CAL1 is the Drosophila CENP-A assembly factor

Author:

Chen Chin-Chi1,Dechassa Mekonnen Lemma2,Bettini Emily1,Ledoux Mary B.1,Belisario Christian1,Heun Patrick3,Luger Karolin22,Mellone Barbara G.1

Affiliation:

1. Department of Molecular and Cell Biology, University of Connecticut, Storrs, CT 06269

2. Department of Biochemistry and Molecular Biology, Howard Hughes Medical Institute, Colorado State University, Fort Collins, CO 80523

3. Max-Planck-Institute of Immunobiology and Epigenetics, 79108 Freiburg, Germany

Abstract

Centromeres are specified epigenetically by the incorporation of the histone H3 variant CENP-A. In humans, amphibians, and fungi, CENP-A is deposited at centromeres by the HJURP/Scm3 family of assembly factors, but homologues of these chaperones are absent from a number of major eukaryotic lineages such as insects, fish, nematodes, and plants. In Drosophila, centromeric deposition of CENP-A requires the fly-specific protein CAL1. Here, we show that targeting CAL1 to noncentromeric DNA in Drosophila cells is sufficient to heritably recruit CENP-A, kinetochore proteins, and microtubule attachments. CAL1 selectively interacts with CENP-A and is sufficient to assemble CENP-A nucleosomes that display properties consistent with left-handed octamers. The CENP-A assembly activity of CAL1 resides within an N-terminal domain, whereas the C terminus mediates centromere recognition through an interaction with CENP-C. Collectively, this work identifies the “missing” CENP-A chaperone in flies, revealing fundamental conservation between insect and vertebrate centromere-specification mechanisms.

Publisher

Rockefeller University Press

Subject

Cell Biology

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