{"id":67145,"date":"2024-11-23T08:51:39","date_gmt":"2024-11-22T21:51:39","guid":{"rendered":"https:\/\/hudson.org.au?post_type=hdsn_news_post&p=67145"},"modified":"2024-11-23T08:51:47","modified_gmt":"2024-11-22T21:51:47","slug":"uncovering-the-cellular-secrets-of-rna-editing","status":"publish","type":"hdsn_news_post","link":"https:\/\/hudson.org.au\/news\/uncovering-the-cellular-secrets-of-rna-editing\/","title":{"rendered":"Uncovering the cellular secrets of RNA editing"},"content":{"rendered":"\n

Our cells need to be able to recognise potential invaders as a threat, the key function of the body\u2019s innate immune system. Sometimes this process fails causing the body to react to its own cells leading to autoinflammatory disease.  New research has identified a critical fall-back mechanism used by the cells when the usual RNA editing process is switched off.<\/p>\n\n\n\n

Professor Carl Walkley<\/a> heads the RNA Biology and Innate Immune Sensing Research Group at Hudson Institute of Medical Research and their latest research, published in Science Immunology<\/a><\/em>, sheds new light on these crucial processes.<\/p>\n\n\n\n

He explained that cells must be able to determine between their own RNA (“self”) and foreign RNA (“non-self”) that may be a threat, such as a virus.<\/p>\n\n\n\n

\u201cWe know cells use the protein ADAR1 and a process called A-to-I RNA editing as an important way to mark “self” from “non-self” RNA. We have now found a new pathway allowing cells to tolerate losing ADAR1 mediated A-to-I editing, preventing immune reactions from being triggered,\u201d he said.<\/p>\n\n\n

\n
\"Fluorescent
Fluorescent tagged GGNBP2 (red) and CNOT11 (green) in cells<\/em>, which are key regulators of the autoinflammatory response to unedited self dsRNA<\/em>

<\/figcaption><\/figure>\n<\/div>\n\n\n

RNA editing identifies invaders<\/h2>\n\n\n\n

Working with collaborators from the Peter MacCallum Cancer Centre, Victorian Comprehensive Cancer Centre, Spain\u2019s Universidade de Santiago de Compostela, and Stanford University, USA, the team expanded the understanding of how cells can adapt to changes in A-to-I editing and also identifies new ways RNA can be handled in the cell,\u201d he said.<\/p>\n\n\n\n

Among the benefits of this new understanding is potential application in Aicardi-Goutieres Syndrome (AGS), a rare inherited disease affecting the immune system and associated with elevated type I interferon, for which there are currently no effective treatments.<\/p>\n\n\n\n

Prof Walkley said that ADAR1 mutations are one of the causes of AGS: \u201cOur work identifies previously unknown pathways that can allow cells to tolerate a loss of ADAR1 activity. These new pathways or proteins may be new targets to explore as potential treatments of this disease.\u201d<\/p>\n\n\n\n

The multinational research also developed a new cell line model to study loss of ADAR1 functions, as well as isolating key regulators of the autoinflammatory response to unedited self dsRNA and identifying a new pathway regulating the cellular response to immunogenic self dsRNA.<\/p>\n\n\n\n

Innate immunity explained<\/h2>\n\n\n\n

The innate immune system is your body\u2019s first line of defence against harmful invaders like bacteria and viruses. It responds quickly and doesn\u2019t need prior exposure to recognise threats.<\/p>\n\n\n\n

It incorporates physical barriers, such as skin and mucous, cells like macrophages and neutrophils that “eat” germs, and chemical signals like cytokines that trigger inflammation. It also includes specialised proteins in the cell cytoplasm that sense and act to destroy invaders.<\/p>\n\n\n\n

The innate immune system acts as a rapid response team, buying time for the adaptive immune system to kick in if needed.<\/p>\n\n\n\n

A-to-I RNA editing is a process that directly charges the sequence and structure of RNA. It occurs on the cell\u2019s own RNA and we now appreciate that this is an important way that cells can recognise potential RNA threats.<\/p>\n","protected":false},"excerpt":{"rendered":"

Professor Carl Walkley heads the RNA Biology and Innate Immune Sensing Research Group at Hudson Institute of Medical Research and their latest research, published in Science Immunology, sheds new light on these crucial processes.…  Read more<\/a><\/p>\n","protected":false},"featured_media":67142,"menu_order":0,"template":"","issue":[],"tag":[],"story-type":[85],"treatment-type":[92,94],"class_list":["post-67145","hdsn_news_post","type-hdsn_news_post","status-publish","has-post-thumbnail","hentry","story-type-discovery","treatment-type-cell-therapies","treatment-type-immunotherapies"],"acf":[],"yoast_head":"\nUncovering the cellular secrets of RNA editing<\/title>\n<meta name=\"description\" content=\"New research has identified a cellular fall-back mechanism when the usual RNA editing process is switched off.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" 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