A nucleostemin family GTPase, NS3, acts in serotonergic neurons to regulate insulin signaling and control body size

被引:78
作者
Kaplan, Daniel D. [1 ,2 ,3 ]
Zimmermann, Gregor [1 ,2 ,3 ]
Suyama, Kaye [1 ,2 ,3 ]
Meyer, Tobias [4 ]
Scott, Matthew P. [1 ,2 ,3 ]
机构
[1] Stanford Univ, Sch Med, Howard Hughes Med Inst, Dept Dev Biol, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Howard Hughes Med Inst, Dept Genet, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Howard Hughes Med Inst, Dept Bioengn, Stanford, CA 94305 USA
[4] Stanford Univ, Sch Med, Dept Chem & Syst Biol, Stanford, CA 94305 USA
关键词
nucleostemin; serotonin; insulin; neurons; growth; size;
D O I
10.1101/gad.1670508
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Growth and body size are regulated by the CNS, integrating the genetic developmental program with assessments of an animal's current energy state and environmental conditions. CNS decisions are transmitted to all cells of the animal by insulin/insulin-like signals. The molecular biology of the CNS growth control system has remained, for the most part, elusive. Here we identify NS3, a Drosophila nucleostemin family GTPase, as a powerful regulator of body size. ns3 mutants reach < 60% of normal size and have fewer and smaller cells, but exhibit normal body proportions. NS3 does not act cell-autonomously, but instead acts at a distance to control growth. Rescue experiments were performed by expressing wild-type ns3 in many different cells of ns3 mutants. Restoring NS3 to only 106 serotonergic neurons rescued global growth defects. These neurons are closely apposed with those of insulin-producing neurons, suggesting possible communication between the two neuronal systems. In the brains of ns3 mutants, excess serotonin and insulin accumulate, while peripheral insulin pathway activation is low. Peripheral insulin pathway activation rescues the growth defects of ns3 mutants. The findings suggest that NS3 acts in serotonergic neurons to regulate insulin signaling and thus exert global growth control.
引用
收藏
页码:1877 / 1893
页数:17
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