A Caenorhabditis elegans ortholog of human selenium-binding protein 1 is a pro-aging factor protecting against selenite toxicity

Human selenium-binding protein 1 (SELENBP1) was originally identified as a protein binding selenium, most likely as selenite. SELENBP1 is associated with cellular redox and thiol homeostasis in several respects, including its established role as a methanethiol oxidase that is involved in degradation...

Full description

Bibliographic Details
Main Authors: Karl Köhnlein, Nadine Urban, David Guerrero-Gómez, Holger Steinbrenner, Pavel Urbánek, Josephine Priebs, Philipp Koch, Christoph Kaether, Antonio Miranda-Vizuete, Lars-Oliver Klotz
Format: Article
Language:English
Published: Elsevier 2020-01-01
Series:Redox Biology
Online Access:http://www.sciencedirect.com/science/article/pii/S2213231719308419
id doaj-81369527dd3f45ca84991cf3cfbad8a7
record_format Article
spelling doaj-81369527dd3f45ca84991cf3cfbad8a72020-11-24T21:57:28ZengElsevierRedox Biology2213-23172020-01-0128A Caenorhabditis elegans ortholog of human selenium-binding protein 1 is a pro-aging factor protecting against selenite toxicityKarl Köhnlein0Nadine Urban1David Guerrero-Gómez2Holger Steinbrenner3Pavel Urbánek4Josephine Priebs5Philipp Koch6Christoph Kaether7Antonio Miranda-Vizuete8Lars-Oliver Klotz9Institute of Nutritional Sciences, Nutrigenomics Section, Friedrich-Schiller-Universität Jena, Jena, Germany; Leibniz Institute on Aging - Fritz Lipmann Institute, Jena, GermanyInstitute of Nutritional Sciences, Nutrigenomics Section, Friedrich-Schiller-Universität Jena, Jena, GermanyInstituto de Biomedicina de Sevilla (IBIS), Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla, Sevilla, SpainInstitute of Nutritional Sciences, Nutrigenomics Section, Friedrich-Schiller-Universität Jena, Jena, GermanyInstitute of Nutritional Sciences, Nutrigenomics Section, Friedrich-Schiller-Universität Jena, Jena, GermanyInstitute of Nutritional Sciences, Nutrigenomics Section, Friedrich-Schiller-Universität Jena, Jena, GermanyLeibniz Institute on Aging - Fritz Lipmann Institute, Jena, GermanyLeibniz Institute on Aging - Fritz Lipmann Institute, Jena, GermanyInstituto de Biomedicina de Sevilla (IBIS), Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla, Sevilla, SpainInstitute of Nutritional Sciences, Nutrigenomics Section, Friedrich-Schiller-Universität Jena, Jena, Germany; Corresponding author. Institute of Nutritional Sciences, Nutrigenomics Section, Friedrich Schiller University Jena, Dornburger Strasse 29, Jena, D-07743, Germany.Human selenium-binding protein 1 (SELENBP1) was originally identified as a protein binding selenium, most likely as selenite. SELENBP1 is associated with cellular redox and thiol homeostasis in several respects, including its established role as a methanethiol oxidase that is involved in degradation of methanethiol, a methionine catabolite, generating hydrogen sulfide (H2S) and hydrogen peroxide (H2O2). As both H2S and reactive oxygen species (such as H2O2) are major regulators of Caenorhabditis elegans lifespan and stress resistance, we hypothesized that a SELENBP1 ortholog in C. elegans would likely be involved in regulating these aspects.Here we characterize Y37A1B.5, a putative selenium-binding protein 1 ortholog in C. elegans with 52% primary structure identity to human SELENBP1. While conferring resistance to toxic concentrations of selenite, Y37A1B.5 also attenuates resistance to oxidative stress and lowers C. elegans lifespan: knockdown of Y37A1B.5 using RNA interference resulted in an approx. 