Ferredoxin 1b (Fdx1b) is the essential mitochondrial redox partner for cortisol biosynthesis in zebrafish

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@article{6449f9859184424f90f6203cb210759e,
title = "Ferredoxin 1b (Fdx1b) is the essential mitochondrial redox partner for cortisol biosynthesis in zebrafish",
abstract = "Mitochondrial cytochrome P450 (CYP) enzymes rely on electron transfer from the redox partner ferredoxin (FDX1) for catalytic activity. Key steps in steroidogenesis require mitochondrial CYP enzymes and FDX1. Over 30 ferredoxin mutations have been explored in vitro, however, no spontaneously occurring mutations have been identified in humans leaving the impact of FDX1 on steroidogenesis in the whole organism largely unknown. Zebrafish are an important model to study human steroidogenesis as they have similar steroid products and endocrine tissues. This study aimed to characterise the influence of ferredoxin on steroidogenic capacity in vivo by using zebrafish. Zebrafish have duplicate ferredoxin paralogs: fdx1 and fdx1b. While fdx1 was observed throughout development and in most tissues, fdx1b was expressed after development of the zebrafish interrenal gland (counterpart to the mammalian adrenal gland). Additionally, fdx1b was restricted to adult steroidogenic tissues, such as the interrenal, gonads, and brain; suggesting fdx1b was interacting with steroidogenic CYP enzymes. By using Transcription Activator-Like Effector Nucleases (TALENs) we generated fdx1b mutant zebrafish lines. Larvae with genetic disruption of fdx1b were morphologically inconspicuous. However, steroid hormone analysis by liquid chromatography tandem-mass spectrometry revealed fdx1b mutants failed to synthesise glucocorticoids. Additionally, these mutants had an up-regulation of the hypothalamus-pituitary-interrenal axis, and showed altered dark-light adaptation suggesting impaired cortisol signalling. Anti-sense morpholino knockdown confirmed Fdx1b is required for de novo cortisol biosynthesis. In summary, by using zebrafish we generated a ferredoxin knockout model system, which demonstrates for the first time the impact of mitochondrial redox regulation on glucocorticoid biosynthesis in vivo.",
author = "Aliesha Griffin and Silvia Parajes and Meltem Weger and Andreas Zaucker and Taylor, {Angela E} and O'Neil, {Donna M} and Ferenc M{\"u}ller and Nils Krone",
year = "2016",
month = mar,
doi = "10.1210/en.2015-1480",
language = "English",
volume = "157",
journal = "Endocrinology",
issn = "0013-7227",
publisher = "Endocrine Society",
number = "3",

}

RIS

TY - JOUR

T1 - Ferredoxin 1b (Fdx1b) is the essential mitochondrial redox partner for cortisol biosynthesis in zebrafish

AU - Griffin, Aliesha

AU - Parajes, Silvia

AU - Weger, Meltem

AU - Zaucker, Andreas

AU - Taylor, Angela E

AU - O'Neil, Donna M

AU - Müller, Ferenc

AU - Krone, Nils

PY - 2016/3

Y1 - 2016/3

N2 - Mitochondrial cytochrome P450 (CYP) enzymes rely on electron transfer from the redox partner ferredoxin (FDX1) for catalytic activity. Key steps in steroidogenesis require mitochondrial CYP enzymes and FDX1. Over 30 ferredoxin mutations have been explored in vitro, however, no spontaneously occurring mutations have been identified in humans leaving the impact of FDX1 on steroidogenesis in the whole organism largely unknown. Zebrafish are an important model to study human steroidogenesis as they have similar steroid products and endocrine tissues. This study aimed to characterise the influence of ferredoxin on steroidogenic capacity in vivo by using zebrafish. Zebrafish have duplicate ferredoxin paralogs: fdx1 and fdx1b. While fdx1 was observed throughout development and in most tissues, fdx1b was expressed after development of the zebrafish interrenal gland (counterpart to the mammalian adrenal gland). Additionally, fdx1b was restricted to adult steroidogenic tissues, such as the interrenal, gonads, and brain; suggesting fdx1b was interacting with steroidogenic CYP enzymes. By using Transcription Activator-Like Effector Nucleases (TALENs) we generated fdx1b mutant zebrafish lines. Larvae with genetic disruption of fdx1b were morphologically inconspicuous. However, steroid hormone analysis by liquid chromatography tandem-mass spectrometry revealed fdx1b mutants failed to synthesise glucocorticoids. Additionally, these mutants had an up-regulation of the hypothalamus-pituitary-interrenal axis, and showed altered dark-light adaptation suggesting impaired cortisol signalling. Anti-sense morpholino knockdown confirmed Fdx1b is required for de novo cortisol biosynthesis. In summary, by using zebrafish we generated a ferredoxin knockout model system, which demonstrates for the first time the impact of mitochondrial redox regulation on glucocorticoid biosynthesis in vivo.

AB - Mitochondrial cytochrome P450 (CYP) enzymes rely on electron transfer from the redox partner ferredoxin (FDX1) for catalytic activity. Key steps in steroidogenesis require mitochondrial CYP enzymes and FDX1. Over 30 ferredoxin mutations have been explored in vitro, however, no spontaneously occurring mutations have been identified in humans leaving the impact of FDX1 on steroidogenesis in the whole organism largely unknown. Zebrafish are an important model to study human steroidogenesis as they have similar steroid products and endocrine tissues. This study aimed to characterise the influence of ferredoxin on steroidogenic capacity in vivo by using zebrafish. Zebrafish have duplicate ferredoxin paralogs: fdx1 and fdx1b. While fdx1 was observed throughout development and in most tissues, fdx1b was expressed after development of the zebrafish interrenal gland (counterpart to the mammalian adrenal gland). Additionally, fdx1b was restricted to adult steroidogenic tissues, such as the interrenal, gonads, and brain; suggesting fdx1b was interacting with steroidogenic CYP enzymes. By using Transcription Activator-Like Effector Nucleases (TALENs) we generated fdx1b mutant zebrafish lines. Larvae with genetic disruption of fdx1b were morphologically inconspicuous. However, steroid hormone analysis by liquid chromatography tandem-mass spectrometry revealed fdx1b mutants failed to synthesise glucocorticoids. Additionally, these mutants had an up-regulation of the hypothalamus-pituitary-interrenal axis, and showed altered dark-light adaptation suggesting impaired cortisol signalling. Anti-sense morpholino knockdown confirmed Fdx1b is required for de novo cortisol biosynthesis. In summary, by using zebrafish we generated a ferredoxin knockout model system, which demonstrates for the first time the impact of mitochondrial redox regulation on glucocorticoid biosynthesis in vivo.

U2 - 10.1210/en.2015-1480

DO - 10.1210/en.2015-1480

M3 - Article

C2 - 26650568

VL - 157

JO - Endocrinology

JF - Endocrinology

SN - 0013-7227

IS - 3

ER -