Quitschke W W, Taheny M J, Fochtmann L J, Vostrov A A
Department of Psychiatry and Behavioral Science, State University of New York at Stony Brook, Stony Brook, NY 11794-8101, USA.
Nucleic Acids Res. 2000 Sep 1;28(17):3370-8. doi: 10.1093/nar/28.17.3370.
High levels of transcription from the amyloid precursor protein promoter are dependent on the binding of CTCF to the APBbeta core recognition sequence located between positions -82 and -93 upstream from the transcriptional start site. CTCF comprises 727 amino acids and contains 11 zinc finger motifs arranged in tandem that are flanked by 267 amino acids on the N-terminal side and 150 amino acids on the C-terminal side. Deletion of either the N- or the C-terminal regions outside of the zinc finger domain had no detrimental effect on the binding of CTCF to APBbeta. However, internal deletions of zinc fingers 5-7 completely abolished binding. The binding of full-length CTCF generated a DNase I protected domain extending from position -78 to -116, which was interrupted by a hypersensitive site at position -99. Selective deletions from the N- and C-terminal sides of the zinc finger domain showed that the N-terminal end of the zinc finger domain was aligned toward the transcriptional start site. Furthermore, deletions of zinc fingers peripheral to the essential zinc fingers 5-7 decreased the stability of the binding complex by interrupting sequence-specific interactions.
淀粉样前体蛋白启动子的高水平转录依赖于CTCF与位于转录起始位点上游-82至-93位之间的APBβ核心识别序列的结合。CTCF由727个氨基酸组成,包含11个串联排列的锌指基序,其N端侧翼为267个氨基酸,C端侧翼为150个氨基酸。锌指结构域外的N端或C端区域的缺失对CTCF与APBβ的结合没有不利影响。然而,锌指5-7的内部缺失完全消除了结合。全长CTCF的结合产生了一个从-78位延伸至-116位的DNase I保护结构域,该结构域在-99位被一个超敏位点中断。从锌指结构域的N端和C端进行选择性缺失表明,锌指结构域的N端朝向转录起始位点排列。此外,基本锌指5-7外围的锌指缺失通过中断序列特异性相互作用降低了结合复合物的稳定性。