequencing Consortium: Initial Sequencing and Analysis of the Human Genome (2001) Nature, 409, 860–921.

  3. Venter, J. C., et al. (2001) Science, 291, 1304–1351.

    Google Scholar 

  4. Goffeau, A., et al. (1996) Science, 274, 546–567.

    Google Scholar 

  5. The C. elegans Sequencing Consortium: Genome Sequence of the Nematode C. elegans: A Platform for Investigating Biology (1998) Science, 282, 2012–2022.

  6. Adams, M. D., et al. (2000) Science, 287, 2185–2195.

    Google Scholar 

  7. The Arabidopsis Genome Initiative: Analysis of the Genome Sequence of the Flowering Plant Arabidopsis thaliana (2000) Nature, 408, 796–815.

  8. Bird, A. P. (1987) Trends Genet., 3, 342–347.

    Google Scholar 

  9. Ban, N., Nissen, P., Hansen, J., Moore, P. B., and Steitz, T. A. (2000) Science, 289, 905–920.

    Google Scholar 

  10. Nissen, P., Hansen, J., Ban, N., Moore, P. B., and Steitz, T. A. (2000) Science, 289, 920–930.

    Google Scholar 

  11. Orgel, L. E., and Crick, F. H. C. (1980) Nature, 284, 604–607.

    Google Scholar 

  12. Baltimore, D. (2001) Nature, 409, 814–816.

    Google Scholar 

  13. Okada, N., Hamada, M., Ogiwara, I., and Ohshima, K. (1997) Gene, 205, 229–243.

    Google Scholar 

  14. Esnault, C., Maestre, J., and Heidmann, T. (2000) Nature Genet., 24, 363–367.

    Google Scholar 

  15. Jurka, J., and Kapitonov, V. V. (1999) Genetica, 107, 239–248.

    Google Scholar 

  16. Bork, P., and Copley, R. (2001) Nature, 409, 818–820.

    Google Scholar 

  17. Chakravarti, A. (2001) Nature, 409, 822–823.

    Google Scholar 

  18. The International SNP Map Working Group (2001) Nature, 409, 928–933.

    Google Scholar 

  19. Abbott, A. (1999) Nature, 402, 715–720.

    Google Scholar 

  20. Gerlt, J. A., and Babitt, P. C. (2000) http://genomebiology. com/2000/I/5/reviews/0005.I

  21. Futreal, P. A., Kasprzyk, A., Birney, E., Mullikin, J. C., Wooster, R., and Stratton, M. R. (2001) Nature, 409, 850–852.

    Google Scholar 

  22. Jimenez-Sanchez, G., Childs, B., and Valle, D. (2001) Nature, 409, 853–855.

    Google Scholar 

  23. Fahrer, A. M., Bazan, J. F., Papathanasiou, P., Nelms, K. A., and Goodnow, C. (2001) Nature, 409, 836–838.

    Google Scholar 

  24. Pollard, T. D. (2001) Nature, 409, 842–843.

    Google Scholar 

  25. Bock, J. B., Matern, H. T., Peden, A. A., and Scheller, R. H. (2001) Nature, 409, 839–841.

    Google Scholar 

  26. Nestler, E. J., and Landsman, D. (2001) Nature, 409, 834–835.

    Google Scholar 

  27. Tupler, R., Perini, G., and Green, M. R. (2001) Nature, 409, 832–833.

    Google Scholar 

  28. Chen, F. W., and Ioannou, Y. A. (1999) Int. Rev. Immunol., 18, 429–448.

    Google Scholar 

  29. Madsen, H. O., Poulsen, K., Dahl, O., Clark, B. F., and Hjorth, J. P. (1990) Nucleic Acids Res., 18, 1513–1516.

    Google Scholar 

  30. Meyer-Siegler, K., et al. (1991) Proc. Natl. Acad. Sci. USA, 88, 8460–8464.

    Google Scholar 

  31. Mansur, N. R., Meyer-Siegler, K., Wurzer, J. C., and Sirover, M. A. (1993) Nucleic Acids Res., 21, 993–998.

    Google Scholar 

  32. Tatton, N. A. (2000) Exp. Neurol., 166, 29–43.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Hofmann, E. What Can Medicine Learn from the Human DNA Sequence?. Biochemistry (Moscow) 66, 1144–1152 (2001). https://doi.org/10.1023/A:1012437114597

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1012437114597

Navigation