# Global analysis of uORF evolution and function

> **NIH NIH R01** · CARNEGIE-MELLON UNIVERSITY · 2020 · $325,891

## Abstract

While variation in gene expression clearly affects the phenotypes of organisms, there is a fundamental
gap in understanding the role of post-transcriptional processes. Because post-transcriptional processes
are critical for the regulation of protein production, addressing this knowledge gap will facilitate better
models of the relationship between genotype and phenotype. upstream Open Reading Frames
(uORFs) are regulatory elements found in most human genes, and some disease-linked mutations
appear to alter the presence of uORFs. Recently, hundreds of uORFs initiating with non-AUG start
codons have been identified in many organisms. Despite the vast number of these elements, the
functions and evolution of AUG and non-AUG uORFs remain elusive. The long-term goal of this project
is to determine the functions and impact of genetic variation in post-transcriptional cis-regulatory
elements. The objective of this proposal is to determine how new uORFs evolve and regulate
translation. Our central hypothesis is that AUG and non-AUG uORFs have different regulatory roles,
leading to different evolutionary trajectories. This hypothesis is based on our preliminary data, as we
have identified hundreds of AUG and non-AUG uORFs with different genomic properties in
Saccharomyces yeasts. We will test our central hypothesis by pursuing the following specific aims: 1)
Investigate the evolution of AUG and non-AUG uORFs; 2) Determine the functions of AUG and non-
AUG uORFs; and 3) Identify the roles of RNA binding proteins in uORF-mediated regulation. In the first
aim, we will identify active uORFs in diverse strains and species of yeasts grown under four conditions
to test the hypothesis that AUG and non-AUG uORFs have different evolutionary tempo and mode. The
second aim will determine the gene-regulatory functions of hundreds of uORFs using FACS-uORF, a
novel dual-fluorescence reporter system we developed. We will use these data to generate predictive
models of uORF function. Aim 3 will identify genome-wide roles of RNA Binding Proteins in regulating
uORFs, and integrate this knowledge in our predictive models. This approach is innovative, in that it
combines exquisite systems biology tools with an excellent model genus to investigate the evolution of
post-transcriptional gene regulation. The proposed research is significant because it is expected to
fundamentally advance the fields of genomics, evolutionary, and systems biology by deciphering the
evolutionary and functional properties of uORFs. Because translation mechanisms are highly
conserved, the knowledge generated by the proposed work is expected to improve models of the
relationship between non-coding genetic variation and phenotype in other eukaryotes, including
humans.

## Key facts

- **NIH application ID:** 9848572
- **Project number:** 5R01GM121895-04
- **Recipient organization:** CARNEGIE-MELLON UNIVERSITY
- **Principal Investigator:** Charles Joel McManus
- **Activity code:** R01 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2020
- **Award amount:** $325,891
- **Award type:** 5
- **Project period:** 2017-02-01 → 2022-01-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/9848572

## Citation

> US National Institutes of Health, RePORTER application 9848572, Global analysis of uORF evolution and function (5R01GM121895-04). Retrieved via AI Analytics 2026-05-24 from https://api.ai-analytics.org/grant/nih/9848572. Licensed CC0.

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