Uniting disparate fields to explore transcription factor binding dynamics

描述（由申请人提供）：存储在每个生物的DNA中的信息必须被读取和解释，这主要是由蛋白质完成的。一类调节蛋白控制DNA转录成信使RNA，然后将其翻译成结构蛋白和酶。适当调节转录的能力缺陷是许多人类疾病的基础，其中一些疾病，如癌症和许多与衰老有关的疾病，非常明显地植根于基因组功能障碍。为了参与发育并对环境做出反应，细胞对周围环境的反应非常迅速，部分是通过制定特定的转录反应。因此，转录调控必然是一个基本的动态过程。 然而，我们所知道的关于转录调控机制的几乎所有信息都来自静态分析，如足迹法或染色质免疫沉淀法（ChIP）。这项资助的主要目的是将来自不同学科的联合收割机元素结合起来，以探索体内结合动力学，这是一个在标准ChIP实验中完全丢失的基本参数。我们的目标是（1）测量酵母中几乎每种转录因子的转录因子结合动力学，每个转录因子同时位于基因组的每个位置，（2）在酵母中创建适合FRAP和连续ChIP实验的实验系统，以便我们和其他专家实验室可以在完全相同的系统上使用他们的方法，和（3）测量纯化的转录因子在重建的染色质模板上的靶向和动力学。然后，我们可以使用这些系统来测试特定的假设，染色质组分和转录因子之间的竞争，以测试在调节转录的营业额的生物功能，并确定所需的细胞成分适当调节营业额动态。

DESCRIPTION (provided by applicant): The information stored in the DNA of every living thing must be read and interpreted, and this is accomplished chiefly by proteins. One class of regulatory proteins control the transcription of DNA into messenger RNAs, which are then translated into structural proteins and enzymes. Defects in the ability to properly regulate transcription are at the foundation of many human diseases, with some, such as cancer and many aging-related maladies, very clearly rooted in genomic dysfunction. To take part in development and to respond to their environment, cells respond extremely rapidly to their surroundings, in part by enacting specific transcriptional responses. Therefore transcriptional regulation is by necessity a fundamentally dynamic process. However, almost everything we know about the mechanisms underlying transcriptional regulation are derived from static assays like footprinting or Chromatin Immunoprecipitation (ChIP). The major thrust of this grant is to combine elements from distinct disciplines to explore in vivo binding dynamics, a fundamental parameter that is lost completely in standard ChIP experiments. We aim to (1) measure transcription factor binding dynamics for nearly every transcription factor in yeast, each at every position the genome simultaneously, (2) to create experimental systems in yeast amenable to both FRAP and sequential ChIP experiments, so that we and other expert laboratories can use their methods on the exact same system, and (3) to measure purified transcription factor targeting and dynamics on reconstituted chromatin templates. We can then use these systems to test specific hypotheses regarding competition between chromatin components and transcription factors, to test the biological function of turnover in regulating transcription, and to determine the cellular components required for proper regulation of turnover dynamics.