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A de novo transcriptional atlas in Danaus plexippus reveals variability in dosage compensation across tissues

A detailed knowledge of gene function in the monarch butterfly is still lacking. Here we generate a genome assembly from a Mexican nonmigratory population and used RNA-seq data from 14 biological samples for gene annotation and to construct an atlas portraying the breadth of gene expression during m...

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Autores principales: Ranz, José M., González, Pablo M., Clifton, Bryan D., Nazario-Yepiz, Nestor O., Hernández-Cervantes, Pablo L., Palma-Martínez, María J., Valdivia, Dulce I., Jiménez-Kaufman, Andrés, Lu, Megan M., Markow, Therese A., Abreu-Goodger, Cei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8233437/
https://www.ncbi.nlm.nih.gov/pubmed/34172835
http://dx.doi.org/10.1038/s42003-021-02335-3
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author Ranz, José M.
González, Pablo M.
Clifton, Bryan D.
Nazario-Yepiz, Nestor O.
Hernández-Cervantes, Pablo L.
Palma-Martínez, María J.
Valdivia, Dulce I.
Jiménez-Kaufman, Andrés
Lu, Megan M.
Markow, Therese A.
Abreu-Goodger, Cei
author_facet Ranz, José M.
González, Pablo M.
Clifton, Bryan D.
Nazario-Yepiz, Nestor O.
Hernández-Cervantes, Pablo L.
Palma-Martínez, María J.
Valdivia, Dulce I.
Jiménez-Kaufman, Andrés
Lu, Megan M.
Markow, Therese A.
Abreu-Goodger, Cei
author_sort Ranz, José M.
collection PubMed
description A detailed knowledge of gene function in the monarch butterfly is still lacking. Here we generate a genome assembly from a Mexican nonmigratory population and used RNA-seq data from 14 biological samples for gene annotation and to construct an atlas portraying the breadth of gene expression during most of the monarch life cycle. Two thirds of the genes show expression changes, with long noncoding RNAs being particularly finely regulated during adulthood, and male-biased expression being four times more common than female-biased. The two portions of the monarch heterochromosome Z, one ancestral to the Lepidoptera and the other resulting from a chromosomal fusion, display distinct association with sex-biased expression, reflecting sample-dependent incompleteness or absence of dosage compensation in the ancestral but not the novel portion of the Z. This study presents extended genomic and transcriptomic resources that will facilitate a better understanding of the monarch’s adaptation to a changing environment.
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spelling pubmed-82334372021-07-09 A de novo transcriptional atlas in Danaus plexippus reveals variability in dosage compensation across tissues Ranz, José M. González, Pablo M. Clifton, Bryan D. Nazario-Yepiz, Nestor O. Hernández-Cervantes, Pablo L. Palma-Martínez, María J. Valdivia, Dulce I. Jiménez-Kaufman, Andrés Lu, Megan M. Markow, Therese A. Abreu-Goodger, Cei Commun Biol Article A detailed knowledge of gene function in the monarch butterfly is still lacking. Here we generate a genome assembly from a Mexican nonmigratory population and used RNA-seq data from 14 biological samples for gene annotation and to construct an atlas portraying the breadth of gene expression during most of the monarch life cycle. Two thirds of the genes show expression changes, with long noncoding RNAs being particularly finely regulated during adulthood, and male-biased expression being four times more common than female-biased. The two portions of the monarch heterochromosome Z, one ancestral to the Lepidoptera and the other resulting from a chromosomal fusion, display distinct association with sex-biased expression, reflecting sample-dependent incompleteness or absence of dosage compensation in the ancestral but not the novel portion of the Z. This study presents extended genomic and transcriptomic resources that will facilitate a better understanding of the monarch’s adaptation to a changing environment. Nature Publishing Group UK 2021-06-25 /pmc/articles/PMC8233437/ /pubmed/34172835 http://dx.doi.org/10.1038/s42003-021-02335-3 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Ranz, José M.
González, Pablo M.
Clifton, Bryan D.
Nazario-Yepiz, Nestor O.
Hernández-Cervantes, Pablo L.
Palma-Martínez, María J.
Valdivia, Dulce I.
Jiménez-Kaufman, Andrés
Lu, Megan M.
Markow, Therese A.
Abreu-Goodger, Cei
A de novo transcriptional atlas in Danaus plexippus reveals variability in dosage compensation across tissues
title A de novo transcriptional atlas in Danaus plexippus reveals variability in dosage compensation across tissues
title_full A de novo transcriptional atlas in Danaus plexippus reveals variability in dosage compensation across tissues
title_fullStr A de novo transcriptional atlas in Danaus plexippus reveals variability in dosage compensation across tissues
title_full_unstemmed A de novo transcriptional atlas in Danaus plexippus reveals variability in dosage compensation across tissues
title_short A de novo transcriptional atlas in Danaus plexippus reveals variability in dosage compensation across tissues
title_sort de novo transcriptional atlas in danaus plexippus reveals variability in dosage compensation across tissues
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8233437/
https://www.ncbi.nlm.nih.gov/pubmed/34172835
http://dx.doi.org/10.1038/s42003-021-02335-3
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