Shiels A, Marashi F, Stein G, Stein J
Biochem Biophys Res Commun. 1985 Feb 28;127(1):239-46. doi: 10.1016/s0006-291x(85)80150-9.
Cultured mammalian cells were transfected with a recombinant human H4 histone gene. S1 nuclease mapping of cellular RNAs from transfected cells revealed: (i) correct initiation of transcription at the cap site, with some transcripts originating from other sites in the 5' flanking region of this H4 gene; (ii) cis-linkage of an SV-40 transcriptional enhancer element upstream of the H4 5'-flanking region resulted in about a 50-fold increase in the level of correctly initiated H4 mRNA and (iii) in a heterologous murine system stability of human H4 mRNAs was apparently sensitive to inhibition of DNA-synthesis by hydroxyurea. Our results suggest that certain sequences required for the initiation of a human H4 histone gene transcript reside within the 210 nucleotides immediately upstream from the cap site and that the level of expression is influenced by the introduction of an enhancer element.
用重组人H4组蛋白基因转染培养的哺乳动物细胞。对来自转染细胞的细胞RNA进行S1核酸酶图谱分析显示:(i)在帽位点转录正确起始,一些转录本起源于该H4基因5'侧翼区域的其他位点;(ii)H4 5'侧翼区域上游的SV-40转录增强子元件的顺式连接导致正确起始的H4 mRNA水平增加约50倍;(iii)在异源小鼠系统中,人H4 mRNA的稳定性显然对羟基脲抑制DNA合成敏感。我们的结果表明,人H4组蛋白基因转录起始所需的某些序列位于帽位点上游紧邻的210个核苷酸内,并且表达水平受增强子元件引入的影响。