Long Noncoding RNAs in Diet-Induced Metabolic Diseases

被引:1
作者
Brandt, Annette [1 ]
Kopp, Florian [2 ]
机构
[1] Univ Vienna, Dept Nutr Sci, Mol Nutr Sci, A-1090 Vienna, Austria
[2] Univ Vienna, Dept Pharmaceut Sci, Clin Pharm Grp, A-1090 Vienna, Austria
关键词
lncRNA; long noncoding RNA; metabolic disease; hepatic steatosis; MASLD; NAFLD; type; 2; diabetes; obesity; FATTY LIVER-DISEASE; HEPATIC STEATOSIS; INDUCED OBESITY; GUT MICROBIOTA; RISK-FACTORS; LEPTIN; DYSREGULATION; TRANSCRIPTION; TRANSLATION; MECHANISMS;
D O I
10.3390/ijms25115678
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The prevalence of metabolic diseases, including type 2 diabetes and metabolic dysfunction-associated steatotic liver disease (MASLD), is steadily increasing. Although many risk factors, such as obesity, insulin resistance, or hyperlipidemia, as well as several metabolic gene programs that contribute to the development of metabolic diseases are known, the underlying molecular mechanisms of these processes are still not fully understood. In recent years, it has become evident that not only protein-coding genes, but also noncoding genes, including a class of noncoding transcripts referred to as long noncoding RNAs (lncRNAs), play key roles in diet-induced metabolic disorders. Here, we provide an overview of selected lncRNA genes whose direct involvement in the development of diet-induced metabolic dysfunctions has been experimentally demonstrated in suitable in vivo mouse models. We further summarize and discuss the associated molecular modes of action for each lncRNA in the respective metabolic disease context. This overview provides examples of lncRNAs with well-established functions in diet-induced metabolic diseases, highlighting the need for appropriate in vivo models and rigorous molecular analyses to assign clear biological functions to lncRNAs.
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页数:15
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