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HSF1 as a Mitotic Regulator: Phosphorylation of HSF1 by Plk1 Is Essential for Mitotic Progression

Divisions of ¹ Radiation Effects and ² Radiation Cancer Research, Korea Institute of Radiological and Medical Sciences, Seoul, Korea; ³ College of Natural Sciences, Kangwon National University, and ⁴ Korea Basic Science Institute, Chunchon Center, Chunchon, Korea

Requests for reprints: Yun-Sil Lee, Division of Radiation Effects, Korea Institute of Radiological and Medical Sciences, 215-4 Gongneung-Dong, Nowon-Ku, Seoul 139-706, Korea. Phone: 82-2970-1325; Fax: 82-2970-2402; E-mail: yslee{at}kcch.re.kr.

Key Words: HSF1 • Mitosis progression • Plk1 • SCF^β-TrCP

Previously, heat shock factor 1 (HSF1) had been reported to induce genomic instability and aneuploidy by interaction with Cdc20. Here, we have further examined the functions of HSF1 in the regulation of mitosis. A null mutant or knockdown of HSF1 caused defective mitotic progression. By monitoring chromosomes in living cells, we determined that HSF1 was localized to the centrosome in mitosis and especially to the spindle poles in metaphase. HSF1 was phosphorylated by Plk1 at Ser²¹⁶ of the DSGXXS motif during the timing of mitosis and a phospho-defective mutant form of HSF1 inhibited mitotic progression. Phosphorylated HSF1 during spindle pole localization underwent ubiquitin degradation through the SCF^β-TrCP pathway. However, binding of HSF1 with Cdc20 stabilized the phosphorylation of HSF1. Moreover, SCF^β-TrCP–mediated degradation only occurred when phosphorylated HSF1 was released from Cdc20. HSF1 phosphorylation at Ser²¹⁶ occurred in the early mitotic period with simultaneous binding of Cdc20. The interaction of HSF1 with SCF^β-TrCP was followed and then the interaction of APC/Cdc20 was subsequently observed. From these findings, it was shown that Plk1 phosphorylates HSF1 in early mitosis and that the binding of phosphorylated HSF1 with Cdc20 and ubiquitin degradation by SCF^β-TrCP regulates mitotic progression. [Cancer Res 2008;68(18):7550–60]