Instituto de Biología Molecular y Celular del Cáncer, Consejo Superior de Investigaciones Científicas (CSIC) - Universidad de Salamanca, Salamanca, Spain.
Instituto de Investigación Biomédica de Salamanca (IBSAL), Hospital Universitario de Salamanca, Salamanca, Spain.
Nucleus. 2024 Dec;15(1):2353249. doi: 10.1080/19491034.2024.2353249. Epub 2024 May 16.
In the nucleus, the VRK1 Ser-Thr kinase is distributed in nucleoplasm and chromatin, where it has different roles. VRK1 expression increases in response to mitogenic signals. VRK1 regulates cyclin D1 expression at G0 exit and facilitates chromosome condensation at the end of G2 and G2/M progression to mitosis. These effects are mediated by the phosphorylation of histone H3 at Thr3 by VRK1, and later in mitosis by haspin. VRK1 regulates the apigenetic patterns of histones in processes requiring chromating remodeling, such as transcription, replication and DNA repair. VRK1 is overexpressed in tumors, facilitating tumor progression and resistance to genotoxic treatments. VRK1 also regulates the organization of Cajal bodies assembled on coilin, which are necessary for the assembly of different types of RNP complexes. VRK1 pathogenic variants cuase defects in Cajal bodies, functionally altering neurons with long axons and leading to neurological diseases, such as amyotrophic laterla sclerosis, spinal muscular atrophy, distal hereditay motor neuropathies and Charcot-Marie-Tooth.
在细胞核中,VRK1 Ser-Thr 激酶分布在核质和染色质中,在那里它有不同的作用。VRK1 的表达会随着有丝分裂信号的增加而增加。VRK1 在 G0 出口处调节细胞周期蛋白 D1 的表达,并促进 G2 末期和 G2/M 向有丝分裂的染色体浓缩。这些作用是由 VRK1 对组蛋白 H3 的 Thr3 进行磷酸化介导的,在有丝分裂后期则由 haspin 介导。VRK1 调节染色质重塑过程中组蛋白的表观遗传模式,如转录、复制和 DNA 修复。VRK1 在肿瘤中过度表达,促进肿瘤的进展和对遗传毒性治疗的耐药性。VRK1 还调节 coilin 上组装的 Cajal 体的组织,这对于不同类型的 RNP 复合物的组装是必要的。VRK1 的致病性变异导致 Cajal 体缺陷,功能性改变长轴突神经元,导致神经疾病,如肌萎缩侧索硬化症、脊髓性肌萎缩症、远端遗传性运动神经病和 Charcot-Marie-Tooth 病。