دورية أكاديمية

Dual mechanisms of translation initiation of the full-length HIV-1 mRNA contribute to gag synthesis.

التفاصيل البيبلوغرافية
العنوان: Dual mechanisms of translation initiation of the full-length HIV-1 mRNA contribute to gag synthesis.
المؤلفون: Anne Monette, Fernando Valiente-Echeverría, Matias Rivero, Éric A Cohen, Marcelo Lopez-Lastra, Andrew J Mouland
المصدر: PLoS ONE, Vol 8, Iss 7, p e68108 (2013)
بيانات النشر: Public Library of Science (PLoS), 2013.
سنة النشر: 2013
المجموعة: LCC:Medicine
LCC:Science
مصطلحات موضوعية: Medicine, Science
الوصف: The precursor group-specific antigen (pr55(Gag)) is central to HIV-1 assembly. Its expression alone is sufficient to assemble into virus-like particles. It also selects the genomic RNA for encapsidation and is involved in several important virus-host interactions for viral assembly and restriction, making its synthesis essential for aspects of viral replication. Here, we show that the initiation of translation of the HIV-1 genomic RNA is mediated through both a cap-dependent and an internal ribosome entry site (IRES)-mediated mechanisms. In support of this notion, pr55(Gag) synthesis was maintained at 70% when cap-dependent translation initiation was blocked by the expression of eIF4G- and PABP targeting viral proteases in two in vitro systems and in HIV-1-expressing cells directly infected with poliovirus. While our data reveal that IRES-dependent translation of the viral genomic RNA ensures pr55(Gag) expression, the synthesis of other HIV-1 proteins, including that of pr160(Gag/Pol), Vpr and Tat is suppressed early during progressive poliovirus infection. The data presented herein implies that the unspliced HIV-1 genomic RNA utilizes both cap-dependent and IRES-dependent translation initiation to supply pr55(Gag) for virus assembly and production.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1932-6203
Relation: http://europepmc.org/articles/PMC3702555?pdf=render; https://doaj.org/toc/1932-6203
DOI: 10.1371/journal.pone.0068108
URL الوصول: https://doaj.org/article/40f6f1df2e9c4dc7bc7bc1f6d2a291fb
رقم الأكسشن: edsdoj.40f6f1df2e9c4dc7bc7bc1f6d2a291fb
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:19326203
DOI:10.1371/journal.pone.0068108