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Energy balance-dependent regulation of ovine glucose 6-phosphate dehydrogenase protein isoform expression

G6PDH is the rate-limiting enzyme of the pentose phosphate pathway and one of the principal source of NADPH, a major cellular reductant. Importantly, in ruminant's metabolism the aforementioned NADPH provided, is utilized for de novo fatty acid synthesis. Previous work of cloning the ovine (Ovi...

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Autores principales: Triantaphyllopoulos, Kostas A, Laliotis, George P, Bizelis, Iosif A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3917929/
https://www.ncbi.nlm.nih.gov/pubmed/24575366
http://dx.doi.org/10.4161/adip.26437
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author Triantaphyllopoulos, Kostas A
Laliotis, George P
Bizelis, Iosif A
author_facet Triantaphyllopoulos, Kostas A
Laliotis, George P
Bizelis, Iosif A
author_sort Triantaphyllopoulos, Kostas A
collection PubMed
description G6PDH is the rate-limiting enzyme of the pentose phosphate pathway and one of the principal source of NADPH, a major cellular reductant. Importantly, in ruminant's metabolism the aforementioned NADPH provided, is utilized for de novo fatty acid synthesis. Previous work of cloning the ovine (Ovis aries) og6pdh gene has revealed the presence of two cDNA transcripts (og6pda and og6pdb), og6pdb being a product of alternative splicing not similar to any other previously reported.(1) In the current study the effect of energy balance in the ovine G6PDH protein expression was investigated, shedding light on the biochemical features and potential physiological role of the oG6PDB isoform. Changes in energy balance leads to protein expression changes in both transcripts, to the opposite direction and not in a proportional way. Negative energy balance was not in favor of the presence of any particular isoform, while both protein expression levels were not significantly different (P > 0.05). In contrast, at the transition point from negative to positive and on the positive energy balance, there is a significant increase of oG6PDA compared with oG6PDB protein expression (P < 0.001). Both oG6PDH protein isoforms changed significantly toward the positive energy balance. oG6PDA is escalating, while oG6PDB is falling, under the same stimulus (positive energy balance alteration). This change is also positively associated with increasing levels in enzyme activity, 4 weeks post-weaning in ewes’ adipose tissue. Furthermore, regression analysis clearly demonstrated the linear correlation of both proteins in response to the WPW, while energy balance, enzyme activity, and oG6PDA relative protein expression follow the same escalating trend; in contrast, oG6PDB relative protein expression falls in time, similar to both transcripts accumulation pattern, as reported previously.(2)
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spelling pubmed-39179292014-02-26 Energy balance-dependent regulation of ovine glucose 6-phosphate dehydrogenase protein isoform expression Triantaphyllopoulos, Kostas A Laliotis, George P Bizelis, Iosif A Adipocyte Research Paper G6PDH is the rate-limiting enzyme of the pentose phosphate pathway and one of the principal source of NADPH, a major cellular reductant. Importantly, in ruminant's metabolism the aforementioned NADPH provided, is utilized for de novo fatty acid synthesis. Previous work of cloning the ovine (Ovis aries) og6pdh gene has revealed the presence of two cDNA transcripts (og6pda and og6pdb), og6pdb being a product of alternative splicing not similar to any other previously reported.(1) In the current study the effect of energy balance in the ovine G6PDH protein expression was investigated, shedding light on the biochemical features and potential physiological role of the oG6PDB isoform. Changes in energy balance leads to protein expression changes in both transcripts, to the opposite direction and not in a proportional way. Negative energy balance was not in favor of the presence of any particular isoform, while both protein expression levels were not significantly different (P > 0.05). In contrast, at the transition point from negative to positive and on the positive energy balance, there is a significant increase of oG6PDA compared with oG6PDB protein expression (P < 0.001). Both oG6PDH protein isoforms changed significantly toward the positive energy balance. oG6PDA is escalating, while oG6PDB is falling, under the same stimulus (positive energy balance alteration). This change is also positively associated with increasing levels in enzyme activity, 4 weeks post-weaning in ewes’ adipose tissue. Furthermore, regression analysis clearly demonstrated the linear correlation of both proteins in response to the WPW, while energy balance, enzyme activity, and oG6PDA relative protein expression follow the same escalating trend; in contrast, oG6PDB relative protein expression falls in time, similar to both transcripts accumulation pattern, as reported previously.(2) Landes Bioscience 2014-01-01 2013-10-11 /pmc/articles/PMC3917929/ /pubmed/24575366 http://dx.doi.org/10.4161/adip.26437 Text en Copyright © 2014 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Research Paper
Triantaphyllopoulos, Kostas A
Laliotis, George P
Bizelis, Iosif A
Energy balance-dependent regulation of ovine glucose 6-phosphate dehydrogenase protein isoform expression
title Energy balance-dependent regulation of ovine glucose 6-phosphate dehydrogenase protein isoform expression
title_full Energy balance-dependent regulation of ovine glucose 6-phosphate dehydrogenase protein isoform expression
title_fullStr Energy balance-dependent regulation of ovine glucose 6-phosphate dehydrogenase protein isoform expression
title_full_unstemmed Energy balance-dependent regulation of ovine glucose 6-phosphate dehydrogenase protein isoform expression
title_short Energy balance-dependent regulation of ovine glucose 6-phosphate dehydrogenase protein isoform expression
title_sort energy balance-dependent regulation of ovine glucose 6-phosphate dehydrogenase protein isoform expression
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3917929/
https://www.ncbi.nlm.nih.gov/pubmed/24575366
http://dx.doi.org/10.4161/adip.26437
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