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Homologous SV40 RNA trans-splicing: Special case or prime example of viral RNA trans-splicing?
To date the Simian Virus 40 (SV40) is the only proven example of a virus that recruits the mechanism of RNA trans-splicing to diversify its sequences and gene products. Thereby, two identical viral transcripts are efficiently joined by homologous trans-splicing triggering the formation of a highly t...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Research Network of Computational and Structural Biotechnology
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4151871/ https://www.ncbi.nlm.nih.gov/pubmed/25210599 http://dx.doi.org/10.1016/j.csbj.2014.07.001 |
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author | Poddar, Sushmita Eul, Joachim Patzel, Volker |
author_facet | Poddar, Sushmita Eul, Joachim Patzel, Volker |
author_sort | Poddar, Sushmita |
collection | PubMed |
description | To date the Simian Virus 40 (SV40) is the only proven example of a virus that recruits the mechanism of RNA trans-splicing to diversify its sequences and gene products. Thereby, two identical viral transcripts are efficiently joined by homologous trans-splicing triggering the formation of a highly transforming 100 kDa super T antigen. Sequences of other viruses including HIV-1 and the human adenovirus type 5 were reported to be involved in heterologous trans-splicing towards cellular or viral sequences but the meaning of these events remains unclear. We computationally and experimentally investigated molecular features associated with viral RNA trans-splicing and identified a common pattern: Viral RNA trans-splicing occurs between strong cryptic or regular viral splice sites and strong regular or cryptic splice sites of the trans-splice partner sequences. The majority of these splice sites are supported by exonic splice enhancers. Splice sites that could compete with the trans-splicing sites for cis-splice reactions are weaker or inexistent. Finally, all but one of the trans-splice reactions seem to be facilitated by one or more complementary binding domains of 11 to 16 nucleotides in length which, however occur with a statistical probability close to one for the given length of the involved sequences. The chimeric RNAs generated via heterologous viral RNA trans-splicing either did not lead to fusion proteins or led to proteins of unknown function. Our data suggest that distinct viral RNAs are highly susceptible to trans-splicing and that heterologous viral trans-splicing, unlike homologous SV40 trans-splicing, represents a chance event. |
format | Online Article Text |
id | pubmed-4151871 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Research Network of Computational and Structural Biotechnology |
record_format | MEDLINE/PubMed |
spelling | pubmed-41518712014-09-10 Homologous SV40 RNA trans-splicing: Special case or prime example of viral RNA trans-splicing? Poddar, Sushmita Eul, Joachim Patzel, Volker Comput Struct Biotechnol J Communications To date the Simian Virus 40 (SV40) is the only proven example of a virus that recruits the mechanism of RNA trans-splicing to diversify its sequences and gene products. Thereby, two identical viral transcripts are efficiently joined by homologous trans-splicing triggering the formation of a highly transforming 100 kDa super T antigen. Sequences of other viruses including HIV-1 and the human adenovirus type 5 were reported to be involved in heterologous trans-splicing towards cellular or viral sequences but the meaning of these events remains unclear. We computationally and experimentally investigated molecular features associated with viral RNA trans-splicing and identified a common pattern: Viral RNA trans-splicing occurs between strong cryptic or regular viral splice sites and strong regular or cryptic splice sites of the trans-splice partner sequences. The majority of these splice sites are supported by exonic splice enhancers. Splice sites that could compete with the trans-splicing sites for cis-splice reactions are weaker or inexistent. Finally, all but one of the trans-splice reactions seem to be facilitated by one or more complementary binding domains of 11 to 16 nucleotides in length which, however occur with a statistical probability close to one for the given length of the involved sequences. The chimeric RNAs generated via heterologous viral RNA trans-splicing either did not lead to fusion proteins or led to proteins of unknown function. Our data suggest that distinct viral RNAs are highly susceptible to trans-splicing and that heterologous viral trans-splicing, unlike homologous SV40 trans-splicing, represents a chance event. Research Network of Computational and Structural Biotechnology 2014-07-08 /pmc/articles/PMC4151871/ /pubmed/25210599 http://dx.doi.org/10.1016/j.csbj.2014.07.001 Text en © 2014 Poddar et al. |
spellingShingle | Communications Poddar, Sushmita Eul, Joachim Patzel, Volker Homologous SV40 RNA trans-splicing: Special case or prime example of viral RNA trans-splicing? |
title | Homologous SV40 RNA trans-splicing: Special case or prime example of viral RNA trans-splicing? |
title_full | Homologous SV40 RNA trans-splicing: Special case or prime example of viral RNA trans-splicing? |
title_fullStr | Homologous SV40 RNA trans-splicing: Special case or prime example of viral RNA trans-splicing? |
title_full_unstemmed | Homologous SV40 RNA trans-splicing: Special case or prime example of viral RNA trans-splicing? |
title_short | Homologous SV40 RNA trans-splicing: Special case or prime example of viral RNA trans-splicing? |
title_sort | homologous sv40 rna trans-splicing: special case or prime example of viral rna trans-splicing? |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4151871/ https://www.ncbi.nlm.nih.gov/pubmed/25210599 http://dx.doi.org/10.1016/j.csbj.2014.07.001 |
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