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Translation elongation factor 1A is a component of the tombusvirus replicase complex and affects the stability of the p33 replication co-factor

Abstract Host RNA-binding proteins are likely to play multiple, integral roles during replication of plus-strand RNA viruses. To identify host proteins that bind to viral RNAs, we took a global approach based on the yeast proteome microarray, which contains 4080 purified yeast proteins. The biotin-l...

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Published in:Virology (New York, N.Y.) N.Y.), 2009-03, Vol.385 (1), p.245-260
Main Authors: Li, Zhenghe, Pogany, Judit, Panavas, Tadas, Xu, Kai, Esposito, Anthony M, Kinzy, Terri Goss, Nagy, Peter D
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cited_by cdi_FETCH-LOGICAL-c609t-c7d861b92d339e95b95851735f06d8015a51f106eaa7615a4edfb18a23b751333
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container_title Virology (New York, N.Y.)
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creator Li, Zhenghe
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description Abstract Host RNA-binding proteins are likely to play multiple, integral roles during replication of plus-strand RNA viruses. To identify host proteins that bind to viral RNAs, we took a global approach based on the yeast proteome microarray, which contains 4080 purified yeast proteins. The biotin-labeled RNA probes included two distantly related RNA viruses, namely Tomato bushy stunt virus (TBSV) and Brome mosaic virus (BMV). Altogether, we have identified 57 yeast proteins that bound to TBSV RNA and/or BMV RNA. Among the identified host proteins, eleven bound to TBSV RNA and seven bound to BMV RNA with high selectivity, whereas the remaining 39 host proteins bound to both viral RNAs. The interaction between the TBSV replicon RNA and five of the identified host proteins was confirmed via gel-mobility shift and co-purification experiments from yeast. Over-expression of the host proteins in yeast, a model host for TBSV, revealed 4 host proteins that enhanced TBSV replication as well as 14 proteins that inhibited replication. Detailed analysis of one of the identified yeast proteins binding to TBSV RNA, namely translation elongation factor eEF1A, revealed that it is present in the highly purified tombusvirus replicase complex. We also demonstrate binding of eEF1A to the p33 replication protein and a known cis-acting element at the 3′ end of TBSV RNA. Using a functional mutant of eEF1A, we provide evidence on the involvement of eEF1A in TBSV replication.
doi_str_mv 10.1016/j.virol.2008.11.041
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Detailed analysis of one of the identified yeast proteins binding to TBSV RNA, namely translation elongation factor eEF1A, revealed that it is present in the highly purified tombusvirus replicase complex. We also demonstrate binding of eEF1A to the p33 replication protein and a known cis-acting element at the 3′ end of TBSV RNA. Using a functional mutant of eEF1A, we provide evidence on the involvement of eEF1A in TBSV replication.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>19131084</pmid><doi>10.1016/j.virol.2008.11.041</doi><tpages>16</tpages><oa>free_for_read</oa></addata></record>
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ispartof Virology (New York, N.Y.), 2009-03, Vol.385 (1), p.245-260
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source ScienceDirect Journals
subjects 3' Untranslated Regions
Brome mosaic virus
Bromovirus - genetics
Bromovirus - physiology
eEF1A
Gene Expression
Host factor
Infectious Disease
Mutation
Peptide Elongation Factor 1 - genetics
Peptide Elongation Factor 1 - metabolism
Protein array
Proteome array
Replicase
Replication
RNA Replicase - genetics
RNA Replicase - metabolism
RNA, Viral - genetics
RNA, Viral - metabolism
Silencer Elements, Transcriptional
TEF1
Tomato bushy stunt virus
Tombusvirus
Tombusvirus - genetics
Tombusvirus - physiology
Ubiquitin-Protein Ligase Complexes - metabolism
Ubiquitination
Viral Proteins - metabolism
Virus Replication - physiology
Yeast as a model host
Yeasts - metabolism
Yeasts - virology
title Translation elongation factor 1A is a component of the tombusvirus replicase complex and affects the stability of the p33 replication co-factor
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