Traditionally, disease causal mutations were thought to disrupt gene function. However, it becomes more and more clear that many deleterious mutations could exhibit a 'gain-of-function' behavior. Systematic investigation of such mutations has been lacking and largely overlooked. In the last few years it has become more clear that the efficacy and specificity of signal transduction in a cell is, at heart, a problem of molecular recognition and protein interaction. In distinct cell types (with varying genotypes), precise signal transduction controls cell decision, including gene regulation and phenotypic output. When signal transduction goes awry due to gain-of- function mutations, it would give rise to various disease types. Research in my laboratory is focused on developing and utilizing quantitative and molecular technologies to understand protein interaction networks and their perturbations by genomic mutations, bridging genotype and phenotype in health and disease. Our overall goal is to contribute to the understanding of disease mechanisms and of more open ended questions about explanations for 'missing heritability' in genome-wide association studies. We envision that It will be instrumental to push current human genetics research paradigm towards a thorough functional and quantitative modeling of all genomic mutations and their mechanistic molecular interaction events involved in disease development and progression. Therefore, gaining a systems-level understanding of gain-of-function mutations requires to resolve the plastic nature of molecular interactions, and to integrate experimental and computational strategies at the genome scale. Many fundamental questions pertaining to genotype-phenotype relationships remain unresolved. For example, how do interaction networks undergo rewiring upon gain-of- function mutations? Which mutations are key for gene regulation and cellular decisions? Do mutagtions exhit allel-specific behaviors or how do the allelic combinations work to coordinate cellular phenotypes? Is it possible to leverage molecular interaction networks to engineer signal transduction in cells, aiming to cure disease? To begin to address these questions, in this proposal, we will systematically interrogate of gain-of-function disease mutations using a novel network-based systems biology framework. We will then decipher condition-dependent protein-protein interaction perturbations induced by gain-of-function mutations in disorder regions and phosphorylation sites. Finally, we will determine allele-specific and allele-combinatorial effect of gain-of-function mutations on protein interaction network rewiring. Together, this integrative proposal is innovative because it will provide insights in prioritizing driver functional gain-of-function disease mutations, and uncovering individualized molecular mechanisms at a base resolution. Furthermore, it is significant because it will greatly facilitate the functional annotation of a large number of gain-of-function mutations, providing a fundamental link between genotype and phenotype in general human disease.

Public Health Relevance

Although disease causal mutations were traditionally thought to disrupt gene function, it becomes increasingly appreciated that many deleterious mutations could exhibit a 'gain-of-function' behavior. Current knowledge and technologies that could identify such mutations and their functional consequences across diverse human diseases are fragmentary and extremely limited, and have been gleaned entirely from a handful of pathological examples. This proposal describes a set of innovative projects to broadly discover and characterize gain-of-function genomic aberrations that influence protein activities that regulate information flow in cellular signaling networks, and lessons learned will provide much needed insight into disease mechanisms and how they can be modulated for therapeutic benefit.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Unknown (R35)
Project #
5R35GM133658-02
Application #
10017306
Study Section
Special Emphasis Panel (ZGM1)
Program Officer
Krasnewich, Donna M
Project Start
2019-09-15
Project End
2024-08-31
Budget Start
2020-09-01
Budget End
2021-08-31
Support Year
2
Fiscal Year
2020
Total Cost
Indirect Cost
Name
University of Texas Austin
Department
Neurology
Type
Schools of Medicine
DUNS #
170230239
City
Austin
State
TX
Country
United States
Zip Code
78759