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First published online 16 January 2008
doi: 10.1242/dev.013425

This Article Figures Only Full Text Full Text (PDF) All Versions of this Article: dev.013425v1 135/4/687    most recent Alert me when this article is cited Alert me if a correction is posted Services Email this article to a friend Related articles in Development Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via HighWire Google Scholar Articles by Nishi, Y. Articles by Lin, R. PubMed PubMed Citation Articles by Nishi, Y. Articles by Lin, R.

Polo kinases regulate C. elegans embryonic polarity via binding to DYRK2-primed MEX-5 and MEX-6

Yuichi Nishi^*,, Eric Rogers^*, Scott M. Robertson and Rueyling Lin

Department of Molecular Biology, University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, TX 75390, USA.

Author for correspondence (e-mail: Rueyling.Lin{at}UTSouthwestern.edu)

Accepted 19 November 2007

Polo kinases are known key regulators of cell divisions. Here we report a novel, non-cell division function for polo kinases in embryonic polarity of newly fertilized Caenorhabditis elegans embryos. We show that polo kinases, via their polo box domains, bind to and regulate the activity of two key polarity proteins, MEX-5 and MEX-6. These polo kinases are asymmetrically localized along the anteroposterior axis of newly fertilized C. elegans embryos in a pattern identical to that of MEX-5 and MEX-6. This asymmetric localization of polo kinases depends on MEX-5 and MEX-6, as well as genes regulating MEX-5 and MEX-6 asymmetry. We identify an amino acid of MEX-5, T₁₈₆, essential for polo binding and show that T₁₈₆ is important for MEX-5 function in vivo. We also show that MBK-2, a developmentally regulated DYRK2 kinase activated at meiosis II, primes T₁₈₆ for subsequent polo kinase-dependent phosphorylation. Prior phosphorylation of MEX-5 at T₁₈₆ greatly enhances phosphorylation of MEX-5 by polo kinases in vitro. Our results provide a mechanism by which MEX-5 and MEX-6 function is temporally regulated during the crucial oocyte-to-embryo transition.

Key words: Caenorhabditis elegans, MEX-5, Embryo, Polarity, Polo kinase

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