10% increase of C. elegans lifespan and an enhanced resistance against the redox cycler paraquat, as well as enhanced motility. Analyses of transgenic reporter strains suggest hypodermal expression and cytoplasmic localization of Y37A1B.5, whose expression decreases with worm age. We identify the transcriptional coregulator MDT-15 and transcription factor EGL-27 as regulators of Y37A1B.5 levels and show that the lifespan extending effect elicited by downregulation of Y37A1B.5 is independent of known MDT-15 interacting factors, such as DAF-16 and NHR-49. In summary, Y37A1B.5 is an ortholog of SELENBP1 that shortens C. elegans lifespan and lowers resistance against oxidative stress, while allowing for a better survival under toxic selenite concentrations. Keywords: Selenium-binding protein, Stress signaling, Caenorhabditis elegans, Lifespanhttp://www.sciencedirect.com/science/article/pii/S2213231719308419
collection DOAJ
language English
format Article
sources DOAJ
author Karl Köhnlein
Nadine Urban
David Guerrero-Gómez
Holger Steinbrenner
Pavel Urbánek
Josephine Priebs
Philipp Koch
Christoph Kaether
Antonio Miranda-Vizuete
Lars-Oliver Klotz
spellingShingle Karl Köhnlein
Nadine Urban
David Guerrero-Gómez
Holger Steinbrenner
Pavel Urbánek
Josephine Priebs
Philipp Koch
Christoph Kaether
Antonio Miranda-Vizuete
Lars-Oliver Klotz
A Caenorhabditis elegans ortholog of human selenium-binding protein 1 is a pro-aging factor protecting against selenite toxicity
Redox Biology
author_facet Karl Köhnlein
Nadine Urban
David Guerrero-Gómez
Holger Steinbrenner
Pavel Urbánek
Josephine Priebs
Philipp Koch
Christoph Kaether
Antonio Miranda-Vizuete
Lars-Oliver Klotz
author_sort Karl Köhnlein
title A Caenorhabditis elegans ortholog of human selenium-binding protein 1 is a pro-aging factor protecting against selenite toxicity
title_short A Caenorhabditis elegans ortholog of human selenium-binding protein 1 is a pro-aging factor protecting against selenite toxicity
title_full A Caenorhabditis elegans ortholog of human selenium-binding protein 1 is a pro-aging factor protecting against selenite toxicity
title_fullStr A Caenorhabditis elegans ortholog of human selenium-binding protein 1 is a pro-aging factor protecting against selenite toxicity
title_full_unstemmed A Caenorhabditis elegans ortholog of human selenium-binding protein 1 is a pro-aging factor protecting against selenite toxicity
title_sort caenorhabditis elegans ortholog of human selenium-binding protein 1 is a pro-aging factor protecting against selenite toxicity
publisher Elsevier
series Redox Biology
issn 2213-2317
publishDate 2020-01-01
description Human selenium-binding protein 1 (SELENBP1) was originally identified as a protein binding selenium, most likely as selenite. SELENBP1 is associated with cellular redox and thiol homeostasis in several respects, including its established role as a methanethiol oxidase that is involved in degradation of methanethiol, a methionine catabolite, generating hydrogen sulfide (H2S) and hydrogen peroxide (H2O2). As both H2S and reactive oxygen species (such as H2O2) are major regulators of Caenorhabditis elegans lifespan and stress resistance, we hypothesized that a SELENBP1 ortholog in C. elegans would likely be involved in regulating these aspects.Here we characterize Y37A1B.5, a putative selenium-binding protein 1 ortholog in C. elegans with 52% primary structure identity to human SELENBP1. While conferring resistance to toxic concentrations of selenite, Y37A1B.5 also attenuates resistance to oxidative stress and lowers C. elegans lifespan: knockdown of Y37A1B.5 using RNA interference resulted in an approx. 