Devlin C, Tice-Baldwin K, Shore D, Arndt K T
Cold Spring Harbor Laboratory, New York 11724.
Mol Cell Biol. 1991 Jul;11(7):3642-51. doi: 10.1128/mcb.11.7.3642-3651.1991.
The major in vitro binding activity to the Saccharomyces cerevisiae HIS4 promoter is due to the RAP1 protein. In the absence of GCN4, BAS1, and BAS2, the RAP1 protein binds to the HIS4 promoter in vivo but cannot efficiently stimulate HIS4 transcription. RAP1, which binds adjacently to BAS2 on the HIS4 promoter, is required for BAS1/BAS2-dependent activation of HIS4 basal-level transcription. In addition, the RAP1-binding site overlaps with the single high-affinity HIS4 GCN4-binding site. Even though RAP1 and GCN4 bind competitively in vitro, RAP1 is required in vivo for (i) the normal steady-state levels of GCN4-dependent HIS4 transcription under nonstarvation conditions and (ii) the rapid increase in GCN4-dependent steady-state HIS4 mRNA levels following amino acid starvation. The presence of the RAP1-binding site in the HIS4 promoter causes a dramatic increase in the micrococcal nuclease sensitivity of two adjacent regions within HIS4 chromatin: one region contains the high-affinity GCN4-binding site, and the other region contains the BAS1- and BAS2-binding sites. These results suggest that RAP1 functions at HIS4 by increasing the accessibility of GCN4, BAS1, and BAS2 to their respective binding sites when these sites are present within chromatin.
对酿酒酵母HIS4启动子的主要体外结合活性归因于RAP1蛋白。在缺乏GCN4、BAS1和BAS2的情况下,RAP1蛋白在体内与HIS4启动子结合,但不能有效刺激HIS4转录。RAP1在HIS4启动子上与BAS2相邻结合,是BAS1/BAS2依赖的HIS4基础水平转录激活所必需的。此外,RAP1结合位点与单个高亲和力的HIS4 GCN4结合位点重叠。尽管RAP1和GCN4在体外竞争性结合,但在体内,RAP1对于(i)非饥饿条件下GCN4依赖的HIS4转录的正常稳态水平以及(ii)氨基酸饥饿后GCN4依赖的稳态HIS4 mRNA水平的快速增加是必需的。HIS4启动子中RAP1结合位点的存在导致HIS4染色质内两个相邻区域的微球菌核酸酶敏感性显著增加:一个区域包含高亲和力的GCN4结合位点,另一个区域包含BAS1和BAS2结合位点。这些结果表明,当这些位点存在于染色质中时,RAP1通过增加GCN4、BAS1和BAS2对其各自结合位点的可及性在HIS4发挥作用。