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Intron dynamics reveal principles of gene regulation during the maternal-to-zygotic transition

The maternal-to-zygotic transition (MZT) is a conserved embryonic process in animals where developmental control shifts from the maternal to zygotic genome. A key step in this transition is zygotic transcription, and deciphering the MZT requires classifying newly transcribed genes. However, due to c...

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Detalles Bibliográficos
Autores principales: Riemondy, Kent, Henriksen, Jesslyn C., Rissland, Olivia S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10158999/
https://www.ncbi.nlm.nih.gov/pubmed/36764816
http://dx.doi.org/10.1261/rna.079168.122
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author Riemondy, Kent
Henriksen, Jesslyn C.
Rissland, Olivia S.
author_facet Riemondy, Kent
Henriksen, Jesslyn C.
Rissland, Olivia S.
author_sort Riemondy, Kent
collection PubMed
description The maternal-to-zygotic transition (MZT) is a conserved embryonic process in animals where developmental control shifts from the maternal to zygotic genome. A key step in this transition is zygotic transcription, and deciphering the MZT requires classifying newly transcribed genes. However, due to current technological limitations, this starting point remains a challenge for studying many species. Here, we present an alternative approach that characterizes transcriptome changes based solely on RNA-seq data. By combining intron-mapping reads and transcript-level quantification, we characterized transcriptome dynamics during the Drosophila melanogaster MZT. Our approach provides an accessible platform to investigate transcriptome dynamics that can be applied to the MZT in nonmodel organisms. In addition to classifying zygotically transcribed genes, our analysis revealed that over 300 genes express different maternal and zygotic transcript isoforms due to alternative splicing, polyadenylation, and promoter usage. The vast majority of these zygotic isoforms have the potential to be subject to different regulatory control, and over two-thirds encode different proteins. Thus, our analysis reveals an additional layer of regulation during the MZT, where new zygotic transcripts can generate additional proteome diversity.
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spelling pubmed-101589992023-05-05 Intron dynamics reveal principles of gene regulation during the maternal-to-zygotic transition Riemondy, Kent Henriksen, Jesslyn C. Rissland, Olivia S. RNA Bioinformatics The maternal-to-zygotic transition (MZT) is a conserved embryonic process in animals where developmental control shifts from the maternal to zygotic genome. A key step in this transition is zygotic transcription, and deciphering the MZT requires classifying newly transcribed genes. However, due to current technological limitations, this starting point remains a challenge for studying many species. Here, we present an alternative approach that characterizes transcriptome changes based solely on RNA-seq data. By combining intron-mapping reads and transcript-level quantification, we characterized transcriptome dynamics during the Drosophila melanogaster MZT. Our approach provides an accessible platform to investigate transcriptome dynamics that can be applied to the MZT in nonmodel organisms. In addition to classifying zygotically transcribed genes, our analysis revealed that over 300 genes express different maternal and zygotic transcript isoforms due to alternative splicing, polyadenylation, and promoter usage. The vast majority of these zygotic isoforms have the potential to be subject to different regulatory control, and over two-thirds encode different proteins. Thus, our analysis reveals an additional layer of regulation during the MZT, where new zygotic transcripts can generate additional proteome diversity. Cold Spring Harbor Laboratory Press 2023-05 /pmc/articles/PMC10158999/ /pubmed/36764816 http://dx.doi.org/10.1261/rna.079168.122 Text en © 2023 Riemondy et al.; Published by Cold Spring Harbor Laboratory Press for the RNA Society https://creativecommons.org/licenses/by-nc/4.0/This article, published in RNA, is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Bioinformatics
Riemondy, Kent
Henriksen, Jesslyn C.
Rissland, Olivia S.
Intron dynamics reveal principles of gene regulation during the maternal-to-zygotic transition
title Intron dynamics reveal principles of gene regulation during the maternal-to-zygotic transition
title_full Intron dynamics reveal principles of gene regulation during the maternal-to-zygotic transition
title_fullStr Intron dynamics reveal principles of gene regulation during the maternal-to-zygotic transition
title_full_unstemmed Intron dynamics reveal principles of gene regulation during the maternal-to-zygotic transition
title_short Intron dynamics reveal principles of gene regulation during the maternal-to-zygotic transition
title_sort intron dynamics reveal principles of gene regulation during the maternal-to-zygotic transition
topic Bioinformatics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10158999/
https://www.ncbi.nlm.nih.gov/pubmed/36764816
http://dx.doi.org/10.1261/rna.079168.122
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