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DNA sequence elements required for partitioning competence of the Saccharomyces cerevisiae 2-micron plasmid STB locus
Equal partitioning of the multi-copy yeast 2-micron plasmid requires association of plasmid proteins Rep1 and Rep2 with tandem repeats at the plasmid STB locus. To identify sequence elements required for these associations we generated synthetic versions of a 63-bp section of STB, encompassing one r...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6344848/ https://www.ncbi.nlm.nih.gov/pubmed/30445476 http://dx.doi.org/10.1093/nar/gky1150 |
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author | McQuaid, Mary E Polvi, Elizabeth J Dobson, Melanie J |
author_facet | McQuaid, Mary E Polvi, Elizabeth J Dobson, Melanie J |
author_sort | McQuaid, Mary E |
collection | PubMed |
description | Equal partitioning of the multi-copy yeast 2-micron plasmid requires association of plasmid proteins Rep1 and Rep2 with tandem repeats at the plasmid STB locus. To identify sequence elements required for these associations we generated synthetic versions of a 63-bp section of STB, encompassing one repeat. A single copy of this sequence was sufficient for Rep protein association in vivo, while two directly arrayed copies provided partitioning function to a plasmid lacking all other 2-micron sequences. Partitioning efficiency increased with increasing repeat number, reaching that conferred by the native STB repeat array. By altering sequences in synthetic repeats, we identified the TGCA component of a TGCATTTTT motif as critical for Rep protein recognition, with a second TGCA sequence in each repeat also contributing to association. Mutation of TGCATTTTT to TGTATTTT, as found in variant 2-micron STB repeats, also allowed Rep protein association, while mutation to TGCATTAAT impaired inheritance without abolishing Rep protein recognition, suggesting an alternate role for the T-tract. Our identification of sequence motifs required for Rep protein recognition provides the basis for understanding higher-order Rep protein arrangements at STB that enable the yeast 2-micron plasmid to be efficiently partitioned during host cell division. |
format | Online Article Text |
id | pubmed-6344848 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-63448482019-01-29 DNA sequence elements required for partitioning competence of the Saccharomyces cerevisiae 2-micron plasmid STB locus McQuaid, Mary E Polvi, Elizabeth J Dobson, Melanie J Nucleic Acids Res Gene regulation, Chromatin and Epigenetics Equal partitioning of the multi-copy yeast 2-micron plasmid requires association of plasmid proteins Rep1 and Rep2 with tandem repeats at the plasmid STB locus. To identify sequence elements required for these associations we generated synthetic versions of a 63-bp section of STB, encompassing one repeat. A single copy of this sequence was sufficient for Rep protein association in vivo, while two directly arrayed copies provided partitioning function to a plasmid lacking all other 2-micron sequences. Partitioning efficiency increased with increasing repeat number, reaching that conferred by the native STB repeat array. By altering sequences in synthetic repeats, we identified the TGCA component of a TGCATTTTT motif as critical for Rep protein recognition, with a second TGCA sequence in each repeat also contributing to association. Mutation of TGCATTTTT to TGTATTTT, as found in variant 2-micron STB repeats, also allowed Rep protein association, while mutation to TGCATTAAT impaired inheritance without abolishing Rep protein recognition, suggesting an alternate role for the T-tract. Our identification of sequence motifs required for Rep protein recognition provides the basis for understanding higher-order Rep protein arrangements at STB that enable the yeast 2-micron plasmid to be efficiently partitioned during host cell division. Oxford University Press 2019-01-25 2018-11-16 /pmc/articles/PMC6344848/ /pubmed/30445476 http://dx.doi.org/10.1093/nar/gky1150 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Gene regulation, Chromatin and Epigenetics McQuaid, Mary E Polvi, Elizabeth J Dobson, Melanie J DNA sequence elements required for partitioning competence of the Saccharomyces cerevisiae 2-micron plasmid STB locus |
title | DNA sequence elements required for partitioning competence of the Saccharomyces cerevisiae 2-micron plasmid STB locus |
title_full | DNA sequence elements required for partitioning competence of the Saccharomyces cerevisiae 2-micron plasmid STB locus |
title_fullStr | DNA sequence elements required for partitioning competence of the Saccharomyces cerevisiae 2-micron plasmid STB locus |
title_full_unstemmed | DNA sequence elements required for partitioning competence of the Saccharomyces cerevisiae 2-micron plasmid STB locus |
title_short | DNA sequence elements required for partitioning competence of the Saccharomyces cerevisiae 2-micron plasmid STB locus |
title_sort | dna sequence elements required for partitioning competence of the saccharomyces cerevisiae 2-micron plasmid stb locus |
topic | Gene regulation, Chromatin and Epigenetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6344848/ https://www.ncbi.nlm.nih.gov/pubmed/30445476 http://dx.doi.org/10.1093/nar/gky1150 |
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