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LOCALIZATION OF DYNEIN IN SEA URCHIN EGGS DURING CLEAVAGE *
Author(s) -
MOHRI H.,
MOHRI TOSHIKO,
MABUCHI I.,
YAZAKI IKUKO,
SAKAI H.,
OGAWA K.
Publication year - 1976
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.1976.00391.x
Subject(s) - sea urchin , dynein , biology , anaphase , mitosis , cytokinesis , microbiology and biotechnology , cleavage furrow , microtubule , flagellum , antiserum , dynein atpase , metaphase , prophase , cleavage (geology) , cell division , meiosis , biochemistry , cell , genetics , cell cycle , antibody , chromosome , paleontology , fracture (geology) , gene
Detection and localization of dynein in cleaving sea urchin eggs were attempted using antidynein serum (prepared against a tryptic fragment of dynein, Fragment A, of sea urchin sperm flagella) and fluorescein conjugated goat antiserum to rabbit γ‐globulin. In both unfertilized and newly fertilized eggs, fluorescence was distributed rather uniformly within the cells but was absent from the nuclei. At prophase, intense fluorescence was observed on both sides of nucleus, suggesting accumulation of dynein in developing asters. From metaphase to anaphase, the whole mitotic apparatus (MA) was stained with the exceptions of the chromosomes and pole areas. Fluorescence then again became dispersed within the eggs. Throughout the mitotic process and cytokinesis, the egg cortex including the cleavage furrow was stained intensely, presumably reflecting the presence of dynein in this region. Similar distributions of fluorescence were obtained with the isolated MAs. Neither non‐immune serum nor the antiserum to which Fragment A was absorbed stained the eggs. Little staining was obtained with the antiserum against starfish egg myosin. The results, together with the finding that the chromosome motion in the isolated MAs was completely inhibited by anti‐dynein serum, but not with the anti‐myosin serum, suggest an active role played by a tubulin‐dynein system in mitosis.