4.7 Article

The Structure of the Plk4 Cryptic Polo Box Reveals Two Tandem Polo Boxes Required for Centriole Duplication

Journal

STRUCTURE
Volume 20, Issue 11, Pages 1905-1917

Publisher

CELL PRESS
DOI: 10.1016/j.str.2012.08.025

Keywords

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Funding

  1. National Cancer Institute [P30 CA23074]
  2. American Cancer Society [IRG 74-001-31]
  3. GI SPORE [NCI/NIH P50 CA95060]
  4. Arizona Biomedical Research Commission (ABRC) [1210]
  5. March of Dimes Basil O'Connor Award [5-FY10-44]
  6. National Institutes of Health [5R03HD064881, 1R01GM094415]
  7. National Science Foundation Graduate Research Fellowship [DGE-0646083]

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Centrioles are key microtubule polarity determinants. Centriole duplication is tightly controlled to prevent cells from developing multipolar spindles, a situation that promotes chromosomal instability. A conserved component in the duplication pathway is Plk4, a polo kinase family member that localizes to centrioles in M/G1. To limit centriole duplication, Plk4 levels are controlled through trans-autophosphorylation that primes ubiquitination. In contrast to Plks 1-3, Plk4 possesses a unique central region called the cryptic polo box. Here, we present the crystal structure of this region at 2.3 angstrom resolution. Surprisingly, the structure reveals two tandem homodimerized polo boxes, PB1-PB2, that form a unique winged architecture. The full PB1-PB2 cassette is required for binding the centriolar protein Asterless as well as robust centriole targeting. Thus, with its C-terminal polo box (PB3), Plk4 has a triple polo box architecture that faciltates oligomerization, targeting, and promotes trans-autophosphorylation, limiting centriole duplication to once per cell cycle.

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