Literature DB >> 1060128

Relationship between release of surface proteins and metabolic activation of sea urchin eggs at fertilization.

J D Johnson, D Epel.   

Abstract

Macromolecular components are released from sea urchin eggs when their metabolism is activated at fertilization or by incubation in ammonia. When the released material is dialyzed, concentrated, and added back to partially activated eggs the rate of protein synthesis is suppressed to the level of the unactivated egg. The surface proteins of the unfertilized eggs can be labeled with 125I by a lactoperoxidase procedure. When fertilized or activated with various parthenogenetic agents, 15-25% of the total labeled protein is released; most of the label is associated with a 150,000-dalton glycoprotein. The extent of metabolic activation, as assessed by measuring increased protein synthesis, is correlated with the amount of surface label released. Several other proteins are released during activation but are not labeled by the lactoperoxidase procedure in the intact cell. We have not yet identified which of these components is responsible for suppressing protein synthesis, nor do we know if any of the other metabolic changes of fertilization such as K+ conductance and DNA synthesis are also suppressed. We suggest that these released components are surface molecules involved in maintaining the low metabolic state occurring at the end of oogenesis and that removal of these components during fertilization results in the release of the suppression of the egg.

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Year:  1975        PMID: 1060128      PMCID: PMC388744          DOI: 10.1073/pnas.72.11.4474

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  19 in total

1.  An analysis of the partial metabolic derepression of sea urchin eggs by ammonia: the existence of independent pathways.

Authors:  D Epel; R Steinhardt; T Humphreys; D Mazia
Journal:  Dev Biol       Date:  1974-10       Impact factor: 3.582

Review 2.  Membrane receptors.

Authors:  P Cuatrecasas
Journal:  Annu Rev Biochem       Date:  1974       Impact factor: 23.643

3.  Periodic change in the content of adenosine 3'5'-cyclic monophosphate with close relation to the cycle of cleavage in the sea urchin egg.

Authors:  I Yasumasu; A Fujiwara; K Ishida
Journal:  Biochem Biophys Res Commun       Date:  1973-09-18       Impact factor: 3.575

4.  Cleavage inhibition in marine eggs by puromycin and 6-dimethylaminopurine.

Authors:  L I Rebhun; D White; G Sander; N Ivy
Journal:  Exp Cell Res       Date:  1973-03-15       Impact factor: 3.905

5.  Protein kinase in the sea urchin egg cortices. Its purification and characterization and some properties of an endogenous protein kinase in the cortices.

Authors:  H Murofushi
Journal:  Biochim Biophys Acta       Date:  1974-10-17

6.  Reversible inhibition of protein synthesis in HeLa.

Authors:  G Koch
Journal:  Biochem Biophys Res Commun       Date:  1974-11-27       Impact factor: 3.575

Review 7.  Glycoproteins.

Authors:  R G Spiro
Journal:  Adv Protein Chem       Date:  1973

8.  Isolation of a major cell surface glycoprotein from fibroblasts.

Authors:  K M Yamada; J A Weston
Journal:  Proc Natl Acad Sci U S A       Date:  1974-09       Impact factor: 11.205

9.  On the synthesis of glutamine before and after fertilization of the sea urchin, Strongylocentrotus purpuratus.

Authors:  R Hartmann; B M Shapiro
Journal:  Exp Cell Res       Date:  1974-10       Impact factor: 3.905

10.  Activation of sea-urchin eggs by a calcium ionophore.

Authors:  R A Steinhardt; D Epel
Journal:  Proc Natl Acad Sci U S A       Date:  1974-05       Impact factor: 11.205

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  6 in total

1.  Turning on of activities in unfertilized sea urchin eggs: correlation with changes of the surface.

Authors:  D Mazia; G Schatten; R Steinhardt
Journal:  Proc Natl Acad Sci U S A       Date:  1975-11       Impact factor: 11.205

2.  The problem of sea urchin egg fertilization and its implications for biological studies.

Authors:  R Lallier
Journal:  Experientia       Date:  1977-10-15

3.  Enhancement of ionic currents through voltage-gated channels in the mouse oocyte after fertilization.

Authors:  N Yamashita
Journal:  J Physiol       Date:  1982-08       Impact factor: 5.182

4.  Changes in holding and ion-channel currents during activation of an ascidian egg under voltage clamp.

Authors:  M Kozuka; K Takahashi
Journal:  J Physiol       Date:  1982-02       Impact factor: 5.182

5.  Cytasters from sea urchin eggs parthenogenetically activated by procaine.

Authors:  G W Moy; B Brandriff; V D Vacquier
Journal:  J Cell Biol       Date:  1977-06       Impact factor: 10.539

6.  Isolation and characterization of the vitelline layer of sea urchin eggs.

Authors:  C G Glabe; V D Vacquier
Journal:  J Cell Biol       Date:  1977-11       Impact factor: 10.539

  6 in total

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