Cress W D, Nevins J R
Department of Genetics, Howard Hughes Medical Institute, Duke University Medical Center, Durham, North Carolina 27710, USA.
Mol Cell Biol. 1996 May;16(5):2119-27. doi: 10.1128/MCB.16.5.2119.
We examined the role of promoter architecture, as well as that of the DNA-bending capacity of the E2F transcription factor family, in the activation of transcription. DNA phasing analysis revealed that a consensus E2F site in the E2F1 promoter possesses an inherent bend with a net magnitude of 40 +/-2 degrees and with an orientation toward the major groove relative to the center of the E2F site. The inherent DNA bend is reversed upon binding of E2F, generating a net bend with a magnitude of 25 +/- 3 degrees oriented toward the minor groove relative to the center of the E2F site. We also found that three members of the E2F family, in conjunction with the DP1 protein, bend the DNA toward the minor groove, suggesting that DNA bending is a characteristic of the entire E2F family. The Rb-E2F complex, on the other hand, does not reverse the intrinsic DNA bend. Analysis of a series of E2F1 deletion mutants defined E2F1 sequences which are not required for DNA binding but are necessary for the DNA-bending capacity of E2F. An internal region of E2F1, previously termed the marked box, which is highly homologous among E2F family members, was particularly important in DNA bending. We also found that a bent DNA structure can be a contributory component in the activation of the E2F1 promoter but is not critical in the repression of that promoter in quiescent cells. This finding suggests that E2F exhibits characteristics typical of modular transcription factors, with independent DNA-binding and transcriptional activation functions, but also has features of architectural factors that alter DNA structure.
我们研究了启动子结构以及E2F转录因子家族的DNA弯曲能力在转录激活中的作用。DNA定相分析表明,E2F1启动子中的共有E2F位点具有固有的弯曲,净弯曲幅度为40±2度,相对于E2F位点中心朝向大沟。E2F结合后,固有的DNA弯曲方向反转,产生相对于E2F位点中心朝向小沟的净弯曲,幅度为25±3度。我们还发现,E2F家族的三个成员与DP1蛋白一起,使DNA向小沟弯曲,这表明DNA弯曲是整个E2F家族的特征。另一方面,Rb-E2F复合物不会反转内在的DNA弯曲。对一系列E2F1缺失突变体的分析确定了E2F1中对于DNA结合不是必需的但对于E2F的DNA弯曲能力是必需的序列。E2F1的一个内部区域,以前称为标记框,在E2F家族成员中高度同源,在DNA弯曲中尤为重要。我们还发现,弯曲的DNA结构可能是E2F1启动子激活的一个促成因素,但在静止细胞中对该启动子的抑制并不关键。这一发现表明,E2F表现出模块化转录因子的典型特征,具有独立的DNA结合和转录激活功能,但也具有改变DNA结构的结构因子的特征。