Hochhuth C, Doenecke D
Institute of Biochemistry and Molecular Cell Biology, Georg-August-Universität Göttingen, Germany.
J Cell Biochem. 1992 Nov;50(3):316-23. doi: 10.1002/jcb.240500312.
The expression of the human H1 zero histone gene and of a main type H1 gene was analyzed in two human leukemia cell lines. The main type, replication dependent H1 gene expression reflected the state of proliferation of both cell lines. No H1 zero mRNA was detected in the promyelocytic HL-60 line, whereas the monocytic U937 cells showed low steady-state levels of 1H zero mRNA. Stimulation of HL-60 with several known inducers of differentiation failed to induce any accumulation of H1 zero mRNA. Treatment of U937 with phorbol ester or butyrate, on the other hand, led to an increase of the H1 zero mRNA concentration.
在两个人类白血病细胞系中分析了人类H1零组蛋白基因和一种主要类型H1基因的表达情况。主要类型的、依赖复制的H1基因表达反映了两个细胞系的增殖状态。在早幼粒细胞HL-60系中未检测到H1零mRNA,而单核细胞U937细胞显示出低稳态水平的H1零mRNA。用几种已知的分化诱导剂刺激HL-60未能诱导H1零mRNA的任何积累。另一方面,用佛波酯或丁酸盐处理U937导致H1零mRNA浓度增加。