果蝇早期发育过程中基因/蛋白相互作用网络的随机时空动态模型。

Gene regulation and systems biology Pub Date : 2009-10-19
Cheng-Wei Li, Bor-Sen Chen
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引用次数: 0

摘要

为了探讨果蝇胚胎中均匀条纹形成的可能机制,本文建立了一个时空基因/蛋白质相互作用网络模型,模拟了果蝇胚胎中蛋白质合成、蛋白质衰变、mRNA衰变、蛋白质扩散、转录调控和自调节等动态行为,分析了果蝇胚胎早期不同区室中基因和蛋白质的相互作用。本研究利用最大似然(ML)方法,通过三维mRNA和蛋白质表达数据,识别基因/蛋白质相互作用网络的随机三维胚胎时空(3-DEST)动态模型,并利用赤池信息准则(AIC)对基因/蛋白质相互作用网络进行剪接。基因/蛋白相互作用网络的发现不仅使我们能够分析均匀条纹边缘基因和蛋白质的动态相互作用,而且还可以推断均匀条纹是由早期胚胎发生中转录调控和扩散机制共同构建的网络基序建立和维持的。文献参考和基因突变湿实验为验证所识别的网络提供了线索。所提出的时空动态模型可以扩展到不同生物表型的基因/蛋白网络构建,这些表型依赖于室室,例如出生后干细胞/祖细胞分化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Stochastic spatio-temporal dynamic model for gene/protein interaction network in early Drosophila development.

Stochastic spatio-temporal dynamic model for gene/protein interaction network in early Drosophila development.

Stochastic spatio-temporal dynamic model for gene/protein interaction network in early Drosophila development.

Stochastic spatio-temporal dynamic model for gene/protein interaction network in early Drosophila development.

In order to investigate the possible mechanisms for eve stripe formation of Drosophila embryo, a spatio-temporal gene/protein interaction network model is proposed to mimic dynamic behaviors of protein synthesis, protein decay, mRNA decay, protein diffusion, transcription regulations and autoregulation to analyze the interplay of genes and proteins at different compartments in early embryogenesis. In this study, we use the maximum likelihood (ML) method to identify the stochastic 3-D Embryo Space-Time (3-DEST) dynamic model for gene/protein interaction network via 3-D mRNA and protein expression data and then use the Akaike Information Criterion (AIC) to prune the gene/protein interaction network. The identified gene/protein interaction network allows us not only to analyze the dynamic interplay of genes and proteins on the border of eve stripes but also to infer that eve stripes are established and maintained by network motifs built by the cooperation between transcription regulations and diffusion mechanisms in early embryogenesis. Literature reference with the wet experiments of gene mutations provides a clue for validating the identified network. The proposed spatio-temporal dynamic model can be extended to gene/protein network construction of different biological phenotypes, which depend on compartments, e.g. postnatal stem/progenitor cell differentiation.

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