Turcotte B, Guertin M, Chevrette M, LaRue H, Bélanger L
Nucleic Acids Res. 1986 Dec 22;14(24):9827-41. doi: 10.1093/nar/14.24.9827.
Three major regions of DNase I hypersensitivity (DH) were found in alpha 1-fetoprotein (AFP) chromatin of rat liver. DH site I is located at the transcription initiation site and associated with ongoing AFP transcription. DH site II is located 2.5 kb upstream from the cap site: it is developmental stage-dependent but dissociable from ongoing AFP transcription. DH site III, 3.7 kb upstream from the cap site, behaves as hepatocyte-constitutive. DH sites are present in similar regions of liver albumin chromatin. Dexamethasone-induced AFP gene repression is accompanied by the selective loss of AFP DH site I, a likely result of glucocorticoid receptors binding to a DNA recognition sequence located 5'-adjacent to DH site I. Sl nuclease-hypersensitive sites were found on naked superhelical AFP and albumin DNA, but do not appear to contribute DH sites in liver chromatin. The extent of hypomethylation of HpaII sites at the 5'-end of the AFP gene correlates positively with the level of potential and actual expression of the gene. We conclude that developmental and hormonal regulation of the AFP gene is confined within congruent to 4 kb of 5'-flanking DNA, and we discuss possible hierarchical interactions among DH sites, in relation to DNA methylation and replication.
在大鼠肝脏甲胎蛋白(AFP)染色质中发现了三个主要的脱氧核糖核酸酶I超敏(DH)区域。DH位点I位于转录起始位点,与正在进行的AFP转录相关。DH位点II位于帽位点上游2.5 kb处:它依赖于发育阶段,但与正在进行的AFP转录可分离。DH位点III位于帽位点上游3.7 kb处,表现为肝细胞组成型。肝脏白蛋白染色质的相似区域也存在DH位点。地塞米松诱导的AFP基因抑制伴随着AFP DH位点I的选择性丧失,这可能是糖皮质激素受体与位于DH位点I 5'相邻的DNA识别序列结合的结果。在裸露的超螺旋AFP和白蛋白DNA上发现了单链核酸酶超敏位点,但它们似乎对肝脏染色质中的DH位点没有贡献。AFP基因5'端HpaII位点的低甲基化程度与该基因潜在和实际表达水平呈正相关。我们得出结论,AFP基因的发育和激素调节局限于5'侧翼DNA的4 kb范围内,并且我们讨论了DH位点之间可能的层级相互作用,以及与DNA甲基化和复制的关系。