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A dominant negative ADIPOQ mutation in a diabetic family with renal disease, hypoadiponectinemia, and hyperceramidemia.

Authors :
Simeone CA
Wilkerson JL
Poss AM
Banks JA
Varre JV
Guevara JL
Hernandez EJ
Gorsi B
Atkinson DL
Turapov T
Frodsham SG
Morales JCF
O'Neil K
Moore B
Yandell M
Summers SA
Krolewski AS
Holland WL
Pezzolesi MG
Source :
NPJ genomic medicine [NPJ Genom Med] 2022 Jul 22; Vol. 7 (1), pp. 43. Date of Electronic Publication: 2022 Jul 22.
Publication Year :
2022

Abstract

Adiponectin, encoded by ADIPOQ, is an insulin-sensitizing, anti-inflammatory, and renoprotective adipokine that activates receptors with intrinsic ceramidase activity. We identified a family harboring a 10-nucleotide deletion mutation in ADIPOQ that cosegregates with diabetes and end-stage renal disease. This mutation introduces a frameshift in exon 3, resulting in a premature termination codon that disrupts translation of adiponectin's globular domain. Subjects with the mutation had dramatically reduced circulating adiponectin and increased long-chain ceramides levels. Functional studies suggest that the mutated protein acts as a dominant negative through its interaction with non-mutated adiponectin, decreasing circulating adiponectin levels, and correlating with metabolic disease.<br /> (© 2022. The Author(s).)

Details

Language :
English
ISSN :
2056-7944
Volume :
7
Issue :
1
Database :
MEDLINE
Journal :
NPJ genomic medicine
Publication Type :
Academic Journal
Accession number :
35869090
Full Text :
https://doi.org/10.1038/s41525-022-00314-z