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Comparative transcriptomics suggest unique molecular adaptations within tardigrade lineages

BACKGROUND: Tardigrades are renowned for their ability to enter cryptobiosis (latent life) and endure extreme stress, including desiccation and freezing. Increased focus is on revealing molecular mechanisms underlying this tolerance. Here, we provide the first transcriptomes from the heterotardigrad...

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Autores principales: Kamilari, Maria, Jørgensen, Aslak, Schiøtt, Morten, Møbjerg, Nadja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6652013/
https://www.ncbi.nlm.nih.gov/pubmed/31340759
http://dx.doi.org/10.1186/s12864-019-5912-x
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author Kamilari, Maria
Jørgensen, Aslak
Schiøtt, Morten
Møbjerg, Nadja
author_facet Kamilari, Maria
Jørgensen, Aslak
Schiøtt, Morten
Møbjerg, Nadja
author_sort Kamilari, Maria
collection PubMed
description BACKGROUND: Tardigrades are renowned for their ability to enter cryptobiosis (latent life) and endure extreme stress, including desiccation and freezing. Increased focus is on revealing molecular mechanisms underlying this tolerance. Here, we provide the first transcriptomes from the heterotardigrade Echiniscoides cf. sigismundi and the eutardigrade Richtersius cf. coronifer, and compare these with data from other tardigrades and six eukaryote models. Investigating 107 genes/gene families, our study provides a thorough analysis of tardigrade gene content with focus on stress tolerance. RESULTS: E. cf. sigismundi, a strong cryptobiont, apparently lacks expression of a number of stress related genes. Most conspicuous is the lack of transcripts from genes involved in classical Non-Homologous End Joining. Our analyses suggest that post-cryptobiotic survival in tardigrades could rely on high fidelity transcription-coupled DNA repair. Tardigrades seem to lack many peroxins, but they all have a comprehensive number of genes encoding proteins involved in antioxidant defense. The “tardigrade unique proteins” (CAHS, SAHS, MAHS, RvLEAM), seem to be missing in the heterotardigrade lineage, revealing that cryptobiosis in general cannot be attributed solely to these proteins. Our investigation further reveals a unique and highly expressed cold shock domain. We hypothesize that the cold shock protein acts as a RNA-chaperone involved in regulation of translation following freezing. CONCLUSIONS: Our results show common gene family contractions and expansions within stress related gene pathways in tardigrades, but also indicate that evolutionary lineages have a high degree of divergence. Different taxa and lineages may exhibit unique physiological adaptations towards stress conditions involving possible unknown functional homologues and/or novel physiological and biochemical mechanisms. To further substantiate the current results genome assemblies coupled with transcriptome data and experimental investigations are needed from tardigrades belonging to different evolutionary lineages. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-019-5912-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-66520132019-07-31 Comparative transcriptomics suggest unique molecular adaptations within tardigrade lineages Kamilari, Maria Jørgensen, Aslak Schiøtt, Morten Møbjerg, Nadja BMC Genomics Research Article BACKGROUND: Tardigrades are renowned for their ability to enter cryptobiosis (latent life) and endure extreme stress, including desiccation and freezing. Increased focus is on revealing molecular mechanisms underlying this tolerance. Here, we provide the first transcriptomes from the heterotardigrade Echiniscoides cf. sigismundi and the eutardigrade Richtersius cf. coronifer, and compare these with data from other tardigrades and six eukaryote models. Investigating 107 genes/gene families, our study provides a thorough analysis of tardigrade gene content with focus on stress tolerance. RESULTS: E. cf. sigismundi, a strong cryptobiont, apparently lacks expression of a number of stress related genes. Most conspicuous is the lack of transcripts from genes involved in classical Non-Homologous End Joining. Our analyses suggest that post-cryptobiotic survival in tardigrades could rely on high fidelity transcription-coupled DNA repair. Tardigrades seem to lack many peroxins, but they all have a comprehensive number of genes encoding proteins involved in antioxidant defense. The “tardigrade unique proteins” (CAHS, SAHS, MAHS, RvLEAM), seem to be missing in the heterotardigrade lineage, revealing that cryptobiosis in general cannot be attributed solely to these proteins. Our investigation further reveals a unique and highly expressed cold shock domain. We hypothesize that the cold shock protein acts as a RNA-chaperone involved in regulation of translation following freezing. CONCLUSIONS: Our results show common gene family contractions and expansions within stress related gene pathways in tardigrades, but also indicate that evolutionary lineages have a high degree of divergence. Different taxa and lineages may exhibit unique physiological adaptations towards stress conditions involving possible unknown functional homologues and/or novel physiological and biochemical mechanisms. To further substantiate the current results genome assemblies coupled with transcriptome data and experimental investigations are needed from tardigrades belonging to different evolutionary lineages. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-019-5912-x) contains supplementary material, which is available to authorized users. BioMed Central 2019-07-24 /pmc/articles/PMC6652013/ /pubmed/31340759 http://dx.doi.org/10.1186/s12864-019-5912-x Text en © The Author(s). 2019 Open Access This 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.
spellingShingle Research Article
Kamilari, Maria
Jørgensen, Aslak
Schiøtt, Morten
Møbjerg, Nadja
Comparative transcriptomics suggest unique molecular adaptations within tardigrade lineages
title Comparative transcriptomics suggest unique molecular adaptations within tardigrade lineages
title_full Comparative transcriptomics suggest unique molecular adaptations within tardigrade lineages
title_fullStr Comparative transcriptomics suggest unique molecular adaptations within tardigrade lineages
title_full_unstemmed Comparative transcriptomics suggest unique molecular adaptations within tardigrade lineages
title_short Comparative transcriptomics suggest unique molecular adaptations within tardigrade lineages
title_sort comparative transcriptomics suggest unique molecular adaptations within tardigrade lineages
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6652013/
https://www.ncbi.nlm.nih.gov/pubmed/31340759
http://dx.doi.org/10.1186/s12864-019-5912-x
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