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双形态梯度的分区模型。

A compartmental model for the bicoid gradient.

机构信息

Department of Chemical Engineering, Princeton University, Princeton, NJ, USA.

出版信息

Dev Biol. 2010 Sep 1;345(1):12-7. doi: 10.1016/j.ydbio.2010.05.491. Epub 2010 May 24.

Abstract

The anterior region of the Drosophila embryo is patterned by the concentration gradient of the homeodomain transcription factor bicoid (Bcd). The Bcd gradient was the first identified morphogen gradient and continues to be a subject of intense research at multiple levels, from the mechanisms of RNA localization in the oocyte to the evolution of the Bcd-mediated patterning events in multiple Drosophila species. Critical assessment of the mechanisms of the Bcd gradient formation requires biophysical models of the syncytial embryo. Most of the proposed models rely on reaction-diffusion equations, but their formulation and applicability at high nuclear densities is a nontrivial task. We propose a straightforward alternative in which the syncytial blastoderm is approximated by a periodic arrangement of well-mixed compartments: a single nucleus and an associated cytoplasmic region. We formulate a compartmental model, constrain its parameters by experimental data, and demonstrate that it provides an adequate description of the Bcd gradient dynamics.

摘要

果蝇胚胎的前区域由同源域转录因子bicoid(Bcd)的浓度梯度来定型。Bcd 梯度是第一个被识别的形态发生梯度,并且仍然是多个层次的激烈研究的主题,从卵母细胞中 RNA 定位的机制到多个果蝇物种中 Bcd 介导的模式形成事件的进化。对 Bcd 梯度形成机制的批判性评估需要合胞胚胎的生物物理模型。大多数提出的模型依赖于反应扩散方程,但在高核密度下的公式化和适用性是一个非平凡的任务。我们提出了一个简单的替代方案,其中合胞胚层通过均匀混合的隔室的周期性排列来近似:一个单独的核和一个相关的细胞质区域。我们制定了一个隔室模型,通过实验数据约束其参数,并证明它提供了对 Bcd 梯度动力学的充分描述。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/622b/2919596/93cbd2796cce/nihms209639f1.jpg

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Determining the scale of the Bicoid morphogen gradient.确定形态发生素Bicoid梯度的规模。
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