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

BRENDA support

Literature summary for 2.1.1.20 extracted from

  • Tain, L.S.; Jain, C.; Nespital, T.; Froehlich, J.; Hinze, Y.; Groenke, S.; Partridge, L.
    Longevity in response to lowered insulin signaling requires glycine N-methyltransferase-dependent spermidine production (2019), Aging Cell, 19, e13043 .
    View publication on PubMedView publication on EuropePMC

Organism

Organism UniProt Comment Textmining
Drosophila melanogaster Q9VG42
-
-
Mus musculus Q9QXF8
-
-

Source Tissue

Source Tissue Comment Organism Textmining
liver
-
Mus musculus
-

General Information

General Information Comment Organism
physiological function in the liver of liver-specific IRS1 KO mice, expression of GNMT is increased Mus musculus
physiological function reduced insulin/IGF signaling activity modulates methionine metabolism, through tissue-specific regulation of glycine N-methyltransferase Gnmt. This regulation is required for full insulin/IGF signaling-mediated longevity. Fat body-specific expression of Gnmt is sufficient to extend lifespan. Reducing insulin/IGF signaling activity leads to a Gnmt-dependent increase in spermidine levels. Both spermidine treatment and reduced insulin/IGF signaling activity are sufficient to extend the lifespan of Drosophila, but only in the presence of Gnmt Drosophila melanogaster