Skip to main content
Log in

Gene expression in chick morula

  • Short Communications
  • Published:
Roux's archives of developmental biology Aims and scope Submit manuscript

Summary

The polypeptides synthesized during the morula stage in the chick embryo are insensitive to transcriptional inhibition by α-amanitin. Protein synthesis seems to depend predominantely, if not exclusively, on the recruitment of maternal mRNA, rather than on embryonic gene expression in chick morula. The morula embryo expresses the heatshock polypeptides when stressed at 43°C. The heat-induced polypeptides are isoforms of polypeptides that are synthesized normally. These polypeptides are α-amanitin sensitive and appear to mark the first major expression of the embryonic genome in the chick embryo.

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.

References

  • Bolton VN, Oades PJ, Johnson MH (1984) The relationship between cleavage, DNA replication, and gene expression in the mouse 2-cell embryo. J Embryol Exp Morphol 79:139–163

    Google Scholar 

  • Davidson EH (1986) Gene activity in early development. Academic Press, New York

    Google Scholar 

  • Dura JM (1981) Stage dependent synthesis of heat shock induced proteins in early embryos of Drosophila melanogaster. Mol Gen Genet 184:381–385

    Google Scholar 

  • Edgar BA, Schubiger G (1986) Parameters controlling transcriptional activation during early Drosophila development. Cell 44:817–877

    Google Scholar 

  • Eyal-Giladi H, Kochav S (1976) From cleavage to primitive streak formation: a complementary normal table and a new look at the first stages of the development of the chick. I. General morphology. Dev Biol 49:321–337

    Google Scholar 

  • Graziosi G, Micali F, Marzari R, De Christini F, Savoini A (1980) Variability of response of early Drosophila embryo to heat shock. J Exp Zool 214:141–145

    Google Scholar 

  • Heikkila JJ, Schultz GA (1984) Different environmental stresses can activate the expression of a heat shock gene in rabbit blastocysts. Gamete Res 10:45–56

    Google Scholar 

  • Heikiila JJ, Kloc M, Bury J, Schultz GA, Browder LW (1985) Acquisition of the heat-shock response and thermotolerance during early development of Xenopus laevis. Dev Biol 107:483–489

    Google Scholar 

  • Hewlett S, Miller J, Schultz GA (1983) Induction of heat shock proteins in early embryos of Arbacia punctulata. Biol Bull 165:500

    Google Scholar 

  • Klog M, Heikkila JJ, Bury J, Browder LW (1983) Stage-dependent synthesis of heat shock protein and its relationship to thermotolerance in Xenopus laevis embryos. J Cell Biol 97:33a

    Google Scholar 

  • Laemmli UK (1970) Cleavage of structural proteins during assembly of the head bacteriophage T4. Nature 227:680–685

    Google Scholar 

  • Lindell TJ, Weinberg F, Morris PW, Roeder RG, Rutter WJ (1970) Specific inhibition of nuclear RNA polymerase II by α-amanitin. Science 170:447–149

    Google Scholar 

  • Morange M, Diu A, Bensaude O, Babinet C (1984) Altered expression of heat shock proteins in embryonal carcinoma and mouse early embryonic cells. Mol Cell Biol 4:730–735

    Google Scholar 

  • Newport J, Kirschner M (1982) A major developmental transition in early Xenopus embryos: II. Control of the onset of transcription. Cell 30:687–696

    Google Scholar 

  • Nickells RW, Browder LW (1985) Region-specific heat-shock protein synthesis correlates with a biphasic acquisition of thermotolerance in Xenopus laevis embryos. Dev Biol 112:391–395

    Google Scholar 

  • O'Farrell PH (1975) High resolution two-dimensional electrophoresis of proteins. J Biol Chem 250:4007–4021

    Google Scholar 

  • Roccheri MC, Di Bernardo MG, Giudice G (1981) Synthesis of heat shock proteins in developing sea urchins. Dev Biol 83:173–177

    Google Scholar 

  • Schlesinger MJ, Ashburner M, Tissieres A (1982) Heat shock: from bacteria to man. Cold Spring Harbor, New York

    Google Scholar 

  • Sekeris CE, Schmid W (1972) Action of α-amanitin in vivo and in vitro. FEBS Lett 27:41–5

    Google Scholar 

  • Wittig S, Hensse S, Keitel C, Elsner C, Wittig B (1983) Heat shock gene expression is regulated during teratocarcinoma cell differentiation and early embryonic development. Dev Biol 96:507–514

    Google Scholar 

  • Zagris N (1977) Translation of endogenous message in embryonic chick erythroid cell polysomes in a cell-free protein synthesizing system. Biochem Genet 15:825–832

    Google Scholar 

  • Zagris N, Eyal-Giladi H (1982) 5-Bromodeoxyuridine inhibition of the epiblast competence for primitive streak formation in the young chick blastoderm. Dev Biol 91:208–214

    Google Scholar 

  • Zagris N, Matthopoulos D (1985) Patterns of protein synthesis in the chick blastula: a comparison of the component areas of the epiblast and the primary hypoblast. Dev Genet 5:209–217

    Google Scholar 

  • Zagris N, Matthopoulos D (1986a) Differential heat shock gene expression in chick blastula. Roux's Arch Dev Biol 195:403–407

    Google Scholar 

  • Zagris N, Matthopoulos D (1986b) Induction of the primitive streak in the chick blastoderm embryo: patterns of protein synthesis. Roux's Arch Dev Biol 195:80–83

    Google Scholar 

  • Zagris N, Matthopoulos D (1987) Induction of gastrulation in chick embryo. Dev Genet 8:83–89

    Google Scholar 

  • Zylber EA, Penman S (1971) Products of RNA polymerases in HeLa cell nuclei. Proc Natl Acad Sci USA 68:2861–2865

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Zagris, N., Matthopoulos, D. Gene expression in chick morula. Roux's Arch Dev Biol 197, 298–301 (1988). https://doi.org/10.1007/BF00380024

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00380024

Key words

Navigation