S6K1 −/− / S6K2 −/− Mice Exhibit Perinatal Lethality and Rapamycin-Sensitive 5′-Terminal Oligopyrimidine mRNA Translation and Reveal a Mitogen-Activated Protein Kinase-Dependent S6 Kinase Pathway
Friedrich Miescher Institute · Cell Signaling Technology (United States) · +2 more institutions
Abstract
Activation of 40S ribosomal protein S6 kinases (S6Ks) is mediated by anabolic signals triggered by hormones, growth factors, and nutrients. Stimulation by any of these agents is inhibited by the bacterial macrolide rapamycin, which binds to and inactivates the mammalian target of rapamycin, an S6K kinase. In mammals, two genes encoding homologous S6Ks, S6K1 and S6K2, have been identified. Here we show that mice deficient for S6K1 or S6K2 are born at the expected Mendelian ratio. Compared to wild-type mice, S6K1(-/-) mice are significantly smaller, whereas S6K2(-/-) mice tend to be slightly larger. However, mice lacking both genes showed a sharp reduction in viability due to perinatal lethality. Analysis of S6…
Citation impact
- FWCI
- 17.96
- Percentile
- 100%
- References
- 68
Authors
10- MPMario PendeCorresponding
Friedrich Miescher Institute, Cell Signaling Technology (United States), Inserm
- SHSung Hee Um
Friedrich Miescher Institute
- VMVirginie Mieulet
Cell Signaling Technology (United States), Inserm
- MSMelanie Sticker
Friedrich Miescher Institute
- VLValerie L. Goss
Friedrich Miescher Institute, Cell Signaling Technology (United States)
Topics & keywords
- P70-S6 Kinase 1
- Biology
- Ribosomal protein s6
- Kinase
- Cell biology
- Protein kinase A
- Phosphorylation
- Ribosomal s6 kinase