TenHarmsel A, Biggin M D
Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, Connecticut 06520-8114, USA.
Mol Cell Biol. 1995 Oct;15(10):5492-8. doi: 10.1128/MCB.15.10.5492.
Previous studies indicated that repression by eve involves cooperative DNA binding and leads to the formation of a DNA loop which encompasses the DNA sequences normally bound by the RNA polymerase II general transcription factors. To test the general principle of whether bending of a basal promoter sequence can contribute directly to repression of transcription, a minicircle template of 245 bp was used. In a purified transcription system, transcription from the minicircular DNA is greatly reduced compared with that from the identical DNA fragment in linear form. Transcription is also reduced when the minicircle contains a single-stranded nick, indicating that transcription is reduced because of DNA bending, rather than any constraint on supercoiling. We show that the reduced transcription from the minicircle in these experiments is not due to a reduced rate of elongation by RNA polymerase II. Rather, repression occurs, at least in part, because binding of the general transcription factor TFIID to the minicircle is strongly inhibited compared with binding to the linear DNA. We suggest that bending DNA may be a mechanism by which eukaryotic transcription may be regulated, by modulating the activity of the general transcription factors.
先前的研究表明,eve介导的基因抑制涉及协同DNA结合,并导致形成一个DNA环,该环包含通常由RNA聚合酶II通用转录因子结合的DNA序列。为了验证基础启动子序列的弯曲是否能直接导致转录抑制这一普遍原理,使用了一个245 bp的小环模板。在一个纯化的转录系统中,与线性形式的相同DNA片段相比,小环DNA的转录大幅减少。当小环含有一个单链切口时,转录也会减少,这表明转录减少是由于DNA弯曲,而不是对超螺旋的任何限制。我们表明,在这些实验中,小环转录减少并非由于RNA聚合酶II的延伸速率降低。相反,抑制至少部分是因为与线性DNA相比,通用转录因子TFIID与小环的结合受到强烈抑制。我们认为,弯曲DNA可能是一种通过调节通用转录因子的活性来调控真核生物转录的机制。