Green L, Stein G, Stein J
Mol Cell Biochem. 1984;60(2):123-30. doi: 10.1007/BF00222482.
The cellular abundance of H2A, H2B, H3 and H4 histone mRNA sequences was determined prior to and at various times after stimulation of non-dividing human diploid fibroblasts to proliferate. The representation of histone mRNAs was quantitated by electrophoretic fractionation of total cellular RNAs, diffusion transfer to nitrocellulose and hybridization with a series of cloned genomic human histone sequences. The levels of mRNAs for the four core histones were observed to be temporally and quantitatively coupled with both DNA replication and histone protein synthesis. Therefore, a contribution to the regulation of histone gene expression at a transcriptional level is suggested.
在刺激非分裂的人二倍体成纤维细胞进行增殖之前及之后的不同时间,测定了H2A、H2B、H3和H4组蛋白mRNA序列的细胞丰度。通过对总细胞RNA进行电泳分离、扩散转移至硝酸纤维素膜并与一系列克隆的基因组人组蛋白序列杂交,对组蛋白mRNA的表达量进行定量。观察到四种核心组蛋白的mRNA水平在时间和数量上与DNA复制及组蛋白蛋白质合成均相关联。因此,提示在转录水平对组蛋白基因表达存在调控作用。