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异源三聚体G蛋白的G12家族和Rho GTP酶介导音猬因子信号传导。

The G12 family of heterotrimeric G proteins and Rho GTPase mediate Sonic hedgehog signalling.

作者信息

Kasai Kenji, Takahashi Masanori, Osumi Noriko, Sinnarajah Srikumar, Takeo Tomohiro, Ikeda Hiroshi, Kehrl John H, Itoh Gen, Arnheiter Heinz

机构信息

Department of Pathology, Aichi Medical University School of Medicine, Nagakute, Aichi 480-1195, Japan.

出版信息

Genes Cells. 2004 Jan;9(1):49-58. doi: 10.1111/j.1356-9597.2004.00701.x.

Abstract

Sonic hedgehog (Shh) is a secreted morphogen crucial for cell fate decision, cellular proliferation, and patterning during vertebrate development. The intracellular Shh signalling is transduced by Smoothened (Smo), a seven-transmembrane spanning protein that belongs to the G-protein coupled receptor family. Among four families of Galpha subunits, Galphai has been thought to be responsible for transducing Shh signalling, while several lines of evidence indicated that other signalling pathways may be involved. We found that the G12 family of heterotrimeric G proteins and the small GTPase RhoA are involved in Shh/Smo-mediated cellular responses, including stimulation of target gene promoter and inhibition of neurite outgrowth of neuroblastoma cells. We also found that the G12/RhoA pathway is responsible for Smo-induced nuclear import of GLI3 which is thought to transduce Shh signals to nucleus. Furthermore, misexpression of a G12-specific GTPase-activating protein in rat neural tubes leads to pertubation of motor neurone and interneurone development, mimicking the effects of decreased Shh signalling. These results show that Shh signalling is mediated in part by activating G12 family coupled signalling pathways. The participation of RhoA, a pivotal molecular switch in many signal transduction pathways, may help explain how Shh can trigger a variety of cellular responses.

摘要

音猬因子(Shh)是一种分泌型形态发生素,对脊椎动物发育过程中的细胞命运决定、细胞增殖和模式形成至关重要。细胞内的Shh信号由Smoothened(Smo)转导,Smo是一种属于G蛋白偶联受体家族的七次跨膜蛋白。在Gα亚基的四个家族中,Gαi一直被认为负责转导Shh信号,而一些证据表明可能涉及其他信号通路。我们发现异源三聚体G蛋白的G12家族和小GTP酶RhoA参与了Shh/Smo介导的细胞反应,包括刺激靶基因启动子和抑制神经母细胞瘤细胞的神经突生长。我们还发现G12/RhoA途径负责Smo诱导的GLI3核转运,GLI3被认为将Shh信号转导至细胞核。此外,在大鼠神经管中错误表达G12特异性GTP酶激活蛋白会导致运动神经元和中间神经元发育紊乱,类似于Shh信号减少的影响。这些结果表明,Shh信号部分通过激活G12家族偶联信号通路介导。RhoA作为许多信号转导途径中的关键分子开关,其参与可能有助于解释Shh如何触发多种细胞反应。

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