Active Genetics & Molecular Biology Cells, Biochemistry & Physiology

Decoding riboregulation in complex cellular behaviour of bacteria

In plain English

AI plain-English summary

Bacteria rely on RNA molecules to decide whether to become infectious or resistant to antibiotics, and this project will map the molecular machines that control those decisions. RNA is best known for carrying genetic instructions from DNA to the protein-making machinery, but it does far more. In bacteria, RNA molecules are constantly being made, folded, modified, and destroyed. The protein complexes that manage these processes determine which genes are active and when. This project will isolate those complexes, solve their three-dimensional structures, and watch them work inside living cells. The goal is to understand the rules that govern an RNA molecule's lifetime and its ultimate biological effect. This is fundamental science. It will not produce a drug or a diagnostic tomorrow. But bacterial virulence and antibiotic resistance are controlled by RNA-based regulatory networks. Understanding how those networks operate—how a bacterium decides to switch from harmless to dangerous, or from drug-sensitive to drug-resistant—could eventually reveal new targets for therapies that disrupt those decisions. Past work on bacterial RNA regulation has already yielded tools like CRISPR, which began as a study of how bacteria store memories of viral infections.

View original technical description
In cells from every domain of life, RNA acts to communicate hereditary information, to regulate gene expression, and to support network control. Therefore, the fates of diverse RNA molecules, their biogenesis and lifetime, play a critical role in determining complex cellular behaviour. We propose to investigate the processes that govern RNA fate in bacteria. We hypothesise that defined ribonucleoprotein complexes act in key steps of cellular control, including co-transcriptional ribonucleoprotein folding and surveillance of transcripts during translation. We will test this experimentally and will also seek to understand how such complexes might be linked to sensing and responding to cellular status, including metabolic remodelling. To this end, we will study the structure and function of key RNA-processing complexes in model bacterial species. Our targets include both stable protein-RNA complexes, which will be isolated and examined by high-resolution structural and functional analysis, and more transient assemblies, which will need to be investigated inside the cells to capture their information-rich physiological states. Our work will help to elaborate rules that define the lifetime and biological impact of RNA and its contribution to complex cellular phenotypes, including infectious virulence and antibiotic resistance of various bacterial species.

View the original record at the funder ↗

Researchers

Bonaventura LUISI (EPMC Awardee)

Related Research

Grants with similar aims, by meaning.

The molecular machinery of RNA metabolism and riboregulation in bacteria
Organisation and regulation of bacterial enhancer-binding proteins
Exploring the spatiotemporal functioning and regulation of RNA Polymerases in the live Escherichia coli bacterium
Structure-based functional analysis of RNA Polymerase
Interplay of bacterial transcription and chromosome organisation in vivo

Original classification

Investigator Award in Science

Plain English summaries and category classifications on this site are generated by AI and may not perfectly reflect the original research.