Dysregulation of a long noncoding RNA reduces leptin leading to a leptin-responsive form of obesity.

TitreDysregulation of a long noncoding RNA reduces leptin leading to a leptin-responsive form of obesity.
Publication TypeJournal Article
Year of Publication2019
AuthorsDallner, OS, Marinis, JM, Lu, Y-H, Birsoy, K, Werner, E, Fayzikhodjaeva, G, Dill, BD, Molina, H, Moscati, A, Kutalik, Z, Marques-Vidal, P, Kilpeläinen, TO, Grarup, N, Linneberg, A, Zhang, Y, Vaughan, R, Loos, RJF, Lazar, MA, Friedman, JM
JournalNature medicine
Date Published03/2019
Mots-clésAnimals, Body Weight/drug effects, Body Weight/genetics, Diet, Eating/drug effects, Eating/genetics, Enhancer Elements, Female, Gene Expression Regulation, Genetic/genetics, High-Fat, Humans, Knockout, Leptin/genetics, Leptin/metabolism, Leptin/pharmacology, Long Noncoding/genetics, Male, Mice, Obesity/genetics, Obesity/metabolism, polymorphism, RNA, Single Nucleotide, Transgenic

Quantitative changes in leptin concentration lead to alterations in food intake and body weight, but the regulatory mechanisms that control leptin gene expression are poorly understood. Here we report that fat-specific and quantitative leptin expression is controlled by redundant cis elements and trans factors interacting with the proximal promoter together with a long noncoding RNA (lncOb). Diet-induced obese mice lacking lncOb show increased fat mass with reduced plasma leptin levels and lose weight after leptin treatment, whereas control mice do not. Consistent with this finding, large-scale genetic studies of humans reveal a significant association of single-nucleotide polymorphisms (SNPs) in the region of human lncOb with lower plasma leptin levels and obesity. These results show that reduced leptin gene expression can lead to a hypoleptinemic, leptin-responsive form of obesity and provide a framework for elucidating the pathogenic mechanism in the subset of obese patients with low endogenous leptin levels.

Alternate URL




Alternate JournalNat. Med.
Citation Key / SERVAL ID9433
Peer reviewRefereed
PubMed ID30842678


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