# Regulation of cardiac patterning via Akirin/NuRD Interactions

> **NIH NIH R15** · KENNESAW STATE UNIVERSITY · 2022 · $406,267

## Abstract

Project Summary
Congenital heart defects are the most prevalent birth defects in the human population, with an incident rate as
high as 10 in 1000 live births. A significant number of these cases are termed sporadic, which are largely the
result of interactions between a number of independent genetic loci and alleles. To aid in our understanding of
the polygenic nature of congenital heart defects, it remains imperative to continue to identify new gene
regulatory partners that may play a role in the process of embryonic heart patterning. Our laboratory has
recently identified a cofactor, Akirin, that is responsible for interfacing transcription factor activity with chromatin
remodeling machinery to facilitate gene expression. Importantly, Akirin appears to play a role in the proper
patterning and morphogenesis of the embryonic heart in Drosophila melanogaster. Excitingly, our preliminary
data suggests that Akirin likely regulates insect embryonic heart development through interactions with the
CHD4/NuRD family of chromatin remodeling machinery. This mechanism of Akirin/NuRD interactions for
expression of cardiac developmental gene pathways appears to be conserved from mammals to insects.
To further determine the role of Akirin/NuRD interactions in the process of heart development, we propose two
specific aims: 1) Using a combination of genetic, biochemical, and live imaging techniques, will confirm the
importance of Akirin/NuRD interactions during development, and 2) We will employ both next-generation
massively parallel RNA sequencing methods, as well as ATAC-seq and conventional chromatin
immunoprecipitation methods to determine the gene regulatory role of Akirin during cardiac myogenesis. This
work will provide key data for understanding the role of Akirin in the process of heart formation, and provide a
new avenue for studying and/or preventing causes of congenital heart defects.
Critically, in keeping with the goals of the AREA award mechanism, this project will give undergraduate
researchers hands-on experience in a wide variety of molecular, genetic, histological, microscopic, and
biochemical techniques, which will provide a valuable skill set for a future career in biomedical research.

## Key facts

- **NIH application ID:** 10514703
- **Project number:** 1R15HL161738-01A1
- **Recipient organization:** KENNESAW STATE UNIVERSITY
- **Principal Investigator:** Anton Bryantsev
- **Activity code:** R15 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2022
- **Award amount:** $406,267
- **Award type:** 1
- **Project period:** 2022-09-05 → 2026-08-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10514703

## Citation

> US National Institutes of Health, RePORTER application 10514703, Regulation of cardiac patterning via Akirin/NuRD Interactions (1R15HL161738-01A1). Retrieved via AI Analytics 2026-05-29 from https://api.ai-analytics.org/grant/nih/10514703. Licensed CC0.

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