Department of Biology, Lone Star College, Woodlands, TX 77375, USA.
Department of Biological Sciences, Sam Houston State University, Huntsville, TX 77341, USA.
Int J Mol Sci. 2017 Dec 28;19(1):72. doi: 10.3390/ijms19010072.
Aurora kinases (AKs) are serine/threonine kinases that are essential for cell division. Humans have three AK genes: , , and . AKA is required for centrosome assembly, centrosome separation, and bipolar spindle assembly, and its mutation leads to abnormal spindle morphology. AKB is required for the spindle checkpoint and proper cytokinesis, and mutations cause chromosome misalignment and cytokinesis failure. AKC is expressed in germ cells, and has a role in meiosis analogous to that of AKB in mitosis. Mutation of any of the three isoforms can lead to cancer. AK proteins possess divergent N- and C-termini and a conserved central catalytic domain. We examined the evolution of the AK gene family using an identity matrix and by building a phylogenetic tree. The data suggest that is the vertebrate ancestral gene, and that and resulted from gene duplication in placental mammals. In a nonsynonymous/synonymous rate substitution analysis, we found that experienced the strongest, and the weakest, purifying selection. Both the N- and C-termini and regions within the kinase domain experienced differential selection among the AK isoforms. These differentially selected sequences may be important for species specificity and isoform specificity, and are therefore potential therapeutic targets.
极光激酶(AKs)是丝氨酸/苏氨酸激酶,对细胞分裂至关重要。人类有三个 AK 基因:、和。AKA 对于中心体组装、中心体分离和双极纺锤体组装是必需的,其突变会导致纺锤体形态异常。AKB 对于纺锤体检查点和正常胞质分裂是必需的,突变会导致染色体错位和胞质分裂失败。AKC 在生殖细胞中表达,在减数分裂中具有类似于 AKB 在有丝分裂中的作用。三种异构体中的任何一种突变都可能导致癌症。AK 蛋白具有不同的 N 端和 C 端以及保守的中央催化结构域。我们使用同一性矩阵和构建系统发育树来研究 AK 基因家族的进化。数据表明,是脊椎动物的祖先基因,和是胎盘哺乳动物基因复制的结果。在非同义/同义替代率替代分析中,我们发现经历了最强的、最弱的纯化选择。AK 异构体之间的 N 端和 C 端以及激酶结构域内的区域都经历了差异选择。这些差异选择的序列可能对物种特异性和同工型特异性很重要,因此是潜在的治疗靶点。