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Selection for ancient periodic motifs that do not impart DNA bending
A ~10–11 bp periodicity in dinucleotides imparting DNA bending, with shorter periods found in organisms with positively-supercoiled DNA and longer periods found in organisms with negatively-supercoiled DNA, was previously suggested to assist in DNA compaction. However, when measured with more robust...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7537859/ https://www.ncbi.nlm.nih.gov/pubmed/33022009 http://dx.doi.org/10.1371/journal.pgen.1009042 |
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author | Atzinger, Aletheia Lawrence, Jeffrey G. |
author_facet | Atzinger, Aletheia Lawrence, Jeffrey G. |
author_sort | Atzinger, Aletheia |
collection | PubMed |
description | A ~10–11 bp periodicity in dinucleotides imparting DNA bending, with shorter periods found in organisms with positively-supercoiled DNA and longer periods found in organisms with negatively-supercoiled DNA, was previously suggested to assist in DNA compaction. However, when measured with more robust methods, variation in the observed periods between organisms with different growth temperatures is not consistent with that hypothesis. We demonstrate that dinucleotide periodicity does not arise solely by mutational biases but is under selection. We found variation between genomes in both the period and the suite of dinucleotides that are periodic. Whereas organisms with similar growth temperatures have highly variable periods, differences in periods increase with phylogenetic distance between organisms. In addition, while the suites of dinucleotides under selection for periodicity become more dissimilar among more distantly-related organisms, there is a core set of dinucleotides that are strongly periodic among genomes in all domains of life. Notably, this core set of periodic motifs are not involved in DNA bending. These data indicate that dinucleotide periodicity is an ancient genomic architecture which may play a role in shaping the evolution of genes and genomes. |
format | Online Article Text |
id | pubmed-7537859 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-75378592020-10-15 Selection for ancient periodic motifs that do not impart DNA bending Atzinger, Aletheia Lawrence, Jeffrey G. PLoS Genet Research Article A ~10–11 bp periodicity in dinucleotides imparting DNA bending, with shorter periods found in organisms with positively-supercoiled DNA and longer periods found in organisms with negatively-supercoiled DNA, was previously suggested to assist in DNA compaction. However, when measured with more robust methods, variation in the observed periods between organisms with different growth temperatures is not consistent with that hypothesis. We demonstrate that dinucleotide periodicity does not arise solely by mutational biases but is under selection. We found variation between genomes in both the period and the suite of dinucleotides that are periodic. Whereas organisms with similar growth temperatures have highly variable periods, differences in periods increase with phylogenetic distance between organisms. In addition, while the suites of dinucleotides under selection for periodicity become more dissimilar among more distantly-related organisms, there is a core set of dinucleotides that are strongly periodic among genomes in all domains of life. Notably, this core set of periodic motifs are not involved in DNA bending. These data indicate that dinucleotide periodicity is an ancient genomic architecture which may play a role in shaping the evolution of genes and genomes. Public Library of Science 2020-10-06 /pmc/articles/PMC7537859/ /pubmed/33022009 http://dx.doi.org/10.1371/journal.pgen.1009042 Text en © 2020 Atzinger, Lawrence http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Atzinger, Aletheia Lawrence, Jeffrey G. Selection for ancient periodic motifs that do not impart DNA bending |
title | Selection for ancient periodic motifs that do not impart DNA bending |
title_full | Selection for ancient periodic motifs that do not impart DNA bending |
title_fullStr | Selection for ancient periodic motifs that do not impart DNA bending |
title_full_unstemmed | Selection for ancient periodic motifs that do not impart DNA bending |
title_short | Selection for ancient periodic motifs that do not impart DNA bending |
title_sort | selection for ancient periodic motifs that do not impart dna bending |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7537859/ https://www.ncbi.nlm.nih.gov/pubmed/33022009 http://dx.doi.org/10.1371/journal.pgen.1009042 |
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