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Nearest-neighbor non-additivity versus long-range non-additivity in TATA-box structure and its implications for TBP-binding mechanism

机译:TATA盒结构中的近邻非可加性与远程非可加性及其对TBP结合机制的影响

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摘要

TBP recognizes its target sites, TATA boxes, by recognizing their sequence-dependent structure and flexibility. Studying this mode of TATA-box recognition, termed ‘indirect readout’, is important for elucidating the binding mechanism in this system, as well as for developing methods to locate new binding sites in genomic DNA. We determined the binding stability and TBP-induced TATA-box bending for consensus-like TATA boxes. In addition, we calculated the individual information score of all studied sequences. We show that various non-additive effects exist in TATA boxes, dependent on their structural properties. By several criterions, we divide TATA boxes to two main groups. The first group contains sequences with 3–4 consecutive adenines. Sequences in this group have a rigid context-independent cooperative structure, best described by a nearest-neighbor non-additive model. Sequences in the second group have a flexible, context-dependent conformation, which cannot be described by an additive model or by a nearest-neighbor non-additive model. Classifying TATA boxes by these and other structural rules clarifies the different recognition pathways and binding mechanisms used by TBP upon binding to different TATA boxes. We discuss the structural and evolutionary sources of the difficulties in predicting new binding sites by probabilistic weight-matrix methods for proteins in which indirect readout is dominant.
机译:TBP通过识别其序列依赖性结构和灵活性来识别其靶位点TATA盒。研究这种称为“间接读出”的TATA盒识别模式,对于阐明该系统中的结合机制以及开发在基因组DNA中定位新结合位点的方法至关重要。我们确定了共识样TATA盒的结合稳定性和TBP诱导的TATA盒弯曲。另外,我们计算了所有研究序列的个体信息得分。我们证明了TATA盒中存在各种非加性效应,具体取决于它们的结构特性。根据几个标准,我们将TATA框分为两个主要组。第一组包含具有3-4个连续腺嘌呤的序列。该组中的序列具有严格的上下文无关的协作结构,最好由最近邻居非加性模型来描述。第二组中的序列具有灵活的上下文相关构象,无法通过加性模型或最邻近的非加性模型进行描述。通过这些规则和其他结构规则对TATA盒进行分类,可以明确TBP在与不同的TATA盒结合后使用的不同识别途径和结合机制。我们讨论了通过概率权重矩阵方法预测蛋白质的新结合位点的困难的结构和进化来源,其中间接读出占主导地位。

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