TitleMaternal effect mutations of the sponge locus affect actin cytoskeletal rearrangements in Drosophila melanogaster embryos.
Publication TypeJournal Article
Year of Publication1992
AuthorsPostner, MA, Miller, KG, Wieschaus, EF
JournalJ Cell Biol
Volume119
Issue5
Pagination1205-18
Date Published1992 Dec
KeywordsActin Depolymerizing Factors, Animals, Cell Compartmentation, Cell Division, Cell Nucleus, Cytoskeleton, Destrin, Drosophila melanogaster, Extrachromosomal Inheritance, Fluorescent Antibody Technique, Genes, Insect, Microfilament Proteins, Morphogenesis, Video Recording
Abstract

In the syncytial blastoderm stage of Drosophila embryogenesis, dome-shaped actin "caps" are observed above the interphase nuclei. During mitosis, this actin rearranges to participate in the formation of pseudocleavage furrows, transient membranous invaginations between dividing nuclei. Embryos laid by homozygous sponge mothers lack these characteristic actin structures, but retain other actin associated structures and processes. Our results indicate that the sponge product is specifically required for the formation of actin caps and metaphase furrows. The specificity of the sponge phenotype permits dissection of both the process of actin cap formation and the functions of actin caps and metaphase furrows. Our data demonstrate that the distribution of actin binding protein 13D2 is unaffected in sponge embryos and suggest that 13D2 is upstream of actin in cortical cap assembly. Although actin caps and metaphase furrows have been implicated in maintaining the fidelity of nuclear division and the positions of nuclei within the cortex, our observations indicate that these structures are dispensible during the early syncytial blastoderm cell cycles. A later requirement for actin metaphase furrows in preventing the nucleation of mitotic spindles between inappropriate centrosomes is observed. Furthermore, the formation of actin caps and metaphase furrows is not a prerequisite for the formation of the hexagonal array of actin instrumental in the conversion of the syncytial embryo into a cellular blastoderm.

Alternate JournalJ. Cell Biol.