CMV MIRNAS · Function and mechanism of viral miRNAs in cytomegalovirus infection
6РП — Действия „Мария Кюри“
- Период
- 2007-03-01 → 2009-02-28
- Финансиране от ЕС
- 160 180 €
- Участници
- 1
- Схема
- IIF
Линиите свързват координатора с партньорите.
Накратко на български
МикроРНК-тата на цитомегаловируса се анализират, за да се разбере как тези малки молекули регулират гените на клетката и самия вирус. Познаването на тези механизми помага при разработването на антивирусни терапии и ваксини срещу инфекции при трансплантирани пациенти и новородени.
Кратко обяснение, генерирано от езиков модел по текста на CORDIS. Оригиналът е по-долу.
Резултати накратко
Final Activity Report Summary - CMV MIRNAS (Function and mechanism of viral miRNAs in cytomegalovirus infection)
This research has focused on a virus, cytomegalovirus (CMV), that harmlessly infects healthy people, but has devastating and often fatal consequences for immune suppressed patients, especially those undergoing transplantation. Human CMV (HCMV) is also the leading cause of congenital infection in humans, resulting in severe central nervous system damage. Accordingly, there is a need to understand the fundamental biology of the virus in order to develop anti-viral therapeutics and ultimately a vaccination. This project was aimed at addressing the role of small ribonucleic acids (microRNAs) in CMV pathogenesis and the mechanism by which a microRNA can influence the outcome of viral infection. Viral-encoded microRNAs were first discovered in Epstein-Barr virus (EBV) in 2004 and have been shown to regulate host cell genes involved in the immune response as well as viral genes important for latency. Reports to date have been limited to in vitro observations; a true understanding of viral microRNA function requires analysis in an intact physiological system. Towards this goal, the first objective here was to identify microRNAs in MCMV, where the natural virus can be examined in its natural host. Operating under the assumption that MCMV would encode these small RNAs (based on bioinformatic predictions and reports with human CMV), we set out to identify these RNAs using cloning and bioinformatic analysis. The small RNAs identified were then validated in multiple cell types and characterized to determine when in the viral life cycle they are expressed (published in the Journal of Virology). This has laid the groundwork for further in vitro and in vivo analysis of MCMV microRNA function and we are currently analysing the targets of a subset of the highly expressed MCMV microRNAs. The MCMV microRNAs also possess some unusual regulatory properties that merit further analysis and may shed light on microRNA regulation relevant to various disease processes.
Текст от CORDIS, на английски · Данни: CORDIS, © Европейски съюз
Цел на проекта
This project addresses a fundamental and pressing question in gene regulation: the function of microRNAs (miRNAs). Discovered only in the last decade, these small (~22 nt) RNAs represent an important new class of molecules and are expected to play large, and previously unrecognized, roles in numerous cellular pathways.We propose to use murine cytomegalovirus (MCMV) as a tool to study miRNA function, by examining the target specificity of the MCMV miRNAs, and the influence of the miRNAs on the gene pathways involved in infection. Specifically, this project will utilize microarray and proteomic strategies to define the gene factors whose expression is altered by viral miRNAs.Results will be mapped onto viral and host gene networks in order to examine the local or global influence of each miRNA. Overall, the planned studies will provide critical new information on the function of mircroRNAs in a viral system and will shed light on viral/host interactions important for infection.The results will provide an important framework with which to evaluate miRNA function in other (potentially more complex) systems. Novel detection strategies for miRNAs will also be explored, as these RNA molecules are expected to represent a new class of biomarkers.
Оригинален текст от CORDIS (на английски).
Участници
- UNIVERSITY OF EDINBURGH · EDINBURGHКоординаторОбединеното кралство
Връзки
Данни: CORDIS, © Европейски съюз
