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- Publisher Website: 10.1073/pnas.93.7.3138
- Scopus: eid_2-s2.0-0029920996
- PMID: 8610182
- WOS: WOS:A1996UD37500096
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Article: The open reading frame of bamboo mosaic potexvirus satellite RNA is not essential for its replication and can be replaced with a bacterial gene
Title | The open reading frame of bamboo mosaic potexvirus satellite RNA is not essential for its replication and can be replaced with a bacterial gene |
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Authors | |
Keywords | Chemicals And Cas Registry Numbers |
Issue Date | 1996 |
Publisher | National Academy of Sciences. The Journal's web site is located at http://www.pnas.org |
Citation | Proceedings of the National Academy of Sciences of the United States of America, 1996, v. 93 n. 7, p. 3138-3142 How to Cite? |
Abstract | A satellite RNA of 836 nt depends on the bamboo mosaic potexvirus (BaMV) for its replication and encapsidation. The BaMV satellite RNA (satBaMV) contains a single open reading frame encoding a 20-kDa nonstructural protein. A full-length infectious cDNA clone has been generated downstream of the T7 RNA polymerase promoter. To investigate the role of the 20-kDa protein encoded by satBaMV, satBaMV transcripts containing mutations in the open reading frame were tented for their ability to replicate in barley protoplasts and in Chenopodium quinoa using BaMV RNA as a helper genome. Unlike other large satellite RNAs, mutants in the open reading frame did not block their replication, suggesting that the 20-kDa protein is not essential for satBaMV replication. Precise replacement of the open reading frame with sequences encoding chloramphenicol acetyltransferase resulted in high level expression of chloramphenicol acetyltransferase in infected C. quinoa, indicating that satBaMV is potentially useful as a satellite-based expression vector. |
Persistent Identifier | http://hdl.handle.net/10722/91036 |
ISSN | 2023 Impact Factor: 9.4 2023 SCImago Journal Rankings: 3.737 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
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dc.contributor.author | Lin, N-S | en_HK |
dc.contributor.author | Lee, Y-S | en_HK |
dc.contributor.author | Lin, B-Y | en_HK |
dc.contributor.author | Lee, C-W | en_HK |
dc.contributor.author | Hsu, Y-H | en_HK |
dc.date.accessioned | 2010-09-17T10:12:05Z | - |
dc.date.available | 2010-09-17T10:12:05Z | - |
dc.date.issued | 1996 | en_HK |
dc.identifier.citation | Proceedings of the National Academy of Sciences of the United States of America, 1996, v. 93 n. 7, p. 3138-3142 | en_HK |
dc.identifier.issn | 0027-8424 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/91036 | - |
dc.description.abstract | A satellite RNA of 836 nt depends on the bamboo mosaic potexvirus (BaMV) for its replication and encapsidation. The BaMV satellite RNA (satBaMV) contains a single open reading frame encoding a 20-kDa nonstructural protein. A full-length infectious cDNA clone has been generated downstream of the T7 RNA polymerase promoter. To investigate the role of the 20-kDa protein encoded by satBaMV, satBaMV transcripts containing mutations in the open reading frame were tented for their ability to replicate in barley protoplasts and in Chenopodium quinoa using BaMV RNA as a helper genome. Unlike other large satellite RNAs, mutants in the open reading frame did not block their replication, suggesting that the 20-kDa protein is not essential for satBaMV replication. Precise replacement of the open reading frame with sequences encoding chloramphenicol acetyltransferase resulted in high level expression of chloramphenicol acetyltransferase in infected C. quinoa, indicating that satBaMV is potentially useful as a satellite-based expression vector. | en_HK |
dc.language | eng | en_HK |
dc.publisher | National Academy of Sciences. The Journal's web site is located at http://www.pnas.org | en_HK |
dc.relation.ispartof | Proceedings of the National Academy of Sciences of the United States of America | en_HK |
dc.subject | Chemicals And Cas Registry Numbers | en_HK |
dc.title | The open reading frame of bamboo mosaic potexvirus satellite RNA is not essential for its replication and can be replaced with a bacterial gene | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Lin, B:blin@hku.hk | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1073/pnas.93.7.3138 | en_HK |
dc.identifier.pmid | 8610182 | - |
dc.identifier.scopus | eid_2-s2.0-0029920996 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-0029920996&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 93 | en_HK |
dc.identifier.issue | 7 | en_HK |
dc.identifier.spage | 3138 | en_HK |
dc.identifier.epage | 3142 | en_HK |
dc.identifier.isi | WOS:A1996UD37500096 | - |
dc.identifier.issnl | 0027-8424 | - |