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Defining a role for lung function associated gene GSTCD in cell homeostasis

Genome wide association (GWA) studies have reproducibly identified signals on chromosome 4q24 associated with lung function and COPD. GSTCD (Glutathione S-transferase C-terminal domain containing) represents a candidate causal gene in this locus, however little is currently known about the function...

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Autores principales: Henry, Amanda P., Probert, Kelly, Stewart, Ceri E., Thakker, Dhruma, Bhaker, Sangita, Azimi, Sheyda, Hall, Ian P., Sayers, Ian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6676530/
https://www.ncbi.nlm.nih.gov/pubmed/31370853
http://dx.doi.org/10.1186/s12931-019-1146-3
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author Henry, Amanda P.
Probert, Kelly
Stewart, Ceri E.
Thakker, Dhruma
Bhaker, Sangita
Azimi, Sheyda
Hall, Ian P.
Sayers, Ian
author_facet Henry, Amanda P.
Probert, Kelly
Stewart, Ceri E.
Thakker, Dhruma
Bhaker, Sangita
Azimi, Sheyda
Hall, Ian P.
Sayers, Ian
author_sort Henry, Amanda P.
collection PubMed
description Genome wide association (GWA) studies have reproducibly identified signals on chromosome 4q24 associated with lung function and COPD. GSTCD (Glutathione S-transferase C-terminal domain containing) represents a candidate causal gene in this locus, however little is currently known about the function of this protein. We set out to further our understanding of the role of GSTCD in cell functions and homeostasis using multiple molecular and cellular approaches in airway relevant cells. Recombinant expression of human GSTCD in conjunction with a GST activity assay did not identify any enzymatic activity for two GSTCD isoforms questioning the assignment of this protein to this family of enzymes. Protein structure analyses identified a potential methyltransferase domain contained within GSTCD, with these enzymes linked to cell viability and apoptosis. Targeted knockdown (siRNA) of GSTCD in bronchial epithelial cells identified a role for GSTCD in cell viability as proliferation rates were not altered. To provide greater insight we completed transcriptomic analyses on cells with GSTCD expression knocked down and identified several differentially expressed genes including those implicated in airway biology; fibrosis e.g. TGFBR1 and inflammation e.g. IL6R. Pathway based transcriptomic analyses identified an over-representation of genes related to adipogenesis which may suggest additional functions for GSTCD. These findings identify potential additional functions for GSTCD in the context of airway biology beyond the hypothesised GST activity and warrant further investigation.
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spelling pubmed-66765302019-08-06 Defining a role for lung function associated gene GSTCD in cell homeostasis Henry, Amanda P. Probert, Kelly Stewart, Ceri E. Thakker, Dhruma Bhaker, Sangita Azimi, Sheyda Hall, Ian P. Sayers, Ian Respir Res Research Genome wide association (GWA) studies have reproducibly identified signals on chromosome 4q24 associated with lung function and COPD. GSTCD (Glutathione S-transferase C-terminal domain containing) represents a candidate causal gene in this locus, however little is currently known about the function of this protein. We set out to further our understanding of the role of GSTCD in cell functions and homeostasis using multiple molecular and cellular approaches in airway relevant cells. Recombinant expression of human GSTCD in conjunction with a GST activity assay did not identify any enzymatic activity for two GSTCD isoforms questioning the assignment of this protein to this family of enzymes. Protein structure analyses identified a potential methyltransferase domain contained within GSTCD, with these enzymes linked to cell viability and apoptosis. Targeted knockdown (siRNA) of GSTCD in bronchial epithelial cells identified a role for GSTCD in cell viability as proliferation rates were not altered. To provide greater insight we completed transcriptomic analyses on cells with GSTCD expression knocked down and identified several differentially expressed genes including those implicated in airway biology; fibrosis e.g. TGFBR1 and inflammation e.g. IL6R. Pathway based transcriptomic analyses identified an over-representation of genes related to adipogenesis which may suggest additional functions for GSTCD. These findings identify potential additional functions for GSTCD in the context of airway biology beyond the hypothesised GST activity and warrant further investigation. BioMed Central 2019-08-01 2019 /pmc/articles/PMC6676530/ /pubmed/31370853 http://dx.doi.org/10.1186/s12931-019-1146-3 Text en © The Author(s). 2019 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.
spellingShingle Research
Henry, Amanda P.
Probert, Kelly
Stewart, Ceri E.
Thakker, Dhruma
Bhaker, Sangita
Azimi, Sheyda
Hall, Ian P.
Sayers, Ian
Defining a role for lung function associated gene GSTCD in cell homeostasis
title Defining a role for lung function associated gene GSTCD in cell homeostasis
title_full Defining a role for lung function associated gene GSTCD in cell homeostasis
title_fullStr Defining a role for lung function associated gene GSTCD in cell homeostasis
title_full_unstemmed Defining a role for lung function associated gene GSTCD in cell homeostasis
title_short Defining a role for lung function associated gene GSTCD in cell homeostasis
title_sort defining a role for lung function associated gene gstcd in cell homeostasis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6676530/
https://www.ncbi.nlm.nih.gov/pubmed/31370853
http://dx.doi.org/10.1186/s12931-019-1146-3
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