Chen A, Yanai A, Arama E, Kilfin G, Motro B
Faculty of Life Sciences, Bar-Ilan University, Ramat-Gan 52900, Israel.
Gene. 1999 Jun 24;234(1):127-37. doi: 10.1016/s0378-1119(99)00165-1.
The Aspergillus NIMA kinase plays a key role in controlling entrance into mitosis, and recent evidence suggests that mammalian NIMA-related kinases perform similar functions. We report here the cloning of the mouse nek3 and nek4 genes. Mouse nek3 is probably the ortholog of the partially sequenced, human nek3, whereas murine nek4 cDNA is probably the ortholog of human STK2. Nek4 is highly conserved between mouse and human, whereas Nek3 is somewhat less conserved (96.5 and 88% identity in the kinase domains, respectively). Northern analysis shows preferential expression of nek3 in mitotically active tissue, whereas nek4 is highly abundant in the testis. Within the developing testicular germ cells, in-situ analysis demonstrated that nek1, 2 and 4 exhibit differential patterns of expression, suggesting overlapping, but non-identical functions. Linkage analysis, using the mouse recombinant inbred strain panel (BXD), was used to localize nek1, 2 and 3. nek1 was mapped between Cpe and D8Mit8 on chromosome 8 at around 32cM, nek2 was mapped to the distal region of chromosome 1, and nek3 was mapped to the most centromeric region of chromosome 8.
构巢曲霉NIMA激酶在控制进入有丝分裂过程中起关键作用,最近的证据表明哺乳动物NIMA相关激酶执行类似功能。我们在此报告小鼠nek3和nek4基因的克隆。小鼠nek3可能是部分测序的人类nek3的直系同源物,而小鼠nek4 cDNA可能是人类STK2的直系同源物。Nek4在小鼠和人类之间高度保守,而Nek3的保守性稍低(激酶结构域中的同一性分别为96.5%和88%)。Northern分析显示nek3在有丝分裂活跃组织中优先表达,而nek4在睾丸中高度丰富。在发育中的睾丸生殖细胞内,原位分析表明nek1、2和4表现出不同的表达模式,提示功能重叠但不完全相同。使用小鼠重组近交系面板(BXD)进行连锁分析,以定位nek1、2和3。nek1定位于8号染色体上Cpe和D8Mit8之间约32cM处,nek2定位于1号染色体的远端区域,nek3定位于8号染色体的最着丝粒区域。