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本文引用的文献

1
The bicoid morphogen system.双皮质形态发生素系统。
Curr Biol. 2010 Mar 9;20(5):R249-54. doi: 10.1016/j.cub.2010.01.026.
2
Fgf8 morphogen gradient forms by a source-sink mechanism with freely diffusing molecules.成纤维细胞生长因子8(Fgf8)形态发生素梯度通过源-汇机制与自由扩散分子形成。
Nature. 2009 Sep 24;461(7263):533-6. doi: 10.1038/nature08391. Epub 2009 Sep 9.
3
Determining the scale of the Bicoid morphogen gradient.确定形态发生素Bicoid梯度的规模。
Proc Natl Acad Sci U S A. 2009 Feb 10;106(6):1710-5. doi: 10.1073/pnas.0807655106. Epub 2009 Feb 3.
4
Formation of the bicoid morphogen gradient: an mRNA gradient dictates the protein gradient.双尾形态发生素梯度的形成:mRNA梯度决定蛋白质梯度。
Development. 2009 Feb;136(4):605-14. doi: 10.1242/dev.031195.
5
In vivo dynamics of Drosophila nuclear envelope components.果蝇核膜成分的体内动态变化
Mol Biol Cell. 2008 Sep;19(9):3652-66. doi: 10.1091/mbc.e07-11-1162. Epub 2008 Jun 18.
6
Shape and function of the Bicoid morphogen gradient in dipteran species with different sized embryos.不同胚胎大小双翅目物种中形态发生素Bicoid梯度的形状与功能
Dev Biol. 2008 Apr 15;316(2):350-8. doi: 10.1016/j.ydbio.2008.01.039. Epub 2008 Feb 13.
7
Re-examining the stability of the Bicoid morphogen gradient.重新审视形态发生素双尾蛋白梯度的稳定性。
Cell. 2008 Jan 11;132(1):15-7; author reply 17-8. doi: 10.1016/j.cell.2007.12.022.
8
Modeling the bicoid gradient: diffusion and reversible nuclear trapping of a stable protein.模拟双尾梯度:稳定蛋白质的扩散与可逆核捕获
Dev Biol. 2007 Dec 15;312(2):623-30. doi: 10.1016/j.ydbio.2007.09.058. Epub 2007 Oct 6.
9
Stability and nuclear dynamics of the bicoid morphogen gradient.双尾形态发生素梯度的稳定性与核动力学
Cell. 2007 Jul 13;130(1):141-52. doi: 10.1016/j.cell.2007.05.026.
10
Pre-steady-state decoding of the Bicoid morphogen gradient.形态发生素Bicoid梯度的稳态前解码
PLoS Biol. 2007 Feb;5(2):e46. doi: 10.1371/journal.pbio.0050046.

荧光相关光谱技术捕获的高迁移率的bicoid:对其快速建立梯度的启示。

High mobility of bicoid captured by fluorescence correlation spectroscopy: implication for the rapid establishment of its gradient.

机构信息

Department of Physics and Astronomy, McMaster University, Hamilton, Ontario, Canada.

出版信息

Biophys J. 2010 Aug 9;99(4):L33-5. doi: 10.1016/j.bpj.2010.05.031.

DOI:10.1016/j.bpj.2010.05.031
PMID:20712981
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2920644/
Abstract

The Bicoid (Bcd) morphogen is essential for pattern formation in fruit flies. It forms an exponential concentration gradient along the embryo AP axis and turns on cascades of target genes in distinct anterior domains. The most commonly accepted model for gradient formation assumes that Bcd travels by simple diffusion and is uniformly degraded across syncytial embryos, yet several recent studies have challenged these ideas. Here, the question of Bcd mobility was investigated using fluorescence correlation spectroscopy in live Drosophila melanogaster embryos. Bcd-EGFP molecules were found to be highly mobile in the cytoplasm during cycles 12-14, with a diffusion coefficient approximately 7 microm(2)/s. This value is large enough to explain the stable establishment of the Bcd gradient simply by diffusion before cycle 8, i.e., before the onset of zygotic transcription.

摘要

Bicoid (Bcd) 形态发生素对于果蝇的模式形成至关重要。它在胚胎 AP 轴上形成指数浓度梯度,并在前部区域中开启一系列靶基因级联反应。梯度形成的最常见模型假设 Bcd 通过简单扩散,并在合胞胚胎中均匀降解,然而最近的几项研究挑战了这些观点。在这里,使用荧光相关光谱法在活体黑腹果蝇胚胎中研究了 Bcd 的迁移性。发现 Bcd-EGFP 分子在周期 12-14 期间在细胞质中具有高度的流动性,扩散系数约为 7 微米 2/秒。这个值足以解释在周期 8 之前,即在合子转录开始之前,Bcd 梯度仅通过扩散就可以稳定建立。