Howard O M, Dean M, Young H, Ramsburg M, Turpin J A, Michiel D F, Kelvin D J, Lee L, Farrar W L
Biological Carcinogenesis and Development Program, Program Resources, Inc/DynCorp, Frederick, Maryland 21702.
Oncogene. 1992 May;7(5):895-900.
In an effort to identify unique tyrosine kinases found in human leukemia cell lines, we utilized polymerase chain reaction (PCR) technology and degenerate oligonucleotide primers to produce a cDNA library of kinase catalytic domains found in the human monocytic cell line AML-193. This search yielded a member of the class 3 tyrosine kinases closely related to the murine kinase FD-22. Previous work has identified this kinase as JAK1. This class of tyrosine kinases is characterized by being ubiquitously expressed, lacking both a ligand-binding domain and a SH2 domain, while containing a second domain similar to a degenerate kinase domain. Our studies focused on the further characterization of this class 3 tyrosine kinase using Northern blot analysis to demonstrate an increase in steady-state mRNA by interferon-gamma in human monocytes. A human-hamster somatic cell hybrid panel and linkage mapping was used to assign JAK1 (aml-116) to human chromosome 1.
为了鉴定人类白血病细胞系中发现的独特酪氨酸激酶,我们利用聚合酶链反应(PCR)技术和简并寡核苷酸引物,构建了人类单核细胞系AML - 193中激酶催化结构域的cDNA文库。这项研究发现了一个与鼠源激酶FD - 22密切相关的3类酪氨酸激酶成员。先前的研究已将该激酶鉴定为JAK1。这类酪氨酸激酶的特点是广泛表达,既没有配体结合结构域也没有SH2结构域,同时含有一个类似于简并激酶结构域的第二结构域。我们的研究集中在使用Northern印迹分析进一步表征这种3类酪氨酸激酶,以证明干扰素 - γ可使人类单核细胞中的稳态mRNA增加。利用人类 - 仓鼠体细胞杂交板和连锁图谱分析,将JAK1(aml - 116)定位到人类1号染色体上。