Posttranslational control of Cdc25 degradation terminates Drosophila's early cell-cycle program.

TitlePosttranslational control of Cdc25 degradation terminates Drosophila's early cell-cycle program.
Publication TypeJournal Article
Year of Publication2013
AuthorsDi Talia, S, She, R, Blythe, SA, Lu, X, Zhang, QFan, Wieschaus, EF
JournalCurr Biol
Date Published2013 Jan 21
KeywordsAnimals, cdc25 Phosphatases, Cell Cycle, Cell Cycle Proteins, Drosophila, Drosophila Proteins, Embryonic Development, Protein Processing, Post-Translational, Protein Tyrosine Phosphatases

<p>In most metazoans, early embryonic development is characterized by rapid mitotic divisions that are controlled by maternal mRNAs and proteins that accumulate during oogenesis. These rapid divisions pause at the midblastula transition (MBT), coinciding with a dramatic increase in gene transcription and the degradation of a subset of maternal mRNAs. In Drosophila, the cell-cycle pause is controlled by inhibitory phosphorylation of Cdk1, which in turn is driven by downregulation of the activating Cdc25 phosphatases. Here, we show that the two Drosophila Cdc25 homologs, String and Twine, differ in their dynamics and that, contrary to current models, their downregulations are not controlled by mRNA degradation but through different posttranslational mechanisms. The degradation rate of String protein gradually increases during the late syncytial cycles in a manner dependent on the nuclear-to-cytoplasmic ratio and on the DNA replication checkpoints. Twine, on the other hand, is targeted for degradation at the onset of the MBT through a switch-like mechanism controlled, like String, by the nuclear-to-cytoplasmic ratio, but not requiring the DNA replication checkpoints. We demonstrate that posttranslational control of Twine degradation ensures that the proper number of mitoses precede the MBT.</p>

Alternate JournalCurr Biol
PubMed ID23290553
PubMed Central IDPMC3622868
Grant List / HHMI / Howard Hughes Medical Institute / United States
5R37HD15587 / HD / NICHD NIH HHS / United States
F32 HD072653 / HD / NICHD NIH HHS / United States
1F32HD072653 / HD / NICHD NIH HHS / United States
R37 HD015587 / HD / NICHD NIH HHS / United States