Cargando…

MicroRNA evolution, expression, and function during short germband development in Tribolium castaneum

MicroRNAs are well-established players in the development of multicellular animals. Most of our understanding of microRNA function in arthropod development comes from studies in Drosophila. Despite their advantages as model systems, the long germband embryogenesis of fruit flies is an evolutionary d...

Descripción completa

Detalles Bibliográficos
Autores principales: Ninova, Maria, Ronshaugen, Matthew, Griffiths-Jones, Sam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4691753/
https://www.ncbi.nlm.nih.gov/pubmed/26518483
http://dx.doi.org/10.1101/gr.193367.115
_version_ 1782407189128806400
author Ninova, Maria
Ronshaugen, Matthew
Griffiths-Jones, Sam
author_facet Ninova, Maria
Ronshaugen, Matthew
Griffiths-Jones, Sam
author_sort Ninova, Maria
collection PubMed
description MicroRNAs are well-established players in the development of multicellular animals. Most of our understanding of microRNA function in arthropod development comes from studies in Drosophila. Despite their advantages as model systems, the long germband embryogenesis of fruit flies is an evolutionary derived state restricted to several holometabolous insect lineages. MicroRNA evolution and expression across development in animals exhibiting the ancestral and more widespread short germband mode of embryogenesis has not been characterized. We sequenced small RNA libraries of oocytes and successive intervals covering the embryonic development of the short germband model organism, Tribolium castaneum. We analyzed the evolution and temporal expression of the microRNA complement and sequenced libraries of total RNA to investigate the relationships with microRNA target expression. We show microRNA maternal loading and sequence-specific 3′ end nontemplate oligoadenylation of maternally deposited microRNAs that is conserved between Tribolium and Drosophila. We further uncover large clusters encoding multiple paralogs from several Tribolium-specific microRNA families expressed during a narrow interval of time immediately after the activation of zygotic transcription. These novel microRNAs, together with several early expressed conserved microRNAs, target a significant number of maternally deposited transcripts. Comparison with Drosophila shows that microRNA-mediated maternal transcript targeting is a conserved process in insects, but the number and sequences of microRNAs involved have diverged. The expression of fast-evolving and species-specific microRNAs in the early blastoderm of T. castaneum is consistent with previous findings in Drosophila and shows that the unique permissiveness for microRNA innovation at this stage is a conserved phenomenon.
format Online
Article
Text
id pubmed-4691753
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Cold Spring Harbor Laboratory Press
record_format MEDLINE/PubMed
spelling pubmed-46917532016-01-08 MicroRNA evolution, expression, and function during short germband development in Tribolium castaneum Ninova, Maria Ronshaugen, Matthew Griffiths-Jones, Sam Genome Res Research MicroRNAs are well-established players in the development of multicellular animals. Most of our understanding of microRNA function in arthropod development comes from studies in Drosophila. Despite their advantages as model systems, the long germband embryogenesis of fruit flies is an evolutionary derived state restricted to several holometabolous insect lineages. MicroRNA evolution and expression across development in animals exhibiting the ancestral and more widespread short germband mode of embryogenesis has not been characterized. We sequenced small RNA libraries of oocytes and successive intervals covering the embryonic development of the short germband model organism, Tribolium castaneum. We analyzed the evolution and temporal expression of the microRNA complement and sequenced libraries of total RNA to investigate the relationships with microRNA target expression. We show microRNA maternal loading and sequence-specific 3′ end nontemplate oligoadenylation of maternally deposited microRNAs that is conserved between Tribolium and Drosophila. We further uncover large clusters encoding multiple paralogs from several Tribolium-specific microRNA families expressed during a narrow interval of time immediately after the activation of zygotic transcription. These novel microRNAs, together with several early expressed conserved microRNAs, target a significant number of maternally deposited transcripts. Comparison with Drosophila shows that microRNA-mediated maternal transcript targeting is a conserved process in insects, but the number and sequences of microRNAs involved have diverged. The expression of fast-evolving and species-specific microRNAs in the early blastoderm of T. castaneum is consistent with previous findings in Drosophila and shows that the unique permissiveness for microRNA innovation at this stage is a conserved phenomenon. Cold Spring Harbor Laboratory Press 2016-01 /pmc/articles/PMC4691753/ /pubmed/26518483 http://dx.doi.org/10.1101/gr.193367.115 Text en © 2016 Ninova et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by/4.0/ This article, published in Genome Research, is available under a Creative Commons License (Attribution 4.0 International), as described at http://creativecommons.org/licenses/by/4.0/.
spellingShingle Research
Ninova, Maria
Ronshaugen, Matthew
Griffiths-Jones, Sam
MicroRNA evolution, expression, and function during short germband development in Tribolium castaneum
title MicroRNA evolution, expression, and function during short germband development in Tribolium castaneum
title_full MicroRNA evolution, expression, and function during short germband development in Tribolium castaneum
title_fullStr MicroRNA evolution, expression, and function during short germband development in Tribolium castaneum
title_full_unstemmed MicroRNA evolution, expression, and function during short germband development in Tribolium castaneum
title_short MicroRNA evolution, expression, and function during short germband development in Tribolium castaneum
title_sort microrna evolution, expression, and function during short germband development in tribolium castaneum
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4691753/
https://www.ncbi.nlm.nih.gov/pubmed/26518483
http://dx.doi.org/10.1101/gr.193367.115
work_keys_str_mv AT ninovamaria micrornaevolutionexpressionandfunctionduringshortgermbanddevelopmentintriboliumcastaneum
AT ronshaugenmatthew micrornaevolutionexpressionandfunctionduringshortgermbanddevelopmentintriboliumcastaneum
AT griffithsjonessam micrornaevolutionexpressionandfunctionduringshortgermbanddevelopmentintriboliumcastaneum