Cargando…

The impact of age, biogenesis, and genomic clustering on Drosophila microRNA evolution

The molecular evolutionary signatures of miRNAs inform our understanding of their emergence, biogenesis, and function. The known signatures of miRNA evolution have derived mostly from the analysis of deeply conserved, canonical loci. In this study, we examine the impact of age, biogenesis pathway, a...

Descripción completa

Detalles Bibliográficos
Autores principales: Mohammed, Jaaved, Flynt, Alex S., Siepel, Adam, Lai, Eric C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3753935/
https://www.ncbi.nlm.nih.gov/pubmed/23882112
http://dx.doi.org/10.1261/rna.039248.113
_version_ 1782281892385521664
author Mohammed, Jaaved
Flynt, Alex S.
Siepel, Adam
Lai, Eric C.
author_facet Mohammed, Jaaved
Flynt, Alex S.
Siepel, Adam
Lai, Eric C.
author_sort Mohammed, Jaaved
collection PubMed
description The molecular evolutionary signatures of miRNAs inform our understanding of their emergence, biogenesis, and function. The known signatures of miRNA evolution have derived mostly from the analysis of deeply conserved, canonical loci. In this study, we examine the impact of age, biogenesis pathway, and genomic arrangement on the evolutionary properties of Drosophila miRNAs. Crucial to the accuracy of our results was our curation of high-quality miRNA alignments, which included nearly 150 corrections to ortholog calls and nucleotide sequences of the global 12-way Drosophilid alignments currently available. Using these data, we studied primary sequence conservation, normalized free-energy values, and types of structure-preserving substitutions. We expand upon common miRNA evolutionary patterns that reflect fundamental features of miRNAs that are under functional selection. We observe that melanogaster-subgroup-specific miRNAs, although recently emerged and rapidly evolving, nonetheless exhibit evolutionary signatures that are similar to well-conserved miRNAs and distinct from other structured noncoding RNAs and bulk conserved non-miRNA hairpins. This provides evidence that even young miRNAs may be selected for regulatory activities. More strikingly, we observe that mirtrons and clustered miRNAs both exhibit distinct evolutionary properties relative to solo, well-conserved miRNAs, even after controlling for sequence depth. These studies highlight the previously unappreciated impact of biogenesis strategy and genomic location on the evolutionary dynamics of miRNAs, and affirm that miRNAs do not evolve as a unitary class.
format Online
Article
Text
id pubmed-3753935
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Cold Spring Harbor Laboratory Press
record_format MEDLINE/PubMed
spelling pubmed-37539352014-09-01 The impact of age, biogenesis, and genomic clustering on Drosophila microRNA evolution Mohammed, Jaaved Flynt, Alex S. Siepel, Adam Lai, Eric C. RNA Articles The molecular evolutionary signatures of miRNAs inform our understanding of their emergence, biogenesis, and function. The known signatures of miRNA evolution have derived mostly from the analysis of deeply conserved, canonical loci. In this study, we examine the impact of age, biogenesis pathway, and genomic arrangement on the evolutionary properties of Drosophila miRNAs. Crucial to the accuracy of our results was our curation of high-quality miRNA alignments, which included nearly 150 corrections to ortholog calls and nucleotide sequences of the global 12-way Drosophilid alignments currently available. Using these data, we studied primary sequence conservation, normalized free-energy values, and types of structure-preserving substitutions. We expand upon common miRNA evolutionary patterns that reflect fundamental features of miRNAs that are under functional selection. We observe that melanogaster-subgroup-specific miRNAs, although recently emerged and rapidly evolving, nonetheless exhibit evolutionary signatures that are similar to well-conserved miRNAs and distinct from other structured noncoding RNAs and bulk conserved non-miRNA hairpins. This provides evidence that even young miRNAs may be selected for regulatory activities. More strikingly, we observe that mirtrons and clustered miRNAs both exhibit distinct evolutionary properties relative to solo, well-conserved miRNAs, even after controlling for sequence depth. These studies highlight the previously unappreciated impact of biogenesis strategy and genomic location on the evolutionary dynamics of miRNAs, and affirm that miRNAs do not evolve as a unitary class. Cold Spring Harbor Laboratory Press 2013-09 /pmc/articles/PMC3753935/ /pubmed/23882112 http://dx.doi.org/10.1261/rna.039248.113 Text en © 2013; Published by Cold Spring Harbor Laboratory Press for the RNA Society http://creativecommons.org/licenses/by-nc/3.0/ This article is distributed exclusively by the RNA Society for the first 12 months after the full-issue publication date (see http://rnajournal.cshlp.org/site/misc/terms.xhtml). After 12 months, it is available under a Creative Commons License (Attribution-NonCommercial 3.0 Unported), as described at http://creativecommons.org/licenses/by-nc/3.0/.
spellingShingle Articles
Mohammed, Jaaved
Flynt, Alex S.
Siepel, Adam
Lai, Eric C.
The impact of age, biogenesis, and genomic clustering on Drosophila microRNA evolution
title The impact of age, biogenesis, and genomic clustering on Drosophila microRNA evolution
title_full The impact of age, biogenesis, and genomic clustering on Drosophila microRNA evolution
title_fullStr The impact of age, biogenesis, and genomic clustering on Drosophila microRNA evolution
title_full_unstemmed The impact of age, biogenesis, and genomic clustering on Drosophila microRNA evolution
title_short The impact of age, biogenesis, and genomic clustering on Drosophila microRNA evolution
title_sort impact of age, biogenesis, and genomic clustering on drosophila microrna evolution
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3753935/
https://www.ncbi.nlm.nih.gov/pubmed/23882112
http://dx.doi.org/10.1261/rna.039248.113
work_keys_str_mv AT mohammedjaaved theimpactofagebiogenesisandgenomicclusteringondrosophilamicrornaevolution
AT flyntalexs theimpactofagebiogenesisandgenomicclusteringondrosophilamicrornaevolution
AT siepeladam theimpactofagebiogenesisandgenomicclusteringondrosophilamicrornaevolution
AT laiericc theimpactofagebiogenesisandgenomicclusteringondrosophilamicrornaevolution
AT mohammedjaaved impactofagebiogenesisandgenomicclusteringondrosophilamicrornaevolution
AT flyntalexs impactofagebiogenesisandgenomicclusteringondrosophilamicrornaevolution
AT siepeladam impactofagebiogenesisandgenomicclusteringondrosophilamicrornaevolution
AT laiericc impactofagebiogenesisandgenomicclusteringondrosophilamicrornaevolution