TY - JOUR
T1 - A test for masked message
T2 - The template activity of messenger ribonucleoprotein particles isolated from sea urchin eggs
AU - Jenkins, Nancy A.
AU - Kaumeyer, John F.
AU - Young, Elihu M.
AU - Raff, Rudolf A.
N1 - Funding Information:
We thank Dr. D. E. Leister for helpful discussions and Mrs. C. J. Huffman for skillful technical assistance. We also thank Dr. H. R. Mahler for a gift of pactamycin and General Mills, Inc., for its generous gift of the wheat germ used in this study. This work was supported by U.S.P.H.S. Grant HD 06902. R.A.R. is the recipient of U.S.P.H.S. Career Development Award K04 HD47. J.F.K. is a predoctoral trainee in Genetics supported by N.I.H. Training Grant 82. N.A.J. and E.M.Y. are predoctoral trainees in Molecular and Cell Biology supported by U.S.P.H.S. Award T32 GM 07227.
Copyright:
Copyright 2014 Elsevier B.V., All rights reserved.
PY - 1978/4
Y1 - 1978/4
N2 - The hypothesis that the "masked message" of unfertilized eggs consists of nontranslatable mRNP particles was directly tested by in vitro translation of mRNPs in a system derived from wheat germ. Three classes of mRNPs were tested: particles prepared from sea urchin eggs in buffers containing 0.35 M K+, particles prepared from sea urchin eggs in 0.35 M Na+, and particles released with EDTA in 0.35 M K+ from polysomes of sea urchin embryos cultured in the presence of actinomycin D. The mRNA content of particles was monitored by determination of poly(A) content. The wheat germ system used is quantitatively stimulated by addition of mRNA derived from eggs or from any of the classes of mRNPs used. Particles prepared from eggs with Na+ or released from polysomes contain less protein than particles isolated from eggs in K+, and as expected these particles are fully translatable in vitro. Particles prepared from eggs in buffers containing 0.35 M K+ produce little or no stimulation in the in vitro system. That this lack of translation represents in vivo masking is indicated by several considerations: (1) The nontranslatable particles were prepared in 0.35 M K+ and 5 mM Mg2+, ion concentrations similar to those found in echinoderm eggs; (2) density and sedimentation rate characteristics of the particles are little changed by isolation; (3) RNA extracted from isolated particles is fully translatable; and (4) particles prepared from polysomes or under conditions which destabilize RNPs are translatable. These data support the masking hypothesis for the protein synthesis repression system of eggs.
AB - The hypothesis that the "masked message" of unfertilized eggs consists of nontranslatable mRNP particles was directly tested by in vitro translation of mRNPs in a system derived from wheat germ. Three classes of mRNPs were tested: particles prepared from sea urchin eggs in buffers containing 0.35 M K+, particles prepared from sea urchin eggs in 0.35 M Na+, and particles released with EDTA in 0.35 M K+ from polysomes of sea urchin embryos cultured in the presence of actinomycin D. The mRNA content of particles was monitored by determination of poly(A) content. The wheat germ system used is quantitatively stimulated by addition of mRNA derived from eggs or from any of the classes of mRNPs used. Particles prepared from eggs with Na+ or released from polysomes contain less protein than particles isolated from eggs in K+, and as expected these particles are fully translatable in vitro. Particles prepared from eggs in buffers containing 0.35 M K+ produce little or no stimulation in the in vitro system. That this lack of translation represents in vivo masking is indicated by several considerations: (1) The nontranslatable particles were prepared in 0.35 M K+ and 5 mM Mg2+, ion concentrations similar to those found in echinoderm eggs; (2) density and sedimentation rate characteristics of the particles are little changed by isolation; (3) RNA extracted from isolated particles is fully translatable; and (4) particles prepared from polysomes or under conditions which destabilize RNPs are translatable. These data support the masking hypothesis for the protein synthesis repression system of eggs.
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U2 - 10.1016/0012-1606(78)90134-3
DO - 10.1016/0012-1606(78)90134-3
M3 - Article
C2 - 565309
AN - SCOPUS:0017806336
SN - 0012-1606
VL - 63
SP - 279
EP - 298
JO - Developmental Biology
JF - Developmental Biology
IS - 2
ER -