K
Karen Meerovitch
Researcher at McGill University
Publications - 25
Citations - 1825
Karen Meerovitch is an academic researcher from McGill University. The author has contributed to research in topics: Translation (biology) & RNA. The author has an hindex of 13, co-authored 25 publications receiving 1791 citations.
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Journal ArticleDOI
Bidirectional RNA helicase activity of eucaryotic translation initiation factors 4A and 4F.
Florence Rozen,Isaac Edery,Karen Meerovitch,Thomas E. Dever,William C. Merrick,Nahum Sonenberg +5 more
TL;DR: In this paper, a simple assay was developed to determine RNA helicase activity, and it was shown that either eIF-4A or eIF 4B, in combination with eIF4B, exhibits helicase activation.
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La autoantigen enhances and corrects aberrant translation of poliovirus RNA in reticulocyte lysate.
Karen Meerovitch,Yuri V. Svitkin,Han S. Lee,F. Lejbkowicz,D. J. Kenan,Edward K. L. Chan,Vadim I. Agol,Jack D. Keene,Nahum Sonenberg +8 more
TL;DR: The results suggest that La protein is involved in poliovirus internal initiation of translation and might function through a similar mechanism in the translation of cellular mRNAs.
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Internal translation initiation on poliovirus RNA: further characterization of La function in poliovirus translation in vitro.
Yuri V. Svitkin,Karen Meerovitch,Han S. Lee,Jaydev N. Dholakia,Daniel J. Kenan,Vadim I. Agol,Nahum Sonenberg +6 more
TL;DR: In this article, the ability of La protein as well as purified initiation factors, eIF-2, guanine nucleotide exchange factor (GEF), eIF4A, EIF-4B and eIF3, to stimulate the synthesis of P1, the capsid precursor protein, in poliovirus type 1 (Mahoney) RNA-programmed RRL was investigated.
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In vitro mutational analysis of cis-acting RNA translational elements within the poliovirus type 2 5' untranslated region.
TL;DR: In vitro translational efficiencies of a series of deletion and point mutations within the 5' UTR of poliovirus type 2 (Lansing strain) RNA are determined and it is demonstrated that the 3' border of the core poliov virus ribosome landing pad is located between nucleotides 556 and 585, whereas a region extending between nucleOTides 585 and 612 confers enhanced translation.
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Hepatitis C virus NS2/3 processing is required for NS3 stability and viral RNA replication.
Sarah Welbourn,Robin Green,Isabelle Gamache,Serge Dandache,Volker Lohmann,Ralf Bartenschlager,Karen Meerovitch,Arnim Pause +7 more
TL;DR: It is proposed that NS2/3 processing is a critical step in the viral life cycle and is required to permit the accumulation of sufficient NS3 for RNA replication to occur and it is demonstrated that uncleaved NS 2/3 degradation can be prevented by the addition of a proteasome inhibitor.