A novel DYRK1B inhibitor AZ191 demonstrates that DYRK1B acts independently of GSK3 beta to phosphorylate cyclin D1 at Thr(286), not Thr(288)

作者：Ashford Anne L^*; Oxley David; Kettle Jason; Hudson Kevin; Guichard Sylvie; Cook Simon J; Lochhead Pamela A

来源：Biochemical Journal, 2014, 457(1): 43-56.

DOI：10.1042/BJ20130461

• AZ191
• cell cycle
• cyclin D1
• dual-specificity tyrosine phosphorylation-regulated kinase 1B (DYRK1B)
• glycogen synthase kinase 3 beta (GSK3 beta)

DYRK1B (dual-specificity tyrosine phosphorylation-regulated kinase 1B) is amplified in certain cancers and may be an oncogene; however, our knowledge of DYRK1B has been limited by the lack of selective inhibitors. In the present study we describe AZ191, a potent small molecule inhibitor that selectively inhibits DYRK1B in vitro and in cells. CCND1 (cyclin D1), a key regulator of the mammalian G(1)-S-phase transition, is phosphorylated on Thr(286) by GSK3 beta (glycogen synthase kinase 3 beta) to promote its degradation. DYRK1B has also been proposed to promote CCND1 turnover, but was reported to phosphorylate Thr(288) rather than Thr(286). Using in vitro kinase assays, phospho-specific immunoblot analysis and MS in conjunction with AZ191 we now show that DYRK1B phosphorylates CCND1 at Thr(286), not Thr(288), in vitro and in cells. In HEK (human embryonic kidney)-293 and PANC-1 cells (which exhibit DYRK1B amplification) DYRK1B drives Thr(286) phosphorylation and proteasome-dependent turnover of CCND1 and this is abolished by AZ191 or DYRK1B RNAi, but not by GSK3 beta inhibitors or GSK3 beta RNAi. DYRK1B expression causes a G(1)-phase cell-cycle arrest, but overexpression of CCND1 (wild-type or T286A) fails to overcome this; indeed, DYRK1B also promotes the expression of p21(CIPI) (21 kDa CDK-interacting protein 1) and p27(KIPI) (CDK-inhibitory protein 1). The results of the present study demonstrate for the first time that DYRK1B is a novel Thr(286)-CCND1 kinase that acts independently of GSK3 beta to promote CCND1 degradation. Furthermore, we anticipate that AZ191 may prove useful in defining further substrates and biological functions of DYRK1B.

• 出版日期2014-1-1