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


Journal

Communications biology
ISSN: 2399-3642
Titre abrégé: Commun Biol
Pays: England
ID NLM: 101719179

Informations de publication

Date de publication:
25 06 2021
Historique:
received: 11 12 2020
accepted: 09 06 2021
entrez: 26 6 2021
pubmed: 27 6 2021
medline: 17 8 2021
Statut: epublish

Résumé

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.

Identifiants

pubmed: 34172835
doi: 10.1038/s42003-021-02335-3
pii: 10.1038/s42003-021-02335-3
pmc: PMC8233437
doi:

Substances chimiques

RNA, Long Noncoding 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

791

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Auteurs

José M Ranz (JM)

Department of Ecology and Evolutionary Biology, University of California Irvine, Irvine, CA, USA. jranz@uci.edu.

Pablo M González (PM)

Unidad de Genómica Avanzada (Langebio), CINVESTAV, Irapuato, GTO, Mexico.
Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, UK.

Bryan D Clifton (BD)

Department of Ecology and Evolutionary Biology, University of California Irvine, Irvine, CA, USA.

Nestor O Nazario-Yepiz (NO)

Unidad de Genómica Avanzada (Langebio), CINVESTAV, Irapuato, GTO, Mexico.

Pablo L Hernández-Cervantes (PL)

Unidad de Genómica Avanzada (Langebio), CINVESTAV, Irapuato, GTO, Mexico.

María J Palma-Martínez (MJ)

Unidad de Genómica Avanzada (Langebio), CINVESTAV, Irapuato, GTO, Mexico.

Dulce I Valdivia (DI)

Unidad de Genómica Avanzada (Langebio), CINVESTAV, Irapuato, GTO, Mexico.

Andrés Jiménez-Kaufman (A)

Unidad de Genómica Avanzada (Langebio), CINVESTAV, Irapuato, GTO, Mexico.

Megan M Lu (MM)

Department of Ecology and Evolutionary Biology, University of California Irvine, Irvine, CA, USA.

Therese A Markow (TA)

Unidad de Genómica Avanzada (Langebio), CINVESTAV, Irapuato, GTO, Mexico.
Section of Cell and Developmental Biology, Division of Biological Sciences, University of California San Diego, La Jolla, CA, USA.

Cei Abreu-Goodger (C)

Unidad de Genómica Avanzada (Langebio), CINVESTAV, Irapuato, GTO, Mexico. cei.abreu@cinvestav.mx.
Institute of Evolutionary Biology, School of Biological Sciences, University of Edinburgh, Edinburgh, UK. cei.abreu@cinvestav.mx.

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