Department of Chemistry and Biochemistry, University of Colorado, Boulder, Colorado 80309, USA.
Annu Rev Biochem. 2012;81:561-85. doi: 10.1146/annurev-biochem-061611-090435. Epub 2012 Apr 5.
MPS1 protein kinases are found widely, but not ubiquitously, in eukaryotes. This family of potentially dual-specific protein kinases is among several that regulate a number of steps of mitosis. The most widely conserved MPS1 kinase functions involve activities at the kinetochore in both the chromosome attachment and the spindle checkpoint. MPS1 kinases also function at centrosomes. Beyond mitosis, MPS1 kinases have been implicated in development, cytokinesis, and several different signaling pathways. Family members are identified by virtue of a conserved C-terminal kinase domain, though the N-terminal domain is quite divergent. The kinase domain of the human enzyme has been crystallized, revealing an unusual ATP-binding pocket. The activity, level, and subcellular localization of Mps1 family members are tightly regulated during cell-cycle progression. The mitotic functions of Mps1 kinases and their overexpression in some tumors have prompted the identification of Mps1 inhibitors and their active development as anticancer drugs.
MPS1 蛋白激酶在真核生物中广泛存在,但并非普遍存在。这个潜在的双特异性蛋白激酶家族是调节有丝分裂多个步骤的几个家族之一。最广泛保守的 MPS1 激酶功能涉及到染色体附着和纺锤体检查点的动粒中的活性。MPS1 激酶也在中心体中发挥作用。除了有丝分裂,MPS1 激酶还与发育、胞质分裂和几种不同的信号通路有关。家族成员通过保守的 C 末端激酶结构域来识别,尽管 N 末端结构域非常不同。人类酶的激酶结构域已经被结晶,揭示了一个不寻常的 ATP 结合口袋。Mps1 家族成员的活性、水平和亚细胞定位在细胞周期进展过程中受到严格调节。Mps1 激酶的有丝分裂功能及其在某些肿瘤中的过度表达促使人们鉴定出 Mps1 抑制剂,并积极将其开发为抗癌药物。