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早期胚胎的结构复杂性:对线虫秀丽隐杆线虫的一项研究

Structural Complexity of Early Embryos: A Study on the Nematode Caenorhabditis elegans.

作者信息

Bignone F A

机构信息

Dept. Genetics and Biotechnology, I.S.T., National Cancer Institute, Lrgo. Rosanna Benzi, 10, 16123 Genova, Italy.

出版信息

J Biol Phys. 2001 Jun;27(2-3):257-83. doi: 10.1023/A:1013178514397.

Abstract

For analytical studies on the dynamics of gene expression, gene expressioncontrol and cellular interactions, the nematode Caenorhabditis elegans[C. elegans] is at present one of the best suited models [1-4].In this organism the genetic map and sequence is known [5], moreover theconstancy of its lineage tree allows a complete description of cellularclones giving rise to embryos. These characteristics have fostered detailedstudies on several aspects of development for this organism. Quantitativestudies of cellular movement, through time lapse cinematography of gastrulation