Pauza C D
Mol Cell Biol. 1987 Jan;7(1):342-8. doi: 10.1128/mcb.7.1.342-348.1987.
Antigen-stimulated human T lymphocytes must bind the immunoregulatory hormone interleukin 2 (IL-2) if they are to transit from the G1 to the S phase of the cell cycle. Indirect methods, such as the measurement of thymidine uptake rates, were previously the only means available for exploring the mechanism of action of IL-2. Several cDNA clones have been isolated which are expressed subsequent to IL-2 binding, and the expression of two of these genes. Tact52 and Tact75, is regulated directly at the level of transcription; expression of the proto-oncogene c-myb is also regulated directly by IL-2 binding. These genes thus constitute a set which is coordinately regulated in the course of the transition from G1 to S phase of human T lymphocytes, and their expression depends on IL-2 binding.
抗原刺激的人类T淋巴细胞若要从细胞周期的G1期过渡到S期,就必须结合免疫调节激素白细胞介素2(IL-2)。间接方法,如测量胸腺嘧啶核苷摄取率,以前是探索IL-2作用机制的唯一可用手段。已经分离出几个在IL-2结合后表达的cDNA克隆,其中两个基因Tact52和Tact75的表达在转录水平受到直接调控;原癌基因c-myb的表达也受到IL-2结合的直接调控。因此,这些基因构成了一组在人类T淋巴细胞从G1期过渡到S期的过程中受到协同调控的基因,它们的表达依赖于IL-2结合。