Discovering gene regulatory networks through combination of diverse large-scale biological evidence

通过结合多种大规模生物证据发现基因调控网络

• 批准号: 402087-2011
• 负责人: PeñaCastillo, Lourdes
• 金额: $ 1.38万
• 依托单位: Memorial University of Newfoundland
• 依托单位国家: 加拿大
• 项目类别: Discovery Grants Program - Individual
• 财政年份: 2017
• 资助国家: 加拿大
• 起止时间: 2017-01-01 至 2018-12-31
• 项目状态: 已结题
• 来源: https://www.nserc-crsng.gc.ca/ase-oro/Details-Detailles_eng.asp?id=635112
• 关键词: Discovering; gene; regulatory; networks; through

A major challenge in current post-genome molecular biology and bioinformatics research is to fully understand gene regulation: how and when each and every gene is switched on and off during the life of the cell, particularly in response to changing environmental or cellular states. Gene regulation is essential to organism survival, and deciphering how genes are regulated is critical for understanding genetic misregulation, a major cause of disease and developmental malformations. Deciphering gene regulation is a reverse-engineering problem. The goal is to understand how a system (in this case the cell) works from experimental evidence. To this end, biologists disturb the inputs (changes in the environment or genetic alterations) and monitor the outputs (for example, measurements of relative abundance of genes in the cell). Distinct measurements of the outputs represent aspects of the same regulatory mechanism and can be combined to formulate accurate models of gene regulation. These models are usually called gene regulatory or transcriptional networks. Computational approaches can take advantage of the wealth of biological information that is being generated and investigate the general principles of gene regulation. Development of computational approaches capable of doing this is a very active and promising area of research. The main goal of this proposal is to develop a novel machine learning system that combines diverse recently-generated biological evidence to infer transcriptional networks. Expected outcomes associated with this research program are: 1) to improve our understanding of how cells control gene expression, which plays a key role in human disease; 2) to uncover previously unknown regulatory interactions; 3) to develop an enabling technology for biologists to further analyze their own data; and 4) to develop novel computer programs to model gene regulation. This research program will also train graduate students in the interdisciplinary area of bioinformatics. The research results will be of interest to researchers in bioinformatics, computer science and biology, and as an enabling technology for biologists our system will have a large impact in the molecular biology research community in Canada and abroad.

当前后基因组分子生物学和生物信息学研究的一个主要挑战是充分理解基因调控：在细胞的生命过程中，每个基因是如何以及何时打开和关闭的，特别是在应对不断变化的环境或细胞状态时。基因调控对生物体的生存至关重要，而破译基因是如何调控的对于理解遗传失调是至关重要的，遗传失调是疾病和发育畸形的主要原因。破解基因调控是一个逆向工程问题。目标是从实验证据中了解系统（在这种情况下是细胞）如何工作。为此，生物学家干扰输入（环境或遗传改变的变化）并监测输出（例如，测量细胞中基因的相对丰度）。输出的不同测量值代表了相同调控机制的各个方面，并且可以结合起来制定精确的基因调控模型。这些模型通常被称为基因调控或转录网络。计算方法可以利用正在生成的丰富的生物信息，并研究基因调控的一般原理。能够做到这一点的计算方法的发展是一个非常活跃和有前途的研究领域。该提案的主要目标是开发一种新的机器学习系统，该系统结合了各种最近生成的生物证据来推断转录网络。与这项研究计划相关的预期成果是：1）提高我们对细胞如何控制基因表达的理解，这在人类疾病中起着关键作用; 2）发现以前未知的调控相互作用; 3）开发一种使生物学家能够进一步分析自己数据的技术; 4）开发新的计算机程序来模拟基因调控。该研究计划还将培养生物信息学跨学科领域的研究生。研究结果将是感兴趣的研究人员在生物信息学，计算机科学和生物学，并作为一个使能技术的生物学家，我们的系统将有很大的影响，在分子生物学研究界在加拿大和国外。