10% increase of C. elegans lifespan and an enhanced resistance against the redox cycler paraquat, as well as enhanced motility. Analyses of transgenic reporter strains suggest hypodermal expression and cytoplasmic localization of Y37A1B.5, whose expression decreases with worm age. We identify the transcriptional coregulator MDT-15 and transcription factor EGL-27 as regulators of Y37A1B.5 levels and show that the lifespan extending effect elicited by downregulation of Y37A1B.5 is independent of known MDT-15 interacting factors, such as DAF-16 and NHR-49. In summary, Y37A1B.5 is an ortholog of SELENBP1 that shortens C. elegans lifespan and lowers resistance against oxidative stress, while allowing for a better survival under toxic selenite concentrations. Keywords: Selenium-binding protein, Stress signaling, Caenorhabditis elegans, Lifespan
url http://www.sciencedirect.com/science/article/pii/S2213231719308419
work_keys_str_mv AT karlkohnlein acaenorhabditiselegansorthologofhumanseleniumbindingprotein1isaproagingfactorprotectingagainstselenitetoxicity
AT nadineurban acaenorhabditiselegansorthologofhumanseleniumbindingprotein1isaproagingfactorprotectingagainstselenitetoxicity
AT davidguerrerogomez acaenorhabditiselegansorthologofhumanseleniumbindingprotein1isaproagingfactorprotectingagainstselenitetoxicity
AT holgersteinbrenner acaenorhabditiselegansorthologofhumanseleniumbindingprotein1isaproagingfactorprotectingagainstselenitetoxicity
AT pavelurbanek acaenorhabditiselegansorthologofhumanseleniumbindingprotein1isaproagingfactorprotectingagainstselenitetoxicity
AT josephinepriebs acaenorhabditiselegansorthologofhumanseleniumbindingprotein1isaproagingfactorprotectingagainstselenitetoxicity
AT philippkoch acaenorhabditiselegansorthologofhumanseleniumbindingprotein1isaproagingfactorprotectingagainstselenitetoxicity
AT christophkaether acaenorhabditiselegansorthologofhumanseleniumbindingprotein1isaproagingfactorprotectingagainstselenitetoxicity
AT antoniomirandavizuete acaenorhabditiselegansorthologofhumanseleniumbindingprotein1isaproagingfactorprotectingagainstselenitetoxicity
AT larsoliverklotz acaenorhabditiselegansorthologofhumanseleniumbindingprotein1isaproagingfactorprotectingagainstselenitetoxicity
AT karlkohnlein caenorhabditiselegansorthologofhumanseleniumbindingprotein1isaproagingfactorprotectingagainstselenitetoxicity
AT nadineurban caenorhabditiselegansorthologofhumanseleniumbindingprotein1isaproagingfactorprotectingagainstselenitetoxicity
AT davidguerrerogomez caenorhabditiselegansorthologofhumanseleniumbindingprotein1isaproagingfactorprotectingagainstselenitetoxicity
AT holgersteinbrenner caenorhabditiselegansorthologofhumanseleniumbindingprotein1isaproagingfactorprotectingagainstselenitetoxicity
AT pavelurbanek caenorhabditiselegansorthologofhumanseleniumbindingprotein1isaproagingfactorprotectingagainstselenitetoxicity
AT josephinepriebs caenorhabditiselegansorthologofhumanseleniumbindingprotein1isaproagingfactorprotectingagainstselenitetoxicity
AT philippkoch caenorhabditiselegansorthologofhumanseleniumbindingprotein1isaproagingfactorprotectingagainstselenitetoxicity
AT christophkaether caenorhabditiselegansorthologofhumanseleniumbindingprotein1isaproagingfactorprotectingagainstselenitetoxicity
AT antoniomirandavizuete caenorhabditiselegansorthologofhumanseleniumbindingprotein1isaproagingfactorprotectingagainstselenitetoxicity
AT larsoliverklotz caenorhabditiselegansorthologofhumanseleniumbindingprotein1isaproagingfactorprotectingagainstselenitetoxicity
_version_ 1725855361540292608