Any feedback?
Please rate this page
(literature.php)
(0/150)

BRENDA support

Literature summary for 1.14.99.66 extracted from

  • Hino, S.; Sakamoto, A.; Nagaoka, K.; Anan, K.; Wang, Y.; Mimasu, S.; Umehara, T.; Yokoyama, S.; Kosai, K.; Nakao, M.
    FAD-dependent lysine-specific demethylase-1 regulates cellular energy expenditure (2012), Nat. Commun., 3, 758 .
    View publication on PubMedView publication on EuropePMC

Organism

Organism UniProt Comment Textmining
Mus musculus Q6ZQ88
-
-

Source Tissue

Source Tissue Comment Organism Textmining
adipocyte
-
Mus musculus
-

Synonyms

Synonyms Comment Organism
KDM1A
-
Mus musculus

General Information

General Information Comment Organism
physiological function the inhibition of LSD1 activates energy-expenditure genes by transcriptional and epigenetic mechanisms in adipocytes. Disruption of LSD1 function results in the derepression of these genes leading to the activation of mitochondrial respiration and lipolysis in adipocytes. LSD1-mediated tranxadscriptional repression is FAD-dependent, and the disruption of cellular FAD synthesis exerts similar effects on the metabolic gene expression as the LSD1 inhibition. The expression of LSD1-target genes is markedly repressed in high fat-exposed white adipose tissue, and can be reverted by LSD1 inhibition Mus musculus