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2
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Quantitative Morphological Variation in the Developing Wing.发育中翅膀的定量形态变异
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The phosphoinositide phosphatase Sac1 regulates cell shape and microtubule stability in the developing eye.磷酸肌醇磷酸酶 Sac1 调节发育中眼睛的细胞形状和微管稳定性。
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本文引用的文献

1
Fast cloning inverted repeats for RNA interference.用于RNA干扰的快速克隆反向重复序列。
RNA. 2006 Nov;12(11):2020-4. doi: 10.1261/rna.258406. Epub 2006 Sep 27.
2
Identification of the death zone: a spatially restricted region for programmed cell death that sculpts the fly eye.死亡区域的识别:一个用于程序性细胞死亡的空间受限区域,它塑造了果蝇的眼睛。
Cell Death Differ. 2007 Feb;14(2):209-17. doi: 10.1038/sj.cdd.4401947. Epub 2006 May 19.
3
Csk-deficient boundary cells are eliminated from normal Drosophila epithelia by exclusion, migration, and apoptosis.缺乏Csk的边界细胞通过排斥、迁移和凋亡从正常果蝇上皮中被清除。
Dev Cell. 2006 Jan;10(1):33-44. doi: 10.1016/j.devcel.2005.11.007.
4
Shaping BMP morphogen gradients in the Drosophila embryo and pupal wing.在果蝇胚胎和蛹翅中塑造骨形态发生蛋白形态发生素梯度。
Development. 2006 Jan;133(2):183-93. doi: 10.1242/dev.02214.
5
Regulation of cell proliferation by a morphogen gradient.形态发生素梯度对细胞增殖的调控。
Cell. 2005 Nov 4;123(3):449-61. doi: 10.1016/j.cell.2005.08.030.
6
DPP signaling controls development of the lamina glia required for retinal axon targeting in the visual system of Drosophila.DPP信号通路控制果蝇视觉系统中视网膜轴突靶向所需的板层神经胶质细胞的发育。
Development. 2005 Oct;132(20):4587-98. doi: 10.1242/dev.02040. Epub 2005 Sep 21.
7
Preferential adhesion mediated by Hibris and Roughest regulates morphogenesis and patterning in the Drosophila eye.由Hibris和Roughest介导的优先黏附调节果蝇眼睛的形态发生和模式形成。
Dev Cell. 2005 Jun;8(6):925-35. doi: 10.1016/j.devcel.2005.03.011.
8
Extracellular signals responsible for spatially regulated proliferation in the differentiating Drosophila eye.负责果蝇分化眼中空间调控增殖的细胞外信号。
Dev Cell. 2005 Apr;8(4):541-51. doi: 10.1016/j.devcel.2005.01.017.
9
IrreC/rst-mediated cell sorting during Drosophila pupal eye development depends on proper localisation of DE-cadherin.果蝇蛹期眼睛发育过程中由IrreC/rst介导的细胞分选依赖于DE-钙黏蛋白的正确定位。
Development. 2005 May;132(9):2035-45. doi: 10.1242/dev.01800. Epub 2005 Mar 23.
10
Extrusion of cells with inappropriate Dpp signaling from Drosophila wing disc epithelia.来自果蝇翅盘上皮细胞中具有不适当Dpp信号传导的细胞挤出。
Science. 2005 Mar 18;307(5716):1789-90. doi: 10.1126/science.1104784.

动态的截瘫信号调控果蝇蛹视网膜的模式形成和黏附。

Dynamic decapentaplegic signaling regulates patterning and adhesion in the Drosophila pupal retina.

作者信息

Cordero Julia B, Larson David E, Craig Caroline R, Hays Rebecca, Cagan Ross

机构信息

Department of Molecular Biology and Pharmacology, Washington University School of Medicine, 660 South Euclid Avenue, Saint Louis, MO 63110, USA.

出版信息

Development. 2007 May;134(10):1861-71. doi: 10.1242/dev.002972. Epub 2007 Apr 11.

DOI:10.1242/dev.002972
PMID:17428827
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2957290/
Abstract

The correct organization of cells within an epithelium is essential for proper tissue and organ morphogenesis. The role of Decapentaplegic/Bone morphogenetic protein (Dpp/BMP) signaling in cellular morphogenesis during epithelial development is poorly understood. In this paper, we used the developing Drosophila pupal retina--looking specifically at the reorganization of glial-like support cells that lie between the retinal ommatidia--to better understand the role of Dpp signaling during epithelial patterning. Our results indicate that Dpp pathway activity is tightly regulated across time in the pupal retina and that epithelial cells in this tissue require Dpp signaling to achieve their correct shape and position within the ommatidial hexagon. These results point to the Dpp pathway as a third component and functional link between two adhesion systems, Hibris-Roughest and DE-cadherin. A balanced interplay between these three systems is essential for epithelial patterning during morphogenesis of the pupal retina. Importantly, we identify a similar functional connection between Dpp activity and DE-cadherin and Rho1 during cell fate determination in the wing, suggesting a broader link between Dpp function and junctional integrity during epithelial development.

摘要

上皮组织中细胞的正确组织对于正常的组织和器官形态发生至关重要。在表皮发育过程中,“十五体瘫”/骨形态发生蛋白(Dpp/BMP)信号在细胞形态发生中的作用尚不清楚。在本文中,我们利用发育中的果蝇蛹视网膜——特别关注位于视网膜小眼之间的胶质样支持细胞的重组——来更好地理解Dpp信号在上皮图案形成过程中的作用。我们的结果表明,Dpp信号通路在蛹视网膜中的活性随时间受到严格调控,并且该组织中的上皮细胞需要Dpp信号来在小眼六边形内获得正确的形状和位置。这些结果表明Dpp信号通路是两个黏附系统Hibris-Roughest和DE-钙黏蛋白之间的第三个组成部分和功能联系。这三个系统之间的平衡相互作用对于蛹视网膜形态发生过程中的上皮图案形成至关重要。重要的是,我们在翅的细胞命运决定过程中发现了Dpp活性与DE-钙黏蛋白和Rho1之间类似的功能联系,这表明在表皮发育过程中Dpp功能与连接完整性之间存在更广泛的联系。