4.8 Article

Drosophila CENH3 Is Sufficient for Centromere Formation

Journal

SCIENCE
Volume 334, Issue 6056, Pages 686-690

Publisher

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.1206880

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Funding

  1. Deutsche Forschungsgemeinschaft [Sonderforschungsbereich (SFB) 646, SFB/TR05, Schwerpunktprogramm 1230]
  2. Max Planck Society
  3. Human Frontier Science Program
  4. Excellence Initiative of the German Federal Government [EXC 294]
  5. Excellence Initiative of the German State Government [EXC 294]
  6. Max Planck Institute of Immunobiology and Epigenetics

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CENH3 is a centromere-specific histone H3 variant essential for kinetochore assembly. Despite its central role in centromere function, there has been no conclusive evidence supporting CENH3 as sufficient to determine centromere identity. To address this question, we artificially targeted Drosophila CENH3 (CENP-A/CID) as a CID-GFP-LacI fusion protein to stably integrated lac operator (lacO) arrays. This ectopic CID focus assembles a functional kinetochore and directs incorporation of CID molecules without the LacI-anchor, providing evidence for the self-propagation of the epigenetic mark. CID-GFP-LacI-bound extrachromosomal lacO plasmids can assemble kinetochore proteins and bind microtubules, resulting in their stable transmission for several cell generations even after eliminating CID-GFP-LacI. We conclude that CID is both necessary and sufficient to serve as an epigenetic centromere mark and nucleate heritable centromere function.

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