Cell Lineage Analysis in Xenopus Embryos (original) (raw)

Abstract

Cell lineage studies reveal what kinds of tissues descend from a single cell or specific region of an embryo. By defining precisely from which cells the various tissues and organs arise one can elucidate the mechanisms that control body organization, understand morphogenetic movements, and test the influence of exogenously applied gene products on these events. Because of easy accessibility, complete fate maps of the early cleavage stages of Xenopus have been published (14). However, fate maps only describe the developmental path taken by a cell under normal, intact embryo conditions. Such studies cannot describe the full developmental potential of a cell or the times or mechanisms by which its fate is determined. The fate expressed by a cell, that is, the different tissue types that descend from it, is usually influenced by a number of factors, which may include maternal determinant molecules, cell-cell interactions, growth factor signals, and position within a morphogen gradient. Cell lineage tracing in Xenopus, therefore, is an essential technique to test the fate of a cell as it develops under novel experimental conditions (5). Lineage tracing also is an important tool for labeling host tissues for use in tissue recombinant experiments. The ability to recognize the origin of embryonic tissues was critical for interpreting the pioneering experiments of embryonic inductions (6,7). These early studies used pigmentation differences between donor and host species, but modern lineage labeling is more long lasting and reliable and allows tissues to be recombined within the same species.

