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Structure and Macromolecular Composition of the Egg and Embryo Jelly Coats of the Anuran Lepidobatrachus laevis
Author(s) -
Carroll Edward J.,
Wei Susan H.,
Nagel Glenn M.,
Ruibal Rodolfo
Publication year - 1991
Publication title -
development, growth and differentiation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.864
H-Index - 66
eISSN - 1440-169X
pISSN - 0012-1592
DOI - 10.1111/j.1440-169x.1991.00037.x
Subject(s) - embryo , royal jelly , chemistry , biology , human fertilization , anatomy , biochemistry , botany , microbiology and biotechnology
Eggs and cleavage‐stage embryos of the frog Lepidobatrachus laevis are encased by 3 μm thick vitelline/fertilization envelope and two jelly layers, termed J 1 (innermost) and J 2 (outermost). Based on light and transmission electron microscopy, J 1 had a dense reticular appearance whereas J 2 had a laminar structure. Direct dissolution of the jelly coats was accomplished by reduction of disulfide bonds with 0.08 M 2‐mercaptoethanol at pH 10. Soluble jelly preparations were uncontaminated with nucleic acid (A 280 /A 260 =1.44) and yielded an average of 150 μg protein/egg or embryo (n=5). The biochemical composition of the jelly coats in unfertilized eggs was different from that in embryos. When examined via gel permeation chromatography, soluble jelly from unfertilized eggs contained macromolecules which were markedly larger and more heterogeneous (earlier eluting and broader peaks) than jelly from embryos. Differences in the components of jelly from unfertilized eggs and embryos were also observed by electrophoresis, however, a 29,700 molecular weight glycoprotein chain was common to both jelly preparations. The electrophoretic pattern of jelly obtained from parthenogenetically activated eggs was identical to that of unfertilized eggs, therefore the fertilization‐associated changes are not due to the exclusive action of cortical granule products.