z-logo
Premium
Effects of Inhibitors of Myosin Light Chain Kinase and Other Protein Kinases on the First Cell Division of Sea Urchin Eggs
Author(s) -
Mabuchi Issei,
TakanoOhmuro Hiromi
Publication year - 1990
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.1990.00549.x
Subject(s) - sea urchin , myosin light chain kinase , kinase , microbiology and biotechnology , division (mathematics) , cell division , myosin , protein kinase a , rho associated protein kinase , chemistry , biology , biochemistry , cell , arithmetic , mathematics
We investigated effects of protein kinase inhibitors on the first cell division in sea urchin eggs on the assumption that phosphorylation of myosin is requisite for the formation and/or the contraction of the contractile ring. ML‐7 or ML‐9, which inhibits myosin light chain kinase (MLCK), inhibited cytokinesis with a half maximal inhibition at 0.1–0.2 mM. The nuclear division was accomplished normally at 0.2–0.25 mM where the cytokinesis was completely blocked. Fluorescent staining of actin filaments with rhodamine‐labeled phalloidin revealed that the contractile ring was not formed in the cleavage‐inhibited eggs. H‐7 which inhibits cAMP‐dependent protein kinase, cGMP‐dependent protein kinase and protein kinase C arrested the process of the division at mid‐cleavage at 0.25–0.3 mM and at metaphase or anaphase at 0.5 mM. H‐8 and HA1004, which inhibit cAMP‐dependent and cGMP‐dependent protein kinases did not show significant effect at millimolar order. In the presence of micromolar concentrations of staurosporine which preferentially inhibits protein kinase C and MLCK small mitotic apparatuses were formed, in which chromosomes did not form the metaphase plate. The role of phosphorylation in the cell division is discussed.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Empowering knowledge with every search