Stability of a Long Noncoding Viral RNA Depends on a 9-nt Core Element at the RNA 5' End to Interact with Viral ORF57 and Cellular PABPC1

<p>Kaposi sarcoma-associated herpesvirus (KSHV) ORF57, also known as Mta (<u>m</u>RNA <u>t</u>ranscript <u>a</u>ccumulation), enhances viral intron-less transcript accumulation and promotes splicing of intron-containing viral RNA transcripts. In this study,...

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Main Author: Maria J. Massimelli, Jeong-Gu Kang, Vladimir Majerciak, Shu-Yun Le, David J. Liewehr, Seth M. Steinberg, Zhi-Ming Zheng
Format: Article
Language:English
Published: Ivyspring International Publisher 2011-01-01
Series:International Journal of Biological Sciences
Online Access:http://www.biolsci.org/v07p1145.htm
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author Maria J. Massimelli, Jeong-Gu Kang, Vladimir Majerciak, Shu-Yun Le, David J. Liewehr, Seth M. Steinberg, Zhi-Ming Zheng
author_facet Maria J. Massimelli, Jeong-Gu Kang, Vladimir Majerciak, Shu-Yun Le, David J. Liewehr, Seth M. Steinberg, Zhi-Ming Zheng
author_sort Maria J. Massimelli, Jeong-Gu Kang, Vladimir Majerciak, Shu-Yun Le, David J. Liewehr, Seth M. Steinberg, Zhi-Ming Zheng
collection DOAJ
description <p>Kaposi sarcoma-associated herpesvirus (KSHV) ORF57, also known as Mta (<u>m</u>RNA <u>t</u>ranscript <u>a</u>ccumulation), enhances viral intron-less transcript accumulation and promotes splicing of intron-containing viral RNA transcripts. In this study, we identified KSHV PAN, a long non-coding <u>p</u>oly<u>a</u>denylated <u>n</u>uclear RNA as a main target of ORF57 by a genome-wide CLIP (cross-linking and immunoprecipitation) approach. KSHV genome lacking ORF57 expresses only a minimal amount of PAN. In cotransfection experiments, ORF57 alone increased PAN expression by 20-30-fold when compared to vector control. This accumulation function of ORF57 was dependent on a structured RNA element in the 5' PAN, named MRE (<u>M</u>ta <u>r</u>esponsive <u>e</u>lement), but not much so on an ENE (expression and nuclear retention element) in the 3' PAN previously reported by other studies. We showed that the major function of the 5' PAN MRE is increasing the RNA half-life of PAN in the presence of ORF57. Further mutational analyses revealed a core motif consisting of 9 nucleotides in the MRE-II , which is responsible for ORF57 interaction and function. The 9-nt core in the MRE-II also binds cellular PABPC1, but not the E1B-AP5 which binds another region of the MRE-II. In addition, we found that PAN RNA is partially exportable in the presence of ORF57. Together, our data provide compelling evidence as to how ORF57 functions to accumulate a non-coding viral RNA in the course of virus lytic infection.</p>
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spelling doaj.art-6a07f9eabb9a45f484d7c0f094c2f4f02022-12-21T18:21:18ZengIvyspring International PublisherInternational Journal of Biological Sciences1449-22882011-01-017811451160Stability of a Long Noncoding Viral RNA Depends on a 9-nt Core Element at the RNA 5' End to Interact with Viral ORF57 and Cellular PABPC1Maria J. Massimelli, Jeong-Gu Kang, Vladimir Majerciak, Shu-Yun Le, David J. Liewehr, Seth M. Steinberg, Zhi-Ming Zheng<p>Kaposi sarcoma-associated herpesvirus (KSHV) ORF57, also known as Mta (<u>m</u>RNA <u>t</u>ranscript <u>a</u>ccumulation), enhances viral intron-less transcript accumulation and promotes splicing of intron-containing viral RNA transcripts. In this study, we identified KSHV PAN, a long non-coding <u>p</u>oly<u>a</u>denylated <u>n</u>uclear RNA as a main target of ORF57 by a genome-wide CLIP (cross-linking and immunoprecipitation) approach. KSHV genome lacking ORF57 expresses only a minimal amount of PAN. In cotransfection experiments, ORF57 alone increased PAN expression by 20-30-fold when compared to vector control. This accumulation function of ORF57 was dependent on a structured RNA element in the 5' PAN, named MRE (<u>M</u>ta <u>r</u>esponsive <u>e</u>lement), but not much so on an ENE (expression and nuclear retention element) in the 3' PAN previously reported by other studies. We showed that the major function of the 5' PAN MRE is increasing the RNA half-life of PAN in the presence of ORF57. Further mutational analyses revealed a core motif consisting of 9 nucleotides in the MRE-II , which is responsible for ORF57 interaction and function. The 9-nt core in the MRE-II also binds cellular PABPC1, but not the E1B-AP5 which binds another region of the MRE-II. In addition, we found that PAN RNA is partially exportable in the presence of ORF57. Together, our data provide compelling evidence as to how ORF57 functions to accumulate a non-coding viral RNA in the course of virus lytic infection.</p>http://www.biolsci.org/v07p1145.htm
spellingShingle Maria J. Massimelli, Jeong-Gu Kang, Vladimir Majerciak, Shu-Yun Le, David J. Liewehr, Seth M. Steinberg, Zhi-Ming Zheng
Stability of a Long Noncoding Viral RNA Depends on a 9-nt Core Element at the RNA 5' End to Interact with Viral ORF57 and Cellular PABPC1
International Journal of Biological Sciences
title Stability of a Long Noncoding Viral RNA Depends on a 9-nt Core Element at the RNA 5' End to Interact with Viral ORF57 and Cellular PABPC1
title_full Stability of a Long Noncoding Viral RNA Depends on a 9-nt Core Element at the RNA 5' End to Interact with Viral ORF57 and Cellular PABPC1
title_fullStr Stability of a Long Noncoding Viral RNA Depends on a 9-nt Core Element at the RNA 5' End to Interact with Viral ORF57 and Cellular PABPC1
title_full_unstemmed Stability of a Long Noncoding Viral RNA Depends on a 9-nt Core Element at the RNA 5' End to Interact with Viral ORF57 and Cellular PABPC1
title_short Stability of a Long Noncoding Viral RNA Depends on a 9-nt Core Element at the RNA 5' End to Interact with Viral ORF57 and Cellular PABPC1
title_sort stability of a long noncoding viral rna depends on a 9 nt core element at the rna 5 end to interact with viral orf57 and cellular pabpc1
url http://www.biolsci.org/v07p1145.htm
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