Transcriptomic analysis of dead end knockout testis reveals germ cell and gonadal somatic factors in Atlantic salmon

BACKGROUND: Sustainability challenges are currently hampering an increase in salmon production. Using sterile salmon can solve problems with precocious puberty and genetic introgression from farmed escapees to wild populations. Recently sterile salmon was produced by knocking out the germ cell-speci...

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Published in:BMC Genomics
Main Authors: Kleppe, Lene, Edvardsen, Rolf Brudvik, Furmanek, Tomasz, Andersson, Eva, Skaftnesmo, Kai Ove, Thyri Segafredo, Frida, Wargelius, Anna
Format: Text
Language:English
Published: BioMed Central 2020
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Online Access:http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6993523/
http://www.ncbi.nlm.nih.gov/pubmed/32000659
https://doi.org/10.1186/s12864-020-6513-4
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spelling ftpubmed:oai:pubmedcentral.nih.gov:6993523 2023-05-15T15:31:59+02:00 Transcriptomic analysis of dead end knockout testis reveals germ cell and gonadal somatic factors in Atlantic salmon Kleppe, Lene Edvardsen, Rolf Brudvik Furmanek, Tomasz Andersson, Eva Skaftnesmo, Kai Ove Thyri Segafredo, Frida Wargelius, Anna 2020-01-30 http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6993523/ http://www.ncbi.nlm.nih.gov/pubmed/32000659 https://doi.org/10.1186/s12864-020-6513-4 en eng BioMed Central http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6993523/ http://www.ncbi.nlm.nih.gov/pubmed/32000659 http://dx.doi.org/10.1186/s12864-020-6513-4 © The Author(s). 2020 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. CC0 PDM CC-BY Research Article Text 2020 ftpubmed https://doi.org/10.1186/s12864-020-6513-4 2020-02-09T01:35:50Z BACKGROUND: Sustainability challenges are currently hampering an increase in salmon production. Using sterile salmon can solve problems with precocious puberty and genetic introgression from farmed escapees to wild populations. Recently sterile salmon was produced by knocking out the germ cell-specific dead end (dnd). Several approaches may be applied to inhibit Dnd function, including gene knockout, knockdown or immunization. Since it is challenging to develop a successful treatment against a gene product already existing in the body, alternative targets are being explored. Germ cells are surrounded by, and dependent on, gonadal somatic cells. Targeting genes essential for the survival of gonadal somatic cells may be good alternative targets for sterility treatments. Our aim was to identify and characterize novel germ cell and gonadal somatic factors in Atlantic salmon. RESULTS: We have for the first time analysed RNA-sequencing data from germ cell-free (GCF)/dnd knockout and wild type (WT) salmon testis and searched for genes preferentially expressed in either germ cells or gonadal somatic cells. To exclude genes with extra-gonadal expression, our dataset was merged with available multi-tissue transcriptome data. We identified 389 gonad specific genes, of which 194 were preferentially expressed within germ cells, and 11 were confined to gonadal somatic cells. Interestingly, 5 of the 11 gonadal somatic transcripts represented genes encoding secreted TGF-β factors; gsdf, inha, nodal and two bmp6-like genes, all representative vaccine targets. Of these, gsdf and inha had the highest transcript levels. Expression of gsdf and inha was further confirmed to be gonad specific, and their spatial expression was restricted to granulosa and Sertoli cells of the ovary and testis, respectively. Finally, we show that inha expression increases with puberty in both ovary and testis tissue, while gsdf expression does not change or decreases during puberty in ovary and testis tissue, respectively. CONCLUSIONS: This study ... Text Atlantic salmon PubMed Central (PMC) BMC Genomics 21 1
institution Open Polar
collection PubMed Central (PMC)
op_collection_id ftpubmed
language English
topic Research Article
spellingShingle Research Article
Kleppe, Lene
