Cells and organisms, from simple to complex, carry the same genetic DNA sequence organized into genes. Multicellular eukaryotes transcribe and process genes into RNA isoforms through a process called alternative splicing. Alternative splicing is developmentally and cell-type specifically regulated. It is foundational to how higher organisms? genomes are decoded. Yet, critical and fundamental questions regarding its regulation and the function of its output remain unanswered. For example, circRNA being a ubiquitous product of alternative splicing was only discovered in 2012, and its regulation and function remains enigmatic. circRNAs? discovery revealed a larger critical knowledge gap in the field for ?what, how and why? genes are alternatively spliced. What RNA splice variants are expressed, how splicing is regulated and which spliced RNAs have essential functions? Answering these questions is critical for predicting which of myriad genetic variants cause disease and why they do so. Answers will also enable a new generation of digital nucleic acid biomarkers and diagnostics for disease, drug targets for correcting dysregulated splicing and identification of pathogenic protein- or non-coding products (respectively) as well as fundamental basic scientific insight into evolution and function of eukaryotic genomes. The proposed research will couple novel statistical analyses of -omics data by taking an unbiased approach and including biological features that are understudied or un-annotated. Predictions will be coupled with incisive experimental validation to reveal new principles of how RNAs, including circRNAs, are spliced and how they function. This research potentiates significant new discoveries in why alternative splicing exists and how this understanding can be used for precision medicine.

Public Health Relevance

(Public Health Relevance) All cells in an organism share the same DNA but express different genes including variations of gene sequence at the level of RNA (isoforms) in a highly controlled manner that allows complex multicellular organisms to develop. Why RNA isoforms exist and how they are regulated and function is a foundational and unsolved problem in biology with broad implications for predicting and treating diseases. This proposal will continue experimental and computational research towards discovering new aspects of how and why RNA isoforms exist and how they can be used to predict and provide therapeutic targets for treating disease.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Unknown (R35)
Project #
1R35GM139517-01
Application #
10085978
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Bender, Michael T
Project Start
2021-01-01
Project End
2025-12-31
Budget Start
2021-01-01
Budget End
2021-12-31
Support Year
1
Fiscal Year
2021
Total Cost
Indirect Cost
Name
Stanford University
Department
Biochemistry
Type
Schools of Medicine
DUNS #
009214214
City
Stanford
State
CA
Country
United States
Zip Code
94305