Niwa H, Abe K, Kunisada T, Yamamura K
Department of Developmental Genetics, Kumamoto University School of Medicine, Japan.
Gene. 1996 Mar 9;169(2):197-201. doi: 10.1016/0378-1119(95)00809-8.
We have cloned a novel putative serine/threonine kinase-encoding gene, designed STK-1, from murine embryonic stem (ES) cell and testis cDNA libraries. The kinase most closely related to STK-1 is Xenopus laevis XLP46 protein kinase which shows 71% amino-acid identity to STK-1 between their kinase domains. Nevertheless, STK-1 is conserved throughout phylogeny with hybridizing sequences being detected in DNA from mammals, amphibians, insects and yeast. STK-1 mRNA is detected in testis, intestine and spleen, tissues that contain a large number of proliferating cells, but not in other tissues. All cell lines tested expressed STK-1 mRNA with levels being dependent upon proliferation rates. In NIH 3T3 cells, STK-1 is expressed in a cell-cycle-dependent fashion. These findings suggest a role for STK-1 in cell growth.
我们从鼠胚胎干细胞和睾丸cDNA文库中克隆了一个新的假定的丝氨酸/苏氨酸激酶编码基因,命名为STK-1。与STK-1关系最密切的激酶是非洲爪蟾XLP46蛋白激酶,其激酶结构域之间与STK-1的氨基酸同一性为71%。然而,STK-1在整个系统发育过程中是保守的,在哺乳动物、两栖动物、昆虫和酵母的DNA中都检测到了杂交序列。在睾丸、肠道和脾脏中检测到STK-1 mRNA,这些组织含有大量增殖细胞,而在其他组织中未检测到。所有测试的细胞系都表达STK-1 mRNA,其水平取决于增殖速率。在NIH 3T3细胞中,STK-1以细胞周期依赖性方式表达。这些发现表明STK-1在细胞生长中起作用。