van Wijnen A J, Lian J B, Stein J L, Stein G S
Department of Cell Biology, University of Massachusetts Medical Center, Worcester 01655.
J Cell Biochem. 1991 Dec;47(4):337-51. doi: 10.1002/jcb.240470408.
Protein/DNA interactions of the H3-ST519 histone gene promoter were analyzed in vitro. Using several assays for sequence specificity, we established binding sites for ATF/AP1-, CCAAT-, and HiNF-D related DNA binding proteins. These binding sites correlate with two genomic protein/DNA interaction domains previously established for this gene. We show that each of these protein/DNA interactions has a counterpart in other histone genes: H3-ST519 and H4-F0108 histone genes interact with ATF- and HiNF-D related binding activities, whereas H3-ST519 and H1-FNC16 histone genes interact with the same CCAAT-box binding activity. These factors may function in regulatory coupling of the expression of different histone gene classes. We discuss these results within the context of established and putative protein/DNA interaction sites in mammalian histone genes. This model suggests that heterogeneous permutations of protein/DNA interaction elements, which involve both general and cell cycle regulated DNA binding proteins, may govern the cellular competency to express and coordinately control multiple distinct histone genes.
在体外分析了H3-ST519组蛋白基因启动子的蛋白质/DNA相互作用。通过几种序列特异性分析方法,我们确定了与ATF/AP1、CCAAT和HiNF-D相关的DNA结合蛋白的结合位点。这些结合位点与先前为该基因确定的两个基因组蛋白质/DNA相互作用结构域相关。我们发现这些蛋白质/DNA相互作用中的每一种在其他组蛋白基因中都有对应物:H3-ST519和H4-F0108组蛋白基因与ATF和HiNF-D相关的结合活性相互作用,而H3-ST519和H1-FNC16组蛋白基因与相同的CCAAT框结合活性相互作用。这些因子可能在不同组蛋白基因类别的表达调控偶联中发挥作用。我们在哺乳动物组蛋白基因中已确定和推测的蛋白质/DNA相互作用位点的背景下讨论了这些结果。该模型表明,蛋白质/DNA相互作用元件的异质排列,涉及一般和细胞周期调控的DNA结合蛋白,可能决定细胞表达和协调控制多个不同组蛋白基因的能力。