1. Academic Validation
  2. RNAi knockdown of human kinetochore protein CENP-H

RNAi knockdown of human kinetochore protein CENP-H

  • Biochem Biophys Res Commun. 2006 Sep 15;348(1):36-46. doi: 10.1016/j.bbrc.2006.06.187.
Sandra Orthaus 1 Sabine Ohndorf Stephan Diekmann
Affiliations

Affiliation

  • 1 Department of Molecular Biology, FLI e.V., Beutenbergstrasse 11, D-07745 Jena, Germany.
Abstract

The inner kinetochore protein complex binds to centromeres during the whole cell cycle. It serves as the basis for the binding of further kinetochore proteins during mitosis. CENP-H is one of the inner kinetochore proteins which is conserved amongst many eukaryotes. By specific RNAi knockdown, we reduced the CENP-H protein level in human HEp-2 cells down to less than 5% of its normal value. In these CENP-H knocked-down cells, we observed severe mitotic phenotypes like misaligned chromosomes and multipolar spindles, however, no mitotic arrest. Strong reduction of CENP-H resulted in a slightly reduced CENP-C level at the kinetochores and normal localisation of hBubR1, indicating a functional mitotic checkpoint at the hBubR1 protein level. In CENP-H knocked-down human cells, the misaligned chromosomes contained only reduced levels of CENP-E. Our data clearly indicate that CENP-H has an important impact on the architecture and function of the human kinetochore complex.

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