Edvardsen, Rolf Brudvik
Furmanek, Tomasz
Andersson, Eva
Skaftnesmo, Kai Ove
Thyri Segafredo, Frida
Wargelius, Anna
Transcriptomic analysis of dead end knockout testis reveals germ cell and gonadal somatic factors in Atlantic salmon
topic_facet Research Article
description BACKGROUND: Sustainability challenges are currently hampering an increase in salmon production. Using sterile salmon can solve problems with precocious puberty and genetic introgression from farmed escapees to wild populations. Recently sterile salmon was produced by knocking out the germ cell-specific dead end (dnd). Several approaches may be applied to inhibit Dnd function, including gene knockout, knockdown or immunization. Since it is challenging to develop a successful treatment against a gene product already existing in the body, alternative targets are being explored. Germ cells are surrounded by, and dependent on, gonadal somatic cells. Targeting genes essential for the survival of gonadal somatic cells may be good alternative targets for sterility treatments. Our aim was to identify and characterize novel germ cell and gonadal somatic factors in Atlantic salmon. RESULTS: We have for the first time analysed RNA-sequencing data from germ cell-free (GCF)/dnd knockout and wild type (WT) salmon testis and searched for genes preferentially expressed in either germ cells or gonadal somatic cells. To exclude genes with extra-gonadal expression, our dataset was merged with available multi-tissue transcriptome data. We identified 389 gonad specific genes, of which 194 were preferentially expressed within germ cells, and 11 were confined to gonadal somatic cells. Interestingly, 5 of the 11 gonadal somatic transcripts represented genes encoding secreted TGF-β factors; gsdf, inha, nodal and two bmp6-like genes, all representative vaccine targets. Of these, gsdf and inha had the highest transcript levels. Expression of gsdf and inha was further confirmed to be gonad specific, and their spatial expression was restricted to granulosa and Sertoli cells of the ovary and testis, respectively. Finally, we show that inha expression increases with puberty in both ovary and testis tissue, while gsdf expression does not change or decreases during puberty in ovary and testis tissue, respectively. CONCLUSIONS: This study ...
format Text
author Kleppe, Lene
Edvardsen, Rolf Brudvik
Furmanek, Tomasz
Andersson, Eva
Skaftnesmo, Kai Ove
Thyri Segafredo, Frida
Wargelius, Anna
author_facet Kleppe, Lene
Edvardsen, Rolf Brudvik
Furmanek, Tomasz
Andersson, Eva
Skaftnesmo, Kai Ove
Thyri Segafredo, Frida
Wargelius, Anna
author_sort Kleppe, Lene
title Transcriptomic analysis of dead end knockout testis reveals germ cell and gonadal somatic factors in Atlantic salmon
title_short Transcriptomic analysis of dead end knockout testis reveals germ cell and gonadal somatic factors in Atlantic salmon
title_full Transcriptomic analysis of dead end knockout testis reveals germ cell and gonadal somatic factors in Atlantic salmon
title_fullStr Transcriptomic analysis of dead end knockout testis reveals germ cell and gonadal somatic factors in Atlantic salmon
title_full_unstemmed Transcriptomic analysis of dead end knockout testis reveals germ cell and gonadal somatic factors in Atlantic salmon
title_sort transcriptomic analysis of dead end knockout testis reveals germ cell and gonadal somatic factors in atlantic salmon
publisher BioMed Central
publishDate 2020
url http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6993523/
http://www.ncbi.nlm.nih.gov/pubmed/32000659
https://doi.org/10.1186/s12864-020-6513-4
genre Atlantic salmon
genre_facet Atlantic salmon
op_relation http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6993523/
http://www.ncbi.nlm.nih.gov/pubmed/32000659
http://dx.doi.org/10.1186/s12864-020-6513-4
op_rights © The Author(s). 2020
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
op_rightsnorm CC0
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CC-BY
op_doi https://doi.org/10.1186/s12864-020-6513-4
container_title BMC Genomics
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