Completed Genetics & Molecular Biology Cells, Biochemistry & Physiology

R-loop coupled chromatin regulation

In plain English

AI plain-English summary

Every cell in your body contains thousands of tiny lasso-like structures called R-loops—hybrids of RNA and DNA that loop back and grab onto the genome—and scientists have only a vague idea of what most of them actually do. R-loops were first noticed for their ability to break DNA, but they now appear to be central to how genes are switched on and off, how chromosomes are packaged, and how cells repair their own genetic material. The problem is that no one knows how these structures are built or taken apart, or how they manage to influence so many different processes at once. This project will focus on a single, well-studied R-loop in a simple organism to trace exactly which proteins assemble it, which dismantle it, and how it coordinates transcription with DNA replication. If successful, this work will provide the first detailed molecular blueprint of how an R-loop controls gene expression and chromosome structure. Because R-loops are found in virtually all organisms—from yeast to humans—the principles uncovered here will apply broadly. This is fundamental science: it will not produce a drug or a diagnostic tomorrow. But understanding how R-loops work could eventually explain why they go wrong in cancers and neurological disorders, where they accumulate at harmful levels.

View original technical description
Non-canonical chromatin structures are emerging as important components of gene regulation. One example, RNA-DNA hybrid structures known as R-loops, occur frequently in many genomes. Initially studied with respect to genome instability, they have now been linked to transcriptional regulation, heterochromatin formation and recombination. But exactly what regulates R-loop dynamics, and how R-loops influence local chromatin states to affect a wide range of chromatin processes is still poorly understood. Deriving mechanistic understanding of R-loops from genome wide analyses is difficult. We will therefore focus on one functionally important R-loop and exploit a genetically tractable system and a wealth of information to develop deep mechanistic understanding into the regulation and role of an R-loop. We will identify novel factors that stabilize and resolve the R-loop, and establish how their functions are integrated. We will investigate whether the R-loop sets up a transcription-replication conflict that propagates heterochromatinization of the locus, thus setting the expression state. We will also dissect if R-loop dynamics and a gene loop influence promoter dominance to co-ordinate sense and antisense transcription. Active collaborations will enable a broad set of approaches to be used and concepts to be compared between organisms.

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Researchers

Caroline Dean (EPMC Awardee)

Related Research

Grants with similar aims, by meaning.

Mechanisms of R-loop formation in mammals: Interplay with RNA polymerase II regulation and epigenetic modifications.
Dynamic regulation of chromatin loops by cohesins and CTCF in real time: physiology and pathology
R-loops: from molecular principles to their roles in human disease
RNA-DNA hybrids as a source of genome instability in cancer
Cryo-EM studies of Gene Loops and Transcription Control

Original classification

Investigator Award in Science

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