Ferredoxin 1 is essential for embryonic development and lipid homeostasis.

cancer biology mouse

Journal

eLife
ISSN: 2050-084X
Titre abrégé: Elife
Pays: England
ID NLM: 101579614

Informations de publication

Date de publication:
22 Jan 2024
Historique:
received: 06 08 2023
accepted: 19 01 2024
medline: 22 1 2024
pubmed: 22 1 2024
entrez: 22 1 2024
Statut: aheadofprint

Résumé

Mammalian ferredoxin 1 and 2 (FDX1/2) belong to an evolutionary conserved family of iron-sulfur cluster containing proteins and act as electron shutters between ferredoxin reductase (FDXR) and numerous proteins involved in critical biological pathways. FDX1 is involved in biogenesis of steroids and bile acids, Vitamin A/D metabolism, and lipoylation of tricarboxylic acid (TCA) cycle enzymes. FDX1 has been extensively characterized biochemically but its role in physiology and lipid metabolism has not been explored. In this study, we generated

Identifiants

pubmed: 38251655
doi: 10.7554/eLife.91656
pii: 91656
doi:
pii:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIH HHS
ID : CA224433
Pays : United States

Informations de copyright

© 2024, Mohibi et al.

Déclaration de conflit d'intérêts

SM, YZ, VP, MC, JZ, XC The authors declare that no competing interests exist.

Auteurs

Shakur Mohibi (S)

Comparative Oncology Laboratory, University of California, Davis, Davis, United States.

Yanhong Zhang (Y)

Comparative Oncology Laboratory, University of California, Davis, Davis, United States.

Vivian Perng (V)

Comparative Oncology Laboratory, University of California, Davis, Davis, United States.

Mingyi Chen (M)

Department of Pathology, The University of Texas Southwestern Medical Center, Dallas, United States.

Jin Zhang (J)

Center for Comparative Oncology, University of California, Davis, Davis, United States.

Xinbin Chen (X)

Comparative Oncology Laboratory, University of California, Davis, Davis, United States.

Classifications MeSH