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Investigating the origin of subtelomeric and centromeric AT-rich elements in Aspergillus flavus
An in silico study of Aspergillus flavus genome stability uncovered significant variations in both coding and non-coding regions. The non-coding insertions uniformly consisted of AT-rich sequences that are evolutionarily maintained, albeit distributed at widely different sites in an array of A. flav...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9910759/ https://www.ncbi.nlm.nih.gov/pubmed/36758027 http://dx.doi.org/10.1371/journal.pone.0279148 |
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author | Lustig, Arthur J. |
author_facet | Lustig, Arthur J. |
author_sort | Lustig, Arthur J. |
collection | PubMed |
description | An in silico study of Aspergillus flavus genome stability uncovered significant variations in both coding and non-coding regions. The non-coding insertions uniformly consisted of AT-rich sequences that are evolutionarily maintained, albeit distributed at widely different sites in an array of A. flavus strains. A survey of ≥ 2kb AT-rich elements (AT ≥ 70%; ATEs) in non-centromeric regions uncovered two major categories of ATEs. The first category is composed of homologous insertions at ectopic, non-allelic sites that contain homology to transposable elements (TEs; Classes B, C, D, and E). Strains differed significantly in frequency, position, and TE type, but displayed a common enrichment in subtelomeric regions. The TEs were heavily mutated, with patterns consistent with the ancestral activity of repeat-induced point mutations (RIP). The second category consists of a conserved set of novel subtelomeric ATE repeats (Classes A, G, G, H, I and J) which lack discernible TEs and, unlike TEs, display a constant polarity relative to the telomere. Members of one of these classes are derivatives of a progenitor ATE that is predicted to have undergone extensive homologous recombination during evolution. A third category of ATEs consists of ~100 kb regions at each centromere. Centromeric ATEs and TE clusters within these centromeres display a high level of sequence identity between strains. These studies suggest that transposition and RIP are forces in the evolution of subtelomeric and centromeric structure and function. |
format | Online Article Text |
id | pubmed-9910759 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-99107592023-02-10 Investigating the origin of subtelomeric and centromeric AT-rich elements in Aspergillus flavus Lustig, Arthur J. PLoS One Research Article An in silico study of Aspergillus flavus genome stability uncovered significant variations in both coding and non-coding regions. The non-coding insertions uniformly consisted of AT-rich sequences that are evolutionarily maintained, albeit distributed at widely different sites in an array of A. flavus strains. A survey of ≥ 2kb AT-rich elements (AT ≥ 70%; ATEs) in non-centromeric regions uncovered two major categories of ATEs. The first category is composed of homologous insertions at ectopic, non-allelic sites that contain homology to transposable elements (TEs; Classes B, C, D, and E). Strains differed significantly in frequency, position, and TE type, but displayed a common enrichment in subtelomeric regions. The TEs were heavily mutated, with patterns consistent with the ancestral activity of repeat-induced point mutations (RIP). The second category consists of a conserved set of novel subtelomeric ATE repeats (Classes A, G, G, H, I and J) which lack discernible TEs and, unlike TEs, display a constant polarity relative to the telomere. Members of one of these classes are derivatives of a progenitor ATE that is predicted to have undergone extensive homologous recombination during evolution. A third category of ATEs consists of ~100 kb regions at each centromere. Centromeric ATEs and TE clusters within these centromeres display a high level of sequence identity between strains. These studies suggest that transposition and RIP are forces in the evolution of subtelomeric and centromeric structure and function. Public Library of Science 2023-02-09 /pmc/articles/PMC9910759/ /pubmed/36758027 http://dx.doi.org/10.1371/journal.pone.0279148 Text en © 2023 Arthur J. Lustig https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://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 Lustig, Arthur J. Investigating the origin of subtelomeric and centromeric AT-rich elements in Aspergillus flavus |
title | Investigating the origin of subtelomeric and centromeric AT-rich elements in Aspergillus flavus |
title_full | Investigating the origin of subtelomeric and centromeric AT-rich elements in Aspergillus flavus |
title_fullStr | Investigating the origin of subtelomeric and centromeric AT-rich elements in Aspergillus flavus |
title_full_unstemmed | Investigating the origin of subtelomeric and centromeric AT-rich elements in Aspergillus flavus |
title_short | Investigating the origin of subtelomeric and centromeric AT-rich elements in Aspergillus flavus |
title_sort | investigating the origin of subtelomeric and centromeric at-rich elements in aspergillus flavus |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9910759/ https://www.ncbi.nlm.nih.gov/pubmed/36758027 http://dx.doi.org/10.1371/journal.pone.0279148 |
work_keys_str_mv | AT lustigarthurj investigatingtheoriginofsubtelomericandcentromericatrichelementsinaspergillusflavus |