Quantitative regulatory genomics: networks, cis-regulatory codes, and phenotypic variation

定量调控基因组学：网络、顺式调控密码和表型变异

• 批准号: 10267176
• 负责人: Saurabh Sinha
• 金额: $ 35.7万
• 依托单位: UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN
• 依托单位国家: 美国
• 财政年份: 2019
• 资助国家: 美国
• 起止时间: 2019-09-20 至 2024-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/10267176
• 关键词: Antineoplastic Agents; Behavioral; Binding Sites; Biological; Biological Assay; Biology; Cell Line; Cell physiology; Chromatin; Code; Collaborations; Computing Methodologies; Cytotoxic agent; DNA; DNA Sequence; Data; Embryonic Development; Estrogens; Exhibits; Foundations; Gene Expression; Genes; Genetic Polymorphism; Genetic Transcription; Genomics; Genotype; Goals; Individual; Inflammation; Investigation; Knowledge; Link; Logic; Malignant Neoplasms; Methods; Modeling; Modernization; Molecular; Multiomic Data; Patients; Pharmaceutical Preparations; Pharmacogenomics; Phenotype; Property; Regulator Genes; Reporter; Research; Shapes; Statistical Models; Techniques; Transcriptional Regulation; Untranslated RNA; Variant; Work; base; behavioral response; biophysical model; gene interaction; genomic data; insight; machine learning method; malignant breast neoplasm; neurogenomics; programs; reconstruction; response; social; synergism; tool; transcription factor; transcriptomics

How do changes in DNA sequence impact organismal properties? This is a central question of modern biology, and insights into it can help us understand, among other things, why patients respond differently to the same treatment, or why some species exhibit behavioral properties not seen in other species. A major hurdle in solving this ‘genotype-to-phenotype’ problem is our poor knowledge of gene regulatory mechanisms underlying phenotypes and cellular processes, and how those mechanisms are encoded in DNA. It also leads to severe difficulties in prioritizing phenotype-linked non-coding variants (polymorphisms) for further investigation. Driven by these challenges, my lab seeks to develop quantitative frameworks for describing and discovering transcriptional regulatory mechanisms. We have made significant progress towards this goal in two main directions: (1) We have developed detailed biophysical models of the cis-regulatory encoding of gene expression. Using these models we have shown how the regulatory function of transcription factor (TF) binding sites depends on their sequence and DNA shape, as well as their ‘trans-context’, e.g., cellular concentrations of regulators, and ‘cis-context’, e.g., proximity to other TF binding sites and chromatin states. (2) We have devised statistical models to discover TF-gene interactions from transcriptomic data, as well as other types of ‘omics’ data if available. Working closely with biologists, we have applied these models to understand phenotypes such as cytotoxic drug response in cell lines, behavioral response to social encounters, and embryonic development. Building on the strong foundations of our past work, I propose to establish a research program that studies transcriptional regulation holistically at the cis- and trans- levels. Our new pursuits will include: (1) use of our computational, sequence-level models to describe two data-rich mammalian regulatory programs, an experimental collaboration to dissect the cis-regulatory logic of a key inflammation gene using massively parallel reporter assays, and major advances in our modeling techniques; (2) new machine learning methods for reconstructing networks of TF-gene interactions that explain phenotypic differences, integration of cis- and trans-regulatory evidence from multi-omics data, and collaborations to apply these methods in cancer pharmacogenomics and behavioral neurogenomics; (3) a new probabilistic framework to combine traditional statistical scores of a non-coding variant with quantitative predictions of its regulatory impact based on the above-mentioned techniques. Explorations of new forms of synergy among these related goals of network reconstruction, cis-regulatory sequence modeling and variant interpretation will be woven throughout our research program.

DNA序列的变化如何影响生物体特性？这是现代社会的一个中心问题