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Vol. 20, Issue 19, 4246-4255, October 1, 2009

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Dissection of CENP-C–directed Centromere and Kinetochore Assembly

Department of Biochemistry, Stanford University School of Medicine, Stanford, CA 94305

Submitted May 8, 2009; Revised July 13, 2009; Accepted July 22, 2009
Monitoring Editor: Kerry S. Bloom

Eukaryotic cells ensure accurate chromosome segregation in mitosis by assembling a microtubule-binding site on each chromosome called the kinetochore that attaches to the mitotic spindle. The kinetochore is assembled specifically during mitosis on a specialized region of each chromosome called the centromere, which is constitutively bound by >15 centromere-specific proteins. These proteins, including centromere proteins A and C (CENP-A and -C), are essential for kinetochore assembly and proper chromosome segregation. How the centromere is assembled and how the centromere promotes mitotic kinetochore formation are poorly understood. We have used Xenopus egg extracts as an in vitro system to study the role of CENP-C in centromere and kinetochore assembly. We show that, unlike the histone variant CENP-A, CENP-C is not maintained at centromeres through spermatogenesis but is assembled at the sperm centromere from the egg cytoplasm. Immunodepletion of CENP-C from metaphase egg extract prevents kinetochore formation on sperm chromatin, and depleted extracts can be complemented with in vitro–translated CENP-C. Using this complementation assay, we have identified CENP-C mutants that localized to centromeres but failed to support kinetochore assembly. We find that the amino terminus of CENP-C promotes kinetochore assembly by ensuring proper targeting of the Mis12/MIND complex and CENP-K.

Address correspondence to: Aaron F. Straight (astraigh{at}stanford.edu).

Abbreviations used: C-, carboxy; CENP, centromere protein; CSF, cytostatic factor; IVT, in vitro transcription/translation; N-, amino.