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Small noncoding RNA profiles along alternative developmental trajectories in an annual killifish
Embryonic development of Austrofundulus limnaeus can occur along two phenotypic trajectories that are physiologically and biochemically distinct. Phenotype appears to be influenced by maternal provisioning based on the observation that young females produce predominately non-diapausing embryos and o...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6127099/ https://www.ncbi.nlm.nih.gov/pubmed/30190591 http://dx.doi.org/10.1038/s41598-018-31466-7 |
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author | Romney, Amie L. T. Podrabsky, Jason E. |
author_facet | Romney, Amie L. T. Podrabsky, Jason E. |
author_sort | Romney, Amie L. T. |
collection | PubMed |
description | Embryonic development of Austrofundulus limnaeus can occur along two phenotypic trajectories that are physiologically and biochemically distinct. Phenotype appears to be influenced by maternal provisioning based on the observation that young females produce predominately non-diapausing embryos and older females produce mostly diapausing embryos. Embryonic incubation temperature can override this pattern and alter trajectory. We hypothesized that temperature-induced phenotypic plasticity may be regulated by post-transcriptional modification via noncoding RNAs. As a first step to exploring this possibility, RNA-seq was used to generate transcriptomic profiles of small noncoding RNAs in embryos developing along the two alternative trajectories. We find distinct profiles of mature sequences belonging to the miR-10 family expressed in increasing abundance during development and mature sequences of miR-430 that follow the opposite pattern. Furthermore, miR-430 sequences are enriched in escape trajectory embryos. MiR-430 family members are known to target maternally provisioned mRNAs in zebrafish and may operate similarly in A. limnaeus in the context of normal development, and also by targeting trajectory-specific mRNAs. This expression pattern and function for miR-430 presents a potentially novel model for maternal-embryonic conflict in gene regulation that provides the embryo the ability to override maternal programming in the face of altered environmental conditions. |
format | Online Article Text |
id | pubmed-6127099 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61270992018-09-10 Small noncoding RNA profiles along alternative developmental trajectories in an annual killifish Romney, Amie L. T. Podrabsky, Jason E. Sci Rep Article Embryonic development of Austrofundulus limnaeus can occur along two phenotypic trajectories that are physiologically and biochemically distinct. Phenotype appears to be influenced by maternal provisioning based on the observation that young females produce predominately non-diapausing embryos and older females produce mostly diapausing embryos. Embryonic incubation temperature can override this pattern and alter trajectory. We hypothesized that temperature-induced phenotypic plasticity may be regulated by post-transcriptional modification via noncoding RNAs. As a first step to exploring this possibility, RNA-seq was used to generate transcriptomic profiles of small noncoding RNAs in embryos developing along the two alternative trajectories. We find distinct profiles of mature sequences belonging to the miR-10 family expressed in increasing abundance during development and mature sequences of miR-430 that follow the opposite pattern. Furthermore, miR-430 sequences are enriched in escape trajectory embryos. MiR-430 family members are known to target maternally provisioned mRNAs in zebrafish and may operate similarly in A. limnaeus in the context of normal development, and also by targeting trajectory-specific mRNAs. This expression pattern and function for miR-430 presents a potentially novel model for maternal-embryonic conflict in gene regulation that provides the embryo the ability to override maternal programming in the face of altered environmental conditions. Nature Publishing Group UK 2018-09-06 /pmc/articles/PMC6127099/ /pubmed/30190591 http://dx.doi.org/10.1038/s41598-018-31466-7 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Romney, Amie L. T. Podrabsky, Jason E. Small noncoding RNA profiles along alternative developmental trajectories in an annual killifish |
title | Small noncoding RNA profiles along alternative developmental trajectories in an annual killifish |
title_full | Small noncoding RNA profiles along alternative developmental trajectories in an annual killifish |
title_fullStr | Small noncoding RNA profiles along alternative developmental trajectories in an annual killifish |
title_full_unstemmed | Small noncoding RNA profiles along alternative developmental trajectories in an annual killifish |
title_short | Small noncoding RNA profiles along alternative developmental trajectories in an annual killifish |
title_sort | small noncoding rna profiles along alternative developmental trajectories in an annual killifish |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6127099/ https://www.ncbi.nlm.nih.gov/pubmed/30190591 http://dx.doi.org/10.1038/s41598-018-31466-7 |
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