Daniele Joseph R, Chu Tehyen, Kunes Sam
Department of Molecular & Cellular Biology, Harvard University, 16 Divinity Avenue, Cambridge, MA 02138, USA
Department of Molecular & Cellular Biology, Harvard University, 16 Divinity Avenue, Cambridge, MA 02138, USA.
Biol Open. 2017 May 15;6(5):540-550. doi: 10.1242/bio.024083.
The patterning activity of a morphogen depends on secretion and dispersal mechanisms that shape its distribution to the cells of a receptive field. In the case of the protein Hedgehog (Hh), these mechanisms of secretion and transmission remain unclear. In the developing visual system, Hh is partitioned for release at opposite poles of photoreceptor neurons. Release into the retina regulates the progression of eye development; axon transport and release at axon termini trigger the development of postsynaptic neurons in the brain. Here we show that this binary targeting decision is controlled by a C-terminal proteolysis. Hh with an intact C-terminus undergoes axonal transport, whereas a C-terminal proteolysis enables Hh to remain in the retina, creating a balance between eye and brain development. Thus, we define a novel mechanism for the apical/basal targeting of this developmentally important protein and posit that similar post-translational regulation could underlie the polarity of related ligands.
形态发生素的模式形成活动取决于分泌和扩散机制,这些机制决定了其在感受野细胞中的分布形式。就蛋白质刺猬索尼克(Hh)而言,其分泌和传递机制仍不清楚。在发育中的视觉系统中,Hh被分隔开来,以便在感光神经元的相对两极释放。释放到视网膜中可调节眼睛发育进程;轴突运输以及在轴突末端的释放会触发大脑中突触后神经元的发育。在此,我们表明这种二元靶向决定是由C末端蛋白水解控制的。具有完整C末端的Hh会进行轴突运输,而C末端蛋白水解则使Hh保留在视网膜中,从而在眼睛和大脑发育之间建立平衡。因此,我们定义了一种针对这种对发育至关重要的蛋白质的顶端/基部靶向的新机制,并推测类似的翻译后调控可能是相关配体极性的基础。