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Literature summary for 2.5.1.46 extracted from

  • Levasseur, E.M.; Yamada, K.; Pineros, A.R.; Wu, W.; Syed, F.; Orr, K.S.; Anderson-Baucum, E.; Mastracci, T.L.; Maier, B.; Mosley, A.L.; Liu, Y.; Bernal-Mizrachi, E.; Alonso, L.C.; Scott, D.; Garcia-Ocana, A.; Tersey, S.A.; Mirmira, R.G.
    Hypusine biosynthesis in beta cells links polyamine metabolism to facultative cellular proliferation to maintain glucose homeostasis (2019), Sci. Signal., 12, eaax0715 .
    View publication on PubMed

Organism

Organism UniProt Comment Textmining
Mus musculus Q3TXU5
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General Information

General Information Comment Organism
physiological function in a mouse model that enables the inducible, postnatal deletion of Dhps specifically in postnatal islet beta cells, removal of Dhps does not have an effect under normal physiologic conditions. Upon development of insulin resistance, which induces beta-cell proliferation, Dhps deletion causes alterations in proteins required for mRNA translation and protein secretion, reduced production of the cell cycle molecule cyclin D2, impaired beta-cell proliferation, and induces overt diabetes. Hypusine biosynthesis is downstream of protein kinase C-zeta and is required for c-Myc-induced proliferation Mus musculus