Effects of messenger RNA structure and other translational control mechanisms on major histocompatibility complex‐I mediated antigen presentation. (26th September 2014)
- Record Type:
- Journal Article
- Title:
- Effects of messenger RNA structure and other translational control mechanisms on major histocompatibility complex‐I mediated antigen presentation. (26th September 2014)
- Main Title:
- Effects of messenger RNA structure and other translational control mechanisms on major histocompatibility complex‐I mediated antigen presentation
- Authors:
- Murat, Pierre
Tellam, Judy - Abstract:
- <abstract abstract-type="main" id="wrna1262-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <p id="wrna1262-para-0001">Effective T‐cell surveillance of antigen‐presenting cells is dependent on the expression of an array of antigenic peptides bound to major histocompatibility complex (MHC) class I (MHC‐I) or class II (MHC‐II) molecules<italic>.</italic> Pathogens co‐evolving with their hosts exploit crucial translational regulatory mechanisms in order to evade host immune recognition and thereby sustain their infection. Evasion strategies that downregulate viral protein synthesis and thereby restrict antigen presentation to cytotoxic T‐cells through the endogenous MHC‐I pathway have been implicated in the pathogenesis of viral‐associated malignancies. An understanding of the mechanisms by which messenger RNA (mRNA) structure modulates both viral mRNA translation and the antigen processing machinery to escape immune surveillance, will stimulate the development of alternative therapeutic strategies focused on RNA‐directed drugs designed to enhance immune responses against infected cells. In this review, we discuss regulatory aspects of the MHC‐I pathway and summarize current knowledge of the role attributed by mRNA structure and other translational regulatory mechanisms in immune evasion. In particular we highlight the impact of recently identified G‐quadruplex structures within virally encoded transcripts as unique regulatory signals for translational control<abstract abstract-type="main" id="wrna1262-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <p id="wrna1262-para-0001">Effective T‐cell surveillance of antigen‐presenting cells is dependent on the expression of an array of antigenic peptides bound to major histocompatibility complex (MHC) class I (MHC‐I) or class II (MHC‐II) molecules<italic>.</italic> Pathogens co‐evolving with their hosts exploit crucial translational regulatory mechanisms in order to evade host immune recognition and thereby sustain their infection. Evasion strategies that downregulate viral protein synthesis and thereby restrict antigen presentation to cytotoxic T‐cells through the endogenous MHC‐I pathway have been implicated in the pathogenesis of viral‐associated malignancies. An understanding of the mechanisms by which messenger RNA (mRNA) structure modulates both viral mRNA translation and the antigen processing machinery to escape immune surveillance, will stimulate the development of alternative therapeutic strategies focused on RNA‐directed drugs designed to enhance immune responses against infected cells. In this review, we discuss regulatory aspects of the MHC‐I pathway and summarize current knowledge of the role attributed by mRNA structure and other translational regulatory mechanisms in immune evasion. In particular we highlight the impact of recently identified G‐quadruplex structures within virally encoded transcripts as unique regulatory signals for translational control and antigen presentation. <italic>WIREs RNA</italic> 2015, 6:157–171. doi: 10.1002/wrna.1262</p> <p id="wrna1262-para-0002">Conflict of interest: The authors have declared no conflicts of interest for this article.</p> <p>For further resources related to this article, please visit the <ext-link ext-link-type="uri" xlink:href="http://wires.wiley.com/remdoi.cgi?doi=10.1002/wrna.1262" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink">WIREs website</ext-link>.</p> </abstract> … (more)
- Is Part Of:
- Wiley interdisciplinary reviews. Volume 6:Number 2(2015:Mar./Apr.)
- Journal:
- Wiley interdisciplinary reviews
- Issue:
- Volume 6:Number 2(2015:Mar./Apr.)
- Issue Display:
- Volume 6, Issue 2 (2015)
- Year:
- 2015
- Volume:
- 6
- Issue:
- 2
- Issue Sort Value:
- 2015-0006-0002-0000
- Page Start:
- 157
- Page End:
- 171
- Publication Date:
- 2014-09-26
- Subjects:
- RNA -- Periodicals
572.8805 - Journal URLs:
- http://helicon.vuw.ac.nz/login?url=http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1757-7012 ↗
http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1757-7012 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/wrna.1262 ↗
- Languages:
- English
- ISSNs:
- 1757-7004
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 9317.862404
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3847.xml