Similar content being viewed by others

References

  1. Dale, L. and Slack, J. M. W. (1987) Fate map of the 32-cell stage of Xenopus laevis. Development 100, 279–295.
    PubMed CAS Google Scholar
  2. Moody, S. A. (1987) Fates of the blastomeres of the 16-cell stage Xenopus embryo. Dev. Biol. 119, 560–578.
    Article PubMed CAS Google Scholar
  3. Moody, S. A. (1987) Fates of the blastomeres of the 32-cell stage Xenopus embryo. Dev. Biol. 122, 300–319.
    Article PubMed CAS Google Scholar
  4. Moody, S. A. and Kline, M. J. (1990) Segregation of fate during cleavage of frog (Xenopus laevis) blastomeres. Anat. Embryol. 182, 347–362.
    Article PubMed CAS Google Scholar
  5. Moody, S. A. (1999) Testing the cell fate commitment of single blastomeres in Xenopus laevis, in Advances in Molecular Biology: A Comparative Methods Approach to the Study of Oocytes and Embryos (Richter, J., ed.), Oxford University Press, Oxford, UK, pp. 355–381.
    Google Scholar
  6. Spemann, H. and Mangold, H. (1924) Induction of embryonic primordia by implantation of organizers from a different species, in Foundations of Experimental Embryology (Willier, B. H. and Oppenheimer, J. M., eds.), Hafner, New York, pp. 144–184.
    Google Scholar
  7. Nieuwkoop, P. D. (1973) The “organization center” of the amphibian embryo: Its origin, spatial organization and morphogenetic action. Adv. Morphogen. 10, 1–39.
    CAS Google Scholar
  8. Guthrie, S., Turin, L., and Warner, A. E. (1988) Patterns of junctional communication during development of the early amphibian embryo. Development 103, 769–783.
    PubMed CAS Google Scholar
  9. Weisblat, D. A., Sawyer, R. T., and Stent, G. S. (1978) Cell lineage analysis by intracellular injection of a tracer enzyme. Science 202, 1295–1298.
    Article PubMed CAS Google Scholar
  10. Jacobson, M. (1985) Clonal analysis and cell lineages of the vertebrate nervous system. Annu. Rev. Neurosci. 8, 71–102.
    Article PubMed CAS Google Scholar
  11. Stent, G. S. and Weisblat, D. A. (1985) Cell lineage in the development of invertebrate nervous systems. Annu. Rev. Neurosci. 8, 45–70.
    Article PubMed CAS Google Scholar
  12. Gimlich, R. L. and Braun, J. (1985) Improved fluorescent compounds for tracing cell lineage. Dev. Biol. 109, 509–514.
    Article PubMed CAS Google Scholar
  13. Vize, P. D., Melton, D. A., Hemmati-Brivanlou, A., and Harland, R. M. (1991) Assays for gene function in developing Xenopus embryos. Methods Cell Biol. 36, 367–387.
    Article PubMed CAS Google Scholar
  14. Chalfie, M., Tu, Y., Euskirchen, G., Ward, W. W., and Prasher, D. C. (1994) Green fluorescent protein as a marker for gene expression. Science 263, 802–805.
    Article PubMed CAS Google Scholar
  15. Etheridge, A. L. and Richter, S. M. A. (1978) Xenopus laevis: Rearing and Breeding the African Clawed Frog. Nasco, Ft. Atkinson, WI.
    Google Scholar
  16. Heasman, J., Holwill, S., and Wylie, C. C. (1991) Fertilization of cultured Xenopus oocytes and use in studies of maternally inherited molecules. Methods Cell Biol. 36, 213–230.
    Article PubMed CAS Google Scholar
  17. Vincent, J.-P. and Gerhart, J. C. (1987) Subcortical rotation in Xenopus eggs: An early step in embryonic axis specification. Dev. Biol. 123, 526–539.
    Article PubMed CAS Google Scholar
  18. Klein, S. L. (1987) The first cleavage furrow demarcates the dorsal-ventral axis in Xenopus embryos. Dev. Biol. 120, 299–304.
    Article PubMed CAS Google Scholar
  19. Masho, R. (1990) Close correlation between the first cleavage plane and the body axis in early Xenopus embryos. Dev. Growth Differ. 32, 57–64.
    Article Google Scholar
  20. Hainski, A. M. and Moody, S. A. (1992) Xenopus maternal RNAs from a dorsal animal blastomere induce a secondary axis in host embryos. Development 116, 347–355.
    PubMed CAS Google Scholar
  21. Peng, H. B. (1991) Appendix A: Solutions and protocols. Methods Cell Biol. 36, 657–662.
    Article PubMed CAS Google Scholar
  22. Nakamura, O. and Kishiyama, K. (1971) Prospective fates of blastomeres at the 32-cell stage of Xenopus laevis embryos. Proc. Japan Acad. 47, 407–412.
    Google Scholar
  23. Hirose, G. and Jacobson, M. (1979) Clonal organization of the central nervous system of the frog. I. Clones stemming from individual blastomeres of the 16-cell and earlier stages. Dev. Biol. 71, 191–202.
    Article PubMed CAS Google Scholar
  24. Jacobson, M. and Hirose, G. (1981) Clonal organization of the central nervous system of the frog. II. Clones stemming from individual blastomeres of the 32-and 64-cell stages. J. Neurosci. 1, 271–284.
    PubMed CAS Google Scholar
  25. Sullivan, S. A., Moore, K. B., and Moody, S. A. (1998) Early events in frog blastomere fate determination, in Cell Lineage and Fate Determination (Moody, S. A., ed.), Academic, New York, pp. 297–321.
    Google Scholar

Download references

Author information

Authors and Affiliations

  1. Department of Anatomy and Cell Biology, The George Washington University Medical Center, Washington, DC
    Sally A. Moody

Authors

  1. Sally A. Moody
    You can also search for this author inPubMed Google Scholar

Editor information

Editors and Affiliations

  1. Thomas Jefferson University, Philadelphia, PA
    Rocky S. Tuan
  2. University of Pennsylvania, Philadelphia, PA
    Cecilia W. Lo

Rights and permissions

© 2000 Humana Press Inc., Totowa, NJ

About this protocol

Cite this protocol

Moody, S.A. (2000). Cell Lineage Analysis in Xenopus Embryos. In: Walker, J.M., Tuan, R.S., Lo, C.W. (eds) Developmental Biology Protocols. Methods in Molecular Biology™, vol 135. Humana Press. https://doi.org/10.1385/1-59259-685-1:331

Download citation

Publish with us