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不对称细胞分裂过程中Sara内体中的定向Delta和Notch运输

Directional Delta and Notch trafficking in Sara endosomes during asymmetric cell division.

作者信息

Coumailleau F, Fürthauer M, Knoblich J A, González-Gaitán M

机构信息

Department of Biochemistry, University of Geneva, 30 Quai Ernest-Ansermet, 1211 Geneva 4, Switzerland.

出版信息

Nature. 2009 Apr 23;458(7241):1051-5. doi: 10.1038/nature07854. Epub 2009 Mar 18.

Abstract

Endocytosis has a crucial role during Notch signalling after the asymmetric division of fly sensory organ precursors (SOPs): directional signalling is mediated by differential endocytosis of the ligand Delta and the Notch effector Sanpodo in one of the SOP daughters, pIIb. Here we show a new mechanism of directional signalling on the basis of the trafficking of Delta and Notch molecules already internalized in the SOP and subsequently targeted to the other daughter cell, pIIa. Internalized Delta and Notch traffic to an endosome marked by the protein Sara. During SOP mitosis, Sara endosomes containing Notch and Delta move to the central spindle and then to pIIa. Subsequently, in pIIa (but not in pIIb) Notch appears cleaved in Sara endosomes in a gamma-secretase- and Delta internalization-dependent manner, indicating that the release of the intracellular Notch tail to activate Notch target genes has occurred. We thus uncover a new mechanism to bias signalling even before asymmetric endocytosis of Sanpodo and Delta takes place in the daughter cells: already during SOP mitosis, asymmetric targeting of Delta and Notch-containing Sara endosomes will increase Notch signalling in pIIa and decrease it in pIIb.

摘要

在果蝇感觉器官前体细胞(SOP)不对称分裂后的Notch信号传导过程中,内吞作用起着至关重要的作用:在SOP的一个子代细胞pIIb中,配体Delta和Notch效应分子Sanpodo的差异性内吞介导了定向信号传导。在此,我们基于已经内化于SOP中并随后靶向至另一个子代细胞pIIa的Delta和Notch分子的运输,展示了一种定向信号传导的新机制。内化的Delta和Notch运输至由蛋白质Sara标记的内体。在SOP有丝分裂期间,含有Notch和Delta的Sara内体移动至纺锤体中部,然后移至pIIa。随后,在pIIa(而非pIIb)中,Notch在Sara内体中以γ-分泌酶和Delta内化依赖性方式出现裂解,这表明细胞内Notch尾巴的释放以激活Notch靶基因已经发生。因此,我们揭示了一种新机制,即在子代细胞中Sanpodo和Delta发生不对称内吞之前就使信号偏向:早在SOP有丝分裂期间,含有Delta和Notch的Sara内体的不对称靶向将增加pIIa中的Notch信号传导,并降低pIIb中的Notch信号传导。

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