The Drosophila melanogaster YA protein is a maternally provided nuclear lamina component that is essential during the transition from meiosis to mitosis at the beginning of embryogenesis. Localization of YA to the nuclear envelope is required for its function; this localization is cell cycle- dependent during embryogenesis. Here we show that the ability of YA to enter nuclei is modulated during development. In developing egg chambers, YA protein is made but excluded from nuclei of nurse cells and oocytes; upon egg activation, YA acquires the ability to enter nuclei and becomes incorporated into the nuclear lamina in unfertilized eggs and embryos. This localization switch correlates with changes in the phosphorylation state of YA. YA in ovaries is hyperphosphorylated relative to YA in unfertilized eggs and embryos. Through site-directed mutagenesis, we identified 443T, a potential phosphorylation site for both cyclin-dependent protein kinase and mitogen-activated-protein kinase, as one of the sites likely involved in this developmental control. Our results suggest that phosphorylation plays a role in modulating the localization of YA during development. A model for developmental regulation of the nuclear entry of YA is proposed and implications for understanding Drosophila egg activation are discussed.
|Number of pages||11|
|Publication status||Published - 1999 Jun 1|
Bibliographical noteFunding Information:
We thank P. Fisher for polyclonal anti-lamin and H. Saumweber for mouse monoclonal anti-lamin antibodies, and M. L. Goldberg and W. J. Brown for useful discussions and advice. K. J. Kemphues, E. E. Alani, Y. Heifetz, E. Andrulis, O. Lung, U. Tram, and C. L. Berman provided helpful comments on the manuscript. This work was supported by National Institutes of Health Grant GM44659 to M.F.W. During part of this work, S.G.T. was supported on NIH Training Grant GM07273.
All Science Journal Classification (ASJC) codes
- Molecular Biology
- Developmental Biology
- Cell Biology