Abstract

The centromere-specific histone CENP-A is the key epigenetic determinant of centromere identity. Whereas most histones are removed from mature sperm, CENP-A is retained to mark paternal centromeres. In Drosophila males we show that the centromere assembly factors CAL1 and CENP-C are required for meiotic chromosome segregation, CENP-A assembly and maintenance on sperm, as well as fertility. In meiosis, CENP-A accumulates with CAL1 in nucleoli. Furthermore, we show that CENP-C normally limits the release of CAL1 and CENP-A from nucleoli for proper centromere assembly in meiotic prophase I. Finally, we show that RNA polymerase I transcription is required for efficient CENP-A assembly in meiosis, as well as centromere tethering to nucleoli.

Highlights

  • Centromeres are chromosomal loci where microtubules attach to ensure proper chromosome segregation at cell division

  • Quantitation of tubulin staining in Cenp-CZ3-4375/TM3 and cal12k32/TM3 spermatocytes revealed that both mutants had defective spindle morphologies in meiosis I and II compared with wild type (Fig. S1B), which was likely to be due to roles of CENP-C and CAL1 in centromere/kinetochore assembly

  • We have analysed the effects of mutations in the key centromere assembly factors, Cenp-C and cal1, on Drosophila male meiosis

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Summary

Introduction

Centromeres are chromosomal loci where microtubules attach to ensure proper chromosome segregation at cell division. CENP-A is assembled and maintained to ensure centromere propagation (Valente et al, 2012). Studies of the cell cycle timing of CENP-A assembly and the discovery of CENP-A-specific assembly factors have provided great insights into the mechanisms of CENP-A assembly in mitosis (Dunleavy et al, 2009; Foltz et al, 2009; Müller and Almouzni, 2014). Mechanisms of meiotic CENP-A assembly are emerging and differ from those of mitosis. In Drosophila males, CENP-A [ known as Centromere identifier (CID) – FlyBase] is assembled at meiotic prophase I and again during spermatid differentiation

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