Characterization of Gradient-Responsive Genetic Programs Using Light Sensors

使用光传感器表征梯度响应遗传程序

• 批准号: 8403398
• 负责人: CHRISTOPHER A VOIGT
• 金额: $ 29.02万
• 依托单位: MASSACHUSETTS INSTITUTE OF TECHNOLOGY
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-01-01 至 2014-12-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8403398
• 关键词: Affect; Algorithms; Binding; Binding Sites; Biological Assay; Biological Models; Biological Phenomena; Cell Communication; Cells; Complex; Computer Simulation; Computing Methodologies; DNA Sequence; Defect; Development; Diffuse; Disease; Embryo; Escherichia coli; Feedback; Free Energy; Gene Expression Profile; Genetic; Genetic Programming; Growth; Kinetics; Lead; Libraries; Light; Location; Logic; Malignant Neoplasms; Measures; Messenger RNA; Methods; Methyl Green; Modeling; Mutation; Neoplasm Metastasis; Neurons; Pattern; Perception; Printing; Process; Property; Regulation; Ribosomes; Shapes; Signal Pathway; Signal Transduction; System; Testing; Thermodynamics; Variant; computerized data processing; design; flexibility; human disease; improved; interest; light intensity; mathematical model; morphogens; programs; public health relevance; sensor; simulation; theories; tool

DESCRIPTION (provided by applicant): Spatial gradients enable cells to precisely organize into complex multicellular patterns. Morphogens are released by clusters of cells and diffuse outward to form a gradient. Surrounding cells convert this gradient into patterns of gene expression using regulatory genetic programs composed of integrated genetic logic, feedback, and cell-cell communication. The central objective of this proposal is to identify the design principles by which genetic programs convert gradients into patterns of gene expression. Our approach will harness two new tools. The first is a set of red and green light sensors that activate a signaling pathway in a graded manner as a function of light intensity. These will be used to deliver light gradients that will be processed as inputs by a genetic program. The second is a suite of computational methods that enable us to convert a desired genetic program into a DNA sequence. This model-guided design allows us to enumerate and evaluate many genetic programs in silico and then construct and experimentally test a library of the most interesting programs. Further, a biophysical method that predicatively tunes expression levels by changing the ribosome binding site sequence will be harnessed to quantitatively compare the mutational robustness and evolvability of programs. The Aims are organized around the testing of hypotheses as to how regulatory networks process single and multiple gradient signals. Specifically, we will test the following theories: (i) Embedded feedforward loops improve robustness to mutations that affect expression levels (Aim 1). (ii) Feedback loops and spatial bistability increase pattern sharpness and robustness (Aim 1). (iii) Programs that integrate opposing gradients have improved robustness and pattern evolvability (Aim 2). (iv) Opposing gradients can be used as part of size-independent center-finding algorithms (Aim 2). The use of synthetic genetic circuits and E. coli as a model system will make it possible to characterize the gradient-processing properties of many genetic programs and make quantitative comparisons to a fully parameterized mathematical model. This approach will elucidate principles of how regulatory networks are organized to process gradients that can then be generalized to other systems.

描述(申请人提供)：空间梯度使细胞能够精确地组织成复杂的多细胞模式。形态原由成团的细胞释放，并向外扩散形成梯度。周围的细胞利用由整合的遗传逻辑、反馈和细胞间交流组成的调控遗传程序，将这种梯度转化为基因表达的模式。这项提案的中心目标是确定遗传程序将梯度转换为基因表达模式的设计原则。我们的方法将利用两个新工具。第一个是一组红光和绿光传感器，它们以分级的方式激活信号通路，作为光强度的函数。这些将被用来传递光梯度，这些光梯度将作为遗传程序的输入进行处理。第二种是一套计算方法，使我们能够将所需的遗传程序转换为DNA序列。这种以模型为导向的设计使我们能够列举和评估Silico中的许多遗传程序，然后构建和实验测试最有趣的程序库。此外，将利用一种通过改变核糖体结合位点序列来预测调节表达水平的生物物理方法来定量比较程序的突变稳健性和进化性。这些目标围绕有关监管网络如何处理单一和多个梯度信号的假设进行测试。具体地说，我们将测试以下理论：(I)嵌入的前馈循环提高了对影响表达水平的突变的稳健性(目标1)。(2)反馈回路和空间双稳态提高了模式的清晰度和稳健性(目标1)。(3)整合相反梯度的程序具有更好的稳健性和模式可演化性(目标2)。(4)相反的梯度可用作与大小无关的中心寻找算法的一部分(目标2)。使用合成遗传电路和大肠杆菌作为模型系统，将有可能表征许多遗传程序的梯度处理特性，并与完全参数化的数学模型进行定量比较。这种方法将阐明如何组织监管网络以处理梯度的原则，然后这些梯度可以推广到其他系统。