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Complete Genome Sequence of a UL96 Mutant Cytomegalovirus Towne-BAC (Bacterial Artificial Chromosome) Isolate Passaged in Fibroblasts To Allow Accumulation of Compensatory Mutations
Here, we present the complete genome sequence of a cytomegalovirus Towne-BAC (bacterial artificial chromosome) isolate that we first genetically engineered to mutate the UL96 gene and then serially passaged in human fibroblasts to allow for the accumulation of compensatory mutations. A total of 17 s...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3813188/ https://www.ncbi.nlm.nih.gov/pubmed/24158558 http://dx.doi.org/10.1128/genomeA.00901-13 |
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author | Brechtel, Teal M. Tyner, Molly Tandon, Ritesh |
author_facet | Brechtel, Teal M. Tyner, Molly Tandon, Ritesh |
author_sort | Brechtel, Teal M. |
collection | PubMed |
description | Here, we present the complete genome sequence of a cytomegalovirus Towne-BAC (bacterial artificial chromosome) isolate that we first genetically engineered to mutate the UL96 gene and then serially passaged in human fibroblasts to allow for the accumulation of compensatory mutations. A total of 17 single-base substitutions were discovered in the passaged genome compared to the reference sequence (KF493877). |
format | Online Article Text |
id | pubmed-3813188 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-38131882013-10-31 Complete Genome Sequence of a UL96 Mutant Cytomegalovirus Towne-BAC (Bacterial Artificial Chromosome) Isolate Passaged in Fibroblasts To Allow Accumulation of Compensatory Mutations Brechtel, Teal M. Tyner, Molly Tandon, Ritesh Genome Announc Viruses Here, we present the complete genome sequence of a cytomegalovirus Towne-BAC (bacterial artificial chromosome) isolate that we first genetically engineered to mutate the UL96 gene and then serially passaged in human fibroblasts to allow for the accumulation of compensatory mutations. A total of 17 single-base substitutions were discovered in the passaged genome compared to the reference sequence (KF493877). American Society for Microbiology 2013-10-24 /pmc/articles/PMC3813188/ /pubmed/24158558 http://dx.doi.org/10.1128/genomeA.00901-13 Text en Copyright © 2013 Brechtel et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 3.0 Unported license (http://creativecommons.org/licenses/by/3.0/) . |
spellingShingle | Viruses Brechtel, Teal M. Tyner, Molly Tandon, Ritesh Complete Genome Sequence of a UL96 Mutant Cytomegalovirus Towne-BAC (Bacterial Artificial Chromosome) Isolate Passaged in Fibroblasts To Allow Accumulation of Compensatory Mutations |
title | Complete Genome Sequence of a UL96 Mutant Cytomegalovirus Towne-BAC (Bacterial Artificial Chromosome) Isolate Passaged in Fibroblasts To Allow Accumulation of Compensatory Mutations |
title_full | Complete Genome Sequence of a UL96 Mutant Cytomegalovirus Towne-BAC (Bacterial Artificial Chromosome) Isolate Passaged in Fibroblasts To Allow Accumulation of Compensatory Mutations |
title_fullStr | Complete Genome Sequence of a UL96 Mutant Cytomegalovirus Towne-BAC (Bacterial Artificial Chromosome) Isolate Passaged in Fibroblasts To Allow Accumulation of Compensatory Mutations |
title_full_unstemmed | Complete Genome Sequence of a UL96 Mutant Cytomegalovirus Towne-BAC (Bacterial Artificial Chromosome) Isolate Passaged in Fibroblasts To Allow Accumulation of Compensatory Mutations |
title_short | Complete Genome Sequence of a UL96 Mutant Cytomegalovirus Towne-BAC (Bacterial Artificial Chromosome) Isolate Passaged in Fibroblasts To Allow Accumulation of Compensatory Mutations |
title_sort | complete genome sequence of a ul96 mutant cytomegalovirus towne-bac (bacterial artificial chromosome) isolate passaged in fibroblasts to allow accumulation of compensatory mutations |
topic | Viruses |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3813188/ https://www.ncbi.nlm.nih.gov/pubmed/24158558 http://dx.doi.org/10.1128/genomeA.00901-13 |
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