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Widespread sex-dimorphism across single-cell transcriptomes of adult African turquoise killifish tissues

The African turquoise killifish (Nothobranchius furzeri), the shortest-lived vertebrate that can be bred in captivity, is an emerging model organism to study vertebrate aging. Here we describe the first multi-tissue, single-cell gene expression atlas of female and male turquoise killifish tissues co...

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Autores principales: Teefy, Bryan B., Lemus, Aaron J.J., Adler, Ari, Xu, Alan, Bhala, Rajyk, Hsu, Katelyn, Benayoun, Bérénice A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10197525/
https://www.ncbi.nlm.nih.gov/pubmed/37214847
http://dx.doi.org/10.1101/2023.05.05.539616
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author Teefy, Bryan B.
Lemus, Aaron J.J.
Adler, Ari
Xu, Alan
Bhala, Rajyk
Hsu, Katelyn
Benayoun, Bérénice A.
author_facet Teefy, Bryan B.
Lemus, Aaron J.J.
Adler, Ari
Xu, Alan
Bhala, Rajyk
Hsu, Katelyn
Benayoun, Bérénice A.
author_sort Teefy, Bryan B.
collection PubMed
description The African turquoise killifish (Nothobranchius furzeri), the shortest-lived vertebrate that can be bred in captivity, is an emerging model organism to study vertebrate aging. Here we describe the first multi-tissue, single-cell gene expression atlas of female and male turquoise killifish tissues comprising immune and metabolic cells from the blood, kidney, liver, and spleen. We were able to annotate 22 distinct cell types, define associated marker genes, and infer differentiation trajectories. Using this dataset, we found pervasive sex-dimorphic gene expression across cell types, especially in the liver. Sex-dimorphic genes tended to be involved in processes related to lipid metabolism, and indeed, we observed clear differences in lipid storage in female vs. male turquoise killifish livers. Importantly, we use machine-learning to predict sex using single-cell gene expression in our atlas and identify potential transcriptional markers for molecular sex identity in this species. As proof-of-principle, we show that our atlas can be used to deconvolute existing liver bulk RNA-seq data in this species to obtain accurate estimates of cell type proportions across biological conditions. We believe that this single-cell atlas can be a resource to the community that could notably be leveraged to identify cell type-specific genes for cell type-specific expression in transgenic animals.
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spelling pubmed-101975252023-05-20 Widespread sex-dimorphism across single-cell transcriptomes of adult African turquoise killifish tissues Teefy, Bryan B. Lemus, Aaron J.J. Adler, Ari Xu, Alan Bhala, Rajyk Hsu, Katelyn Benayoun, Bérénice A. bioRxiv Article The African turquoise killifish (Nothobranchius furzeri), the shortest-lived vertebrate that can be bred in captivity, is an emerging model organism to study vertebrate aging. Here we describe the first multi-tissue, single-cell gene expression atlas of female and male turquoise killifish tissues comprising immune and metabolic cells from the blood, kidney, liver, and spleen. We were able to annotate 22 distinct cell types, define associated marker genes, and infer differentiation trajectories. Using this dataset, we found pervasive sex-dimorphic gene expression across cell types, especially in the liver. Sex-dimorphic genes tended to be involved in processes related to lipid metabolism, and indeed, we observed clear differences in lipid storage in female vs. male turquoise killifish livers. Importantly, we use machine-learning to predict sex using single-cell gene expression in our atlas and identify potential transcriptional markers for molecular sex identity in this species. As proof-of-principle, we show that our atlas can be used to deconvolute existing liver bulk RNA-seq data in this species to obtain accurate estimates of cell type proportions across biological conditions. We believe that this single-cell atlas can be a resource to the community that could notably be leveraged to identify cell type-specific genes for cell type-specific expression in transgenic animals. Cold Spring Harbor Laboratory 2023-05-08 /pmc/articles/PMC10197525/ /pubmed/37214847 http://dx.doi.org/10.1101/2023.05.05.539616 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Teefy, Bryan B.
Lemus, Aaron J.J.
Adler, Ari
Xu, Alan
Bhala, Rajyk
Hsu, Katelyn
Benayoun, Bérénice A.
Widespread sex-dimorphism across single-cell transcriptomes of adult African turquoise killifish tissues
title Widespread sex-dimorphism across single-cell transcriptomes of adult African turquoise killifish tissues
title_full Widespread sex-dimorphism across single-cell transcriptomes of adult African turquoise killifish tissues
title_fullStr Widespread sex-dimorphism across single-cell transcriptomes of adult African turquoise killifish tissues
title_full_unstemmed Widespread sex-dimorphism across single-cell transcriptomes of adult African turquoise killifish tissues
title_short Widespread sex-dimorphism across single-cell transcriptomes of adult African turquoise killifish tissues
title_sort widespread sex-dimorphism across single-cell transcriptomes of adult african turquoise killifish tissues
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10197525/
https://www.ncbi.nlm.nih.gov/pubmed/37214847
http://dx.doi.org/10.1101/2023.05.05.539616
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