Plumb M, Marashi F, Green L, Zimmerman A, Zimmerman S, Stein J, Stein G
Proc Natl Acad Sci U S A. 1984 Jan;81(2):434-8. doi: 10.1073/pnas.81.2.434.
A cloned genomic DNA fragment containing a human histone H1 gene has been used to analyze histone H1 gene expression in two human cell lines (HeLa S3 and WI-38). The cellular abundance of histone H1 mRNA was compared with that of core (H2A, H2B, H3, and H4) histone mRNAs as a function of the cell cycle: core and H1 histone mRNA levels are related both to each other and to the apparent rate of DNA synthesis and are rapidly destabilized after DNA synthesis inhibition. The use of three synchronization protocols, and of transformed and normal diploid cells in culture, suggests that the detected core and H1 histone mRNA levels are regulated by similar mechanisms in continuously dividing human cell lines and nondividing cells stimulated to proliferate.
一个包含人类组蛋白H1基因的克隆基因组DNA片段已被用于分析两种人类细胞系(HeLa S3和WI-38)中的组蛋白H1基因表达。作为细胞周期的函数,将组蛋白H1 mRNA的细胞丰度与核心组蛋白(H2A、H2B、H3和H4)的mRNA丰度进行了比较:核心组蛋白和H1组蛋白的mRNA水平相互关联,并且与DNA合成的表观速率相关,在DNA合成抑制后迅速不稳定。使用三种同步化方案以及培养中的转化细胞和正常二倍体细胞表明,在持续分裂的人类细胞系和被刺激增殖的非分裂细胞中,检测到的核心组蛋白和H1组蛋白的mRNA水平受相似机制调控。