# Capturing the dynamic epigenome using single molecule and single cell approaches

> **NIH NIH R35** · UNIVERSITY OF MICHIGAN AT ANN ARBOR · 2021 · $9,513

## Abstract

Abstract:
Our bodies consist of billions of genetically identical cells that can exhibit distinct phenotypic or epigenetic
states. The covalent and reversible modification of histones enables cells to establish heritable gene
expression patterns without altering their genetic blueprint. Epigenetic mechanisms that control gene
expression are essential to maintain cellular identity and program multicellular differentiation. Histone H3 lysine
9 methylation (H3K9me) is associated with transcription silencing and heterochromatin formation. Fission yeast
(S. pombe) has a minimalist heterochromatin architecture that is amenable to high-throughput genetics and
biochemistry. A trio of conserved proteins regulates heterochromatin, which includes, 1) an H3K9me specific
''writer,'' Clr4Suv39h that catalyzes H3K9me 2) an H3K9me specific ''reader,'' Swi6HP1 that binds to H3K9me
chromatin and silences transcription and, 3) an H3K9me specific ''eraser,'' Epe1JmjC, that opposes
heterochromatin assembly and epigenetic inheritance. Fusing Clr4 to the tetracycline-inducible TetR DNA
binding domain facilitates rapid and reversible control of heterochromatin assembly. My lab’s innovative
genetic strategy has enabled us to identify chromatin-associated factors with unique roles that are restricted to
heterochromatin maintenance. During the summer research experience supported by the supplement award,
the undergraduate student will focus on generating new protein variants using a PCR based mutagenesis
approach to identify alleles that enhance or suppress epigenetic inheritance. The research experience is
designed to promote the technical, operation and professional skills of the candidate. The research experience
is also aligned with the candidate’s future career aspirations to be a part of the biomedical workforce and
pursue a graduate education. Furthermore,all of the scientific goals described here are fully consistent with the
proposed research directions of the parent award.

## Key facts

- **NIH application ID:** 10392269
- **Project number:** 3R35GM137832-01S1
- **Recipient organization:** UNIVERSITY OF MICHIGAN AT ANN ARBOR
- **Principal Investigator:** Kaushik Ragunathan
- **Activity code:** R35 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2021
- **Award amount:** $9,513
- **Award type:** 3
- **Project period:** 2020-08-01 → 2025-07-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10392269

## Citation

> US National Institutes of Health, RePORTER application 10392269, Capturing the dynamic epigenome using single molecule and single cell approaches (3R35GM137832-01S1). Retrieved via AI Analytics 2026-05-25 from https://api.ai-analytics.org/grant/nih/10392269. Licensed CC0.

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