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Most synonymous allelic variants in HIV tat are not silent

The genetic code has degenerate codons that produce no change in the translated protein sequence and are generally thought to be silent. However, some synonymous variants are clearly not silent. Herein, we questioned the frequency of non-silent synonymous variants. We tested how random synonymous va...

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Autores principales: Giacoletto, Christopher J., Benjamin, Ronald, Deng, Hong-Wen, Rotter, Jerome I., Schiller, Martin R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10257815/
https://www.ncbi.nlm.nih.gov/pubmed/36893872
http://dx.doi.org/10.1016/j.ygeno.2023.110603
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author Giacoletto, Christopher J.
Benjamin, Ronald
Deng, Hong-Wen
Rotter, Jerome I.
Schiller, Martin R.
author_facet Giacoletto, Christopher J.
Benjamin, Ronald
Deng, Hong-Wen
Rotter, Jerome I.
Schiller, Martin R.
author_sort Giacoletto, Christopher J.
collection PubMed
description The genetic code has degenerate codons that produce no change in the translated protein sequence and are generally thought to be silent. However, some synonymous variants are clearly not silent. Herein, we questioned the frequency of non-silent synonymous variants. We tested how random synonymous variants in the HIV Tat transcription factor effect transcription of an LTR-GFP reporter. Our model system has the advantage of directly measuring the function of the gene in human cells. Approximately, 67% of synonymous variants in Tat were non-silent, either having reduced activity or were full loss-of-function alleles. Eight mutant codons had higher codon usage than wild type, accompanied by reduced transcriptional activity. These were clustered on a loop in the Tat structure. We conclude that most synonymous Tat variants are not silent in human cells, and 25% are associated with changes in codon usage, likely effecting protein folding.
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spelling pubmed-102578152023-06-11 Most synonymous allelic variants in HIV tat are not silent Giacoletto, Christopher J. Benjamin, Ronald Deng, Hong-Wen Rotter, Jerome I. Schiller, Martin R. Genomics Article The genetic code has degenerate codons that produce no change in the translated protein sequence and are generally thought to be silent. However, some synonymous variants are clearly not silent. Herein, we questioned the frequency of non-silent synonymous variants. We tested how random synonymous variants in the HIV Tat transcription factor effect transcription of an LTR-GFP reporter. Our model system has the advantage of directly measuring the function of the gene in human cells. Approximately, 67% of synonymous variants in Tat were non-silent, either having reduced activity or were full loss-of-function alleles. Eight mutant codons had higher codon usage than wild type, accompanied by reduced transcriptional activity. These were clustered on a loop in the Tat structure. We conclude that most synonymous Tat variants are not silent in human cells, and 25% are associated with changes in codon usage, likely effecting protein folding. 2023-05 2023-03-07 /pmc/articles/PMC10257815/ /pubmed/36893872 http://dx.doi.org/10.1016/j.ygeno.2023.110603 Text en https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ).
spellingShingle Article
Giacoletto, Christopher J.
Benjamin, Ronald
Deng, Hong-Wen
Rotter, Jerome I.
Schiller, Martin R.
Most synonymous allelic variants in HIV tat are not silent
title Most synonymous allelic variants in HIV tat are not silent
title_full Most synonymous allelic variants in HIV tat are not silent
title_fullStr Most synonymous allelic variants in HIV tat are not silent
title_full_unstemmed Most synonymous allelic variants in HIV tat are not silent
title_short Most synonymous allelic variants in HIV tat are not silent
title_sort most synonymous allelic variants in hiv tat are not silent
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10257815/
https://www.ncbi.nlm.nih.gov/pubmed/36893872
http://dx.doi.org/10.1016/j.ygeno.2023.110603
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