Klerkx E P F, Lazo P A, Askjaer P
Andalusian Centre for Developmental Biology (CABD), Spanish National Research Council (CSIC)-Pablo de Olavide University (UPO), Seville, Spain.
Histol Histopathol. 2009 Jun;24(6):749-59. doi: 10.14670/HH-24.749.
The vaccinia-related kinases (VRKs) branched off early from the family of casein kinase (CK) I and compose a relatively uncharacterized family of the kinome. The VRKs were discovered due to their close sequence relation to the vaccinia virus B1R serine/threonine kinase. They were first described in phosphorylation of transcription factors that led to the discovery of an autoregulatory mechanism between VRK and the tumor suppressor transcription factor p53. The relevance of VRKs has broadened recently by introduction of its members as essential regulators in cell signaling, nuclear envelope dynamics, chromatin modifications, apoptosis and cellular stress response. Several phosphorylation substrates have been described, as well as the first positive and negative regulators of VRK. We provide an overview of the VRKs across species and discuss the wide diversity of cellular and organismal requirements for this kinase family.
痘苗相关激酶(VRK)较早从酪蛋白激酶(CK)I家族中分化出来,构成了激酶组中一个相对未被充分研究的家族。VRK因其与痘苗病毒B1R丝氨酸/苏氨酸激酶的密切序列关系而被发现。它们最初是在转录因子的磷酸化过程中被描述的,这导致了VRK与肿瘤抑制转录因子p53之间一种自动调节机制的发现。最近,通过将其成员引入细胞信号传导、核膜动态、染色质修饰、细胞凋亡和细胞应激反应中的关键调节因子,VRK的相关性得到了扩展。已经描述了几种磷酸化底物以及VRK的首个正向和负向调节因子。我们概述了跨物种的VRK,并讨论了该激酶家族在细胞和机体需求方面的广泛多样性。