Active Genetics & Molecular Biology Cells, Biochemistry & Physiology

Discovering how CpG islands control transcription to regulate gene expression

In plain English

AI plain-English summary

Every cell in the human body carries the same DNA, yet a skin cell and a nerve cell behave completely differently—because each one switches on a different set of genes. This project aims to crack the code of how those switches work. The problem is that we do not fully understand how CpG islands—short stretches of DNA near many genes—help decide whether a gene is turned on or off. Researchers know these islands guide the formation of specialised chromatin states (the packaging of DNA inside cells), but the precise mechanism by which those states control gene activity remains a central mystery in fundamental biology. This is curiosity-driven fundamental science. If successful, it will produce a quantitative, predictive model of how gene promoters function—a framework that could eventually help explain what goes wrong when gene regulation breaks down in diseases such as cancer or developmental disorders. Past discoveries in gene regulation have led to technologies like mRNA vaccines and targeted cancer therapies; this work lays similar groundwork for future applications that are not yet foreseeable.

View original technical description
The remarkable process of multicellular development requires that cells initiate and then maintain highly-defined gene expression programs. We have recently discovered that CpG island (CGI) elements guide the formation of distinct chromatin-states at gene promoters and these play a fundamental role in specifying appropriate gene expression. Despite these advances, how CGI- guided chromatin-states control transcription to regulate gene expression remains enigmatic and is a central outstanding question in our most basic understanding of gene regulation. Here we will use a bold, multidisciplinary, and collaborative approach to discover how CGI-defined chromatin-states control transcription to repress (Aim1) or enable (Aim2) gene expression, and use this new mechanistic insight to test our hypothesis that CGIs integrate chromatin-based activities to create decisive switch-like transitions in gene expression during cell lineage commitment (Aim3). In addressing these important questions, our new discoveries will enable us to develop a quantitative and predictive model for CGI-dependent gene regulation and in doing so redefine our understanding of how gene promoters function to control gene expression in normal and disease biology.

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Researchers

Martin Howard (EPMC Awardee)Robert Klose (EPMC Awardee)

Related Research

Grants with similar aims, by meaning.

Understanding the role of CpG islands in gene regulatory element function and transcription.
Understanding how Trithorax & Polycomb group proteins control gene expression from CpG islands
Determining how distinct vertebrate promoter classes coordinate cis-regulatory input.
Transcriptional control of cell fate decisions by chromatin remodelling proteins
Biochemical isolation and mass spectrometric analysis of the CpG island proteome

Original classification

Discovery Award

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