The F-box Protein Rcy1 Is Involved in the Degradation of Histone H3 Variant Cse4 and Genome Maintenance*
- Haili Cheng,
- Xin Bao and
- Hai Rao1
- From the Department of Molecular Medicine, University of Texas Health Science Center at San Antonio, San Antonio, Texas 78229
- ↵1 To whom correspondence should be addressed: 7703 Floyd Curl Dr., San Antonio, TX 78229. Tel.: 210-562-4149; Fax: 210-562-4161; E-mail: raoh{at}uthscsa.edu.
Abstract
Cse4, a histone H3-like centromeric protein, plays critical functions in chromosome segregation. Cse4 level is tightly regulated, but the underlying mechanism remains poorly understood. We employed a toxicity-based screen to look for the degradation components involved in Cse4 regulation. Here, we show that the F-box containing protein Rcy1 is required for efficient Cse4 turnover as Cse4 degradation is compromised in yeast cells lacking RCY1. Excessive Cse4 accumulation in rcy1Δ cells leads to growth retardation. Furthermore, the deletion of RCY1 is tied to enhanced chromosome instability and temperature-sensitive cell growth. Our results reveal the involvement of Rcy1 in chromosome regulation and another regulatory pathway controlling the Cse4 level and activity.
Footnotes
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↵* This work was supported by Welch Foundation Grant AQ 1747, the William & Ella Owens Medical Research Foundation, the Helen F. Kerr Foundation, Department of Defense Grant W911NF-11-10466, and National Institutes of Health Grant GM 078085 (to H. R.). The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health. The authors declare that there is no conflict of interest for this study.
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This article contains supplemental Table S1.
- Received November 2, 2015.
- Revision received March 8, 2016.
- © 2016 by The American Society for Biochemistry and Molecular Biology, Inc.











