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顺式调控模块中协同转录激活的距离和螺旋相位依赖性。

Distance and helical phase dependence of synergistic transcription activation in cis-regulatory module.

机构信息

The State Key Laboratory of Pharmaceutical Biotechnology and Affiliated Stomatological Hospital, Nanjing University, Nanjing, People's Republic of China.

出版信息

PLoS One. 2012;7(1):e31198. doi: 10.1371/journal.pone.0031198. Epub 2012 Jan 27.

Abstract

Deciphering of the spatial and stereospecific constraints on synergistic transcription activation mediated between activators bound to cis-regulatory elements is important for understanding gene regulation and remains largely unknown. It has been commonly believed that two activators will activate transcription most effectively when they are bound on the same face of DNA double helix and within a boundary distance from the transcription initiation complex attached to the TATA box. In this work, we studied the spatial and stereospecific constraints on activation by multiple copies of bound model activators using a series of engineered relative distances and stereospecific orientations. We observed that multiple copies of the activators GAL4-VP16 and ZEBRA bound to engineered promoters activated transcription more effectively when bound on opposite faces of the DNA double helix. This phenomenon was not affected by the spatial relationship between the proximal activator and initiation complex. To explain these results, we proposed the novel concentration field model, which posits the effective concentration of bound activators, and therefore the transcription activation potential, is affected by their stereospecific positioning. These results could be used to understand synergistic transcription activation anew and to aid the development of predictive models for the identification of cis-regulatory elements.

摘要

解析结合于顺式调控元件的激活子之间协同转录激活的空间和立体专一性限制对于理解基因调控非常重要,但目前仍知之甚少。人们普遍认为,当两个激活子结合在 DNA 双螺旋的同一面上并且与附着在 TATA 盒上的转录起始复合物的距离在一定范围内时,它们将最有效地激活转录。在这项工作中,我们使用一系列工程化的相对距离和立体专一性取向研究了多个结合的模型激活子对激活的空间和立体专一性限制。我们观察到,结合于工程化启动子上的多个 GAL4-VP16 和 ZEBRA 激活子结合在 DNA 双螺旋的相反面上时,能更有效地激活转录。这种现象不受近端激活子与起始复合物之间空间关系的影响。为了解释这些结果,我们提出了新颖的浓度场模型,该模型假设结合激活子的有效浓度,因此转录激活潜能受其立体专一性定位的影响。这些结果可用于重新理解协同转录激活,并有助于开发用于识别顺式调控元件的预测模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a09/3267773/7c468cf33584/pone.0031198.g001.jpg

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