Long Non-Coding RNAs in Metabolic Organs and Energy Homeostasis.
Maude GiroudMarcel ScheidelerPublished in: International journal of molecular sciences (2017)
Single cell organisms can surprisingly exceed the number of human protein-coding genes, which are thus not at the origin of the complexity of an organism. In contrast, the relative amount of non-protein-coding sequences increases consistently with organismal complexity. Moreover, the mammalian transcriptome predominantly comprises non-(protein)-coding RNAs (ncRNA), of which the long ncRNAs (lncRNAs) constitute the most abundant part. lncRNAs are highly species- and tissue-specific with very versatile modes of action in accordance with their binding to a large spectrum of molecules and their diverse localization. lncRNAs are transcriptional regulators adding an additional regulatory layer in biological processes and pathophysiological conditions. Here, we review lncRNAs affecting metabolic organs with a focus on the liver, pancreas, skeletal muscle, cardiac muscle, brain, and adipose organ. In addition, we will discuss the impact of lncRNAs on metabolic diseases such as obesity and diabetes. In contrast to the substantial number of lncRNA loci in the human genome, the functionally characterized lncRNAs are just the tip of the iceberg. So far, our knowledge concerning lncRNAs in energy homeostasis is still in its infancy, meaning that the rest of the iceberg is a treasure chest yet to be discovered.
Keyphrases
- genome wide identification
- genome wide analysis
- network analysis
- skeletal muscle
- long non coding rna
- transcription factor
- single cell
- genome wide
- endothelial cells
- insulin resistance
- type diabetes
- magnetic resonance
- gene expression
- healthcare
- rna seq
- cardiovascular disease
- induced pluripotent stem cells
- poor prognosis
- adipose tissue
- amino acid
- heart failure
- binding protein
- protein protein
- weight gain
- left ventricular
- multiple sclerosis
- oxidative stress
- dna methylation
- pluripotent stem cells
- small molecule
- palliative care
- blood brain barrier
- gram negative
- heat shock protein