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Targeting Polo-like kinase in space and time during C. elegans meiosis.

James N BrandtYumi Kim
Published in: Cell cycle (Georgetown, Tex.) (2021)
A central player in meiotic chromosome dynamics is the conserved Polo-like kinase (PLK) family. PLKs are dynamically localized to distinct structures during meiotic prophase and phosphorylate a diverse group of substrates to control homolog pairing, synapsis, and meiotic recombination. In a recent study, we uncovered the mechanisms that control the targeting of a meiosis-specific PLK-2 in C. elegans. In early meiotic prophase, PLK-2 localizes to special chromosome regions known as pairing centers and drives homolog pairing and synapsis. PLK-2 then relocates to the synaptonemal complex (SC) after crossover designation and mediates chromosome remodeling required for homolog separation. What controls this intricate targeting of PLK-2 in space and time? We discuss recent findings and remaining questions for the future.
Keyphrases
  • cancer therapy
  • copy number
  • tyrosine kinase
  • dna damage
  • transcription factor
  • randomized controlled trial
  • gene expression
  • drug delivery
  • oxidative stress
  • open label
  • dna methylation
  • placebo controlled