# Regulatory Mechanisms of CD4+ T Cell Differentiation

> **NIH NIH UM1** · DUKE UNIVERSITY · 2020 · $985,050

## Abstract

There is a fundamental gap in understanding how the millions of known regulatory elements
functionally contribute to gene regulation and phenotypes. Continued existence of that gap is an
important problem because, until it is filled, it will remain extremely difficult to identify the genetic
mechanisms underlying the thousands of observed genetic associations with disease phenotypes. Our
long-term goal is to understand how and to what extent gene regulatory elements alter target gene
expression and impact phenotypes. The objectives of this particular proposal are to functionally
characterize all regulatory elements contributing to the differentiation of CD4+ T cells. In doing so, we
will identify the causal regulatory mechanisms that modulate the immune system. The rationale for this
work is that understanding those mechanisms will be the foundation for future efforts to therapeutically
modulate the immune system, and will establish a discovery platform for determining the mechanisms
underlying countless other model systems. Specifically, we will characterize three complementary
components of regulatory element activity: (i) the capacity of regulatory elements to drive expression of
a reporter gene, (ii) the effect of each regulatory element on the expression of one or more target
genes, and (iii) the contributions of regulatory elements to phenotypic function, namely differentiation.
We will accomplish those goals across three specific aims. In Aim 1, we will quantify the activity of all
regulatory elements that have evidence of differential activity between subtypes of mouse CD4 T cells.
We will do so using a capture-based high-throughput reporter assay that allows us to assay larger
(>500 bp) fragments from specific genomic regions of interest. In Aim 2, we will quantify the effects of
regulatory elements on target genes using a novel strategy that combines high-throughput CRISPR/
Cas9-based epigenome editing screens and targeted high-throughput single-cell RNA-sequencing. In
Aim 3, we will determine which regulatory elements are necessary or sufficient for CD4 T cell
differentiation using high-throughput CRISPR/Cas9-based epigenome-editing screens combined
differentiation into particular CD4 T cell subtypes. Each aim will provide functional characterization of all
of the regulatory elements implicated in CD4 T cell differentiation. Together, the aims will provide a
comprehensive, multi-layered, and systematic understanding of the ways that gene regulatory elements
modulate the immune system. The result will be an actionable set of targets for designing strategies to
modulate immune system activity for therapeutic benefit. Because the approach is general to any
model system, the same strategy can be readily transferred to diverse systems including differentiation
and disease models. Therefore, we expect that this project will have both immediate and long-term
benefit for determining the ways that regulatory elements contribute to health and di...

## Key facts

- **NIH application ID:** 9968308
- **Project number:** 5UM1HG009428-04
- **Recipient organization:** DUKE UNIVERSITY
- **Principal Investigator:** GREGORY E CRAWFORD
- **Activity code:** UM1 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2020
- **Award amount:** $985,050
- **Award type:** 5
- **Project period:** 2017-08-21 → 2022-12-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/9968308

## Citation

> US National Institutes of Health, RePORTER application 9968308, Regulatory Mechanisms of CD4+ T Cell Differentiation (5UM1HG009428-04). Retrieved via AI Analytics 2026-05-28 from https://api.ai-analytics.org/grant/nih/9968308. Licensed CC0.

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