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Where the minor things are: a pan-eukaryotic survey suggests neutral processes may explain much of minor intron evolution
Spliceosomal introns are gene segments removed from RNA transcripts by ribonucleoprotein machineries called spliceosomes. In some eukaryotes a second ‘minor’ spliceosome is responsible for processing a tiny minority of introns. Despite its seemingly modest role, minor splicing has persisted for roug...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10639083/ https://www.ncbi.nlm.nih.gov/pubmed/37819006 http://dx.doi.org/10.1093/nar/gkad797 |
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author | Larue, Graham E Roy, Scott W |
author_facet | Larue, Graham E Roy, Scott W |
author_sort | Larue, Graham E |
collection | PubMed |
description | Spliceosomal introns are gene segments removed from RNA transcripts by ribonucleoprotein machineries called spliceosomes. In some eukaryotes a second ‘minor’ spliceosome is responsible for processing a tiny minority of introns. Despite its seemingly modest role, minor splicing has persisted for roughly 1.5 billion years of eukaryotic evolution. Identifying minor introns in over 3000 eukaryotic genomes, we report diverse evolutionary histories including surprisingly high numbers in some fungi and green algae, repeated loss, as well as general biases in their positional and genic distributions. We estimate that ancestral minor intron densities were comparable to those of vertebrates, suggesting a trend of long-term stasis. Finally, three findings suggest a major role for neutral processes in minor intron evolution. First, highly similar patterns of minor and major intron evolution contrast with both functionalist and deleterious model predictions. Second, observed functional biases among minor intron-containing genes are largely explained by these genes’ greater ages. Third, no association of intron splicing with cell proliferation in a minor intron-rich fungus suggests that regulatory roles are lineage-specific and thus cannot offer a general explanation for minor splicing’s persistence. These data constitute the most comprehensive view of minor introns and their evolutionary history to date, and provide a foundation for future studies of these remarkable genetic elements. |
format | Online Article Text |
id | pubmed-10639083 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-106390832023-11-15 Where the minor things are: a pan-eukaryotic survey suggests neutral processes may explain much of minor intron evolution Larue, Graham E Roy, Scott W Nucleic Acids Res Computational Biology Spliceosomal introns are gene segments removed from RNA transcripts by ribonucleoprotein machineries called spliceosomes. In some eukaryotes a second ‘minor’ spliceosome is responsible for processing a tiny minority of introns. Despite its seemingly modest role, minor splicing has persisted for roughly 1.5 billion years of eukaryotic evolution. Identifying minor introns in over 3000 eukaryotic genomes, we report diverse evolutionary histories including surprisingly high numbers in some fungi and green algae, repeated loss, as well as general biases in their positional and genic distributions. We estimate that ancestral minor intron densities were comparable to those of vertebrates, suggesting a trend of long-term stasis. Finally, three findings suggest a major role for neutral processes in minor intron evolution. First, highly similar patterns of minor and major intron evolution contrast with both functionalist and deleterious model predictions. Second, observed functional biases among minor intron-containing genes are largely explained by these genes’ greater ages. Third, no association of intron splicing with cell proliferation in a minor intron-rich fungus suggests that regulatory roles are lineage-specific and thus cannot offer a general explanation for minor splicing’s persistence. These data constitute the most comprehensive view of minor introns and their evolutionary history to date, and provide a foundation for future studies of these remarkable genetic elements. Oxford University Press 2023-10-11 /pmc/articles/PMC10639083/ /pubmed/37819006 http://dx.doi.org/10.1093/nar/gkad797 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Nucleic Acids Research. 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Computational Biology Larue, Graham E Roy, Scott W Where the minor things are: a pan-eukaryotic survey suggests neutral processes may explain much of minor intron evolution |
title | Where the minor things are: a pan-eukaryotic survey suggests neutral processes may explain much of minor intron evolution |
title_full | Where the minor things are: a pan-eukaryotic survey suggests neutral processes may explain much of minor intron evolution |
title_fullStr | Where the minor things are: a pan-eukaryotic survey suggests neutral processes may explain much of minor intron evolution |
title_full_unstemmed | Where the minor things are: a pan-eukaryotic survey suggests neutral processes may explain much of minor intron evolution |
title_short | Where the minor things are: a pan-eukaryotic survey suggests neutral processes may explain much of minor intron evolution |
title_sort | where the minor things are: a pan-eukaryotic survey suggests neutral processes may explain much of minor intron evolution |
topic | Computational Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10639083/ https://www.ncbi.nlm.nih.gov/pubmed/37819006 http://dx.doi.org/10.1093/nar/gkad797 |
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