Kuwano Yuki, Nishida Kensei, Akaike Yoko, Kurokawa Ken, Nishikawa Tatsuya, Masuda Kiyoshi, Rokutan Kazuhito
Department of Pathophysiology, Institute of Biomedical Sciences, Tokushima University Graduate School, 3-18-15 Kuramoto-cho, Tokushima 770-8503, Japan.
Int J Mol Sci. 2016 Sep 27;17(10):1638. doi: 10.3390/ijms17101638.
Homeodomain-interacting protein kinase 2 (HIPK2) is a serine/threonine kinase that phosphorylates and activates the apoptotic program through interaction with diverse downstream targets including tumor suppressor p53. HIPK2 is activated by genotoxic stimuli and modulates cell fate following DNA damage. The DNA damage response (DDR) is triggered by DNA lesions or chromatin alterations. The DDR regulates DNA repair, cell cycle checkpoint activation, and apoptosis to restore genome integrity and cellular homeostasis. Maintenance of the DDR is essential to prevent development of diseases caused by genomic instability, including cancer, defects of development, and neurodegenerative disorders. Recent studies reveal a novel HIPK2-mediated pathway for DDR through interaction with chromatin remodeling factor homeodomain protein 1γ. In this review, we will highlight the molecular mechanisms of HIPK2 and show its functions as a crucial DDR regulator.
同源结构域相互作用蛋白激酶2(HIPK2)是一种丝氨酸/苏氨酸激酶,它通过与包括肿瘤抑制因子p53在内的多种下游靶点相互作用来磷酸化并激活凋亡程序。HIPK2由基因毒性刺激激活,并在DNA损伤后调节细胞命运。DNA损伤反应(DDR)由DNA损伤或染色质改变触发。DDR调节DNA修复、细胞周期检查点激活和凋亡,以恢复基因组完整性和细胞稳态。维持DDR对于预防由基因组不稳定引起的疾病(包括癌症、发育缺陷和神经退行性疾病)的发生至关重要。最近的研究揭示了一种通过与染色质重塑因子同源结构域蛋白1γ相互作用的新型HIPK2介导的DDR途径。在本综述中,我们将重点介绍HIPK2的分子机制,并展示其作为关键DDR调节因子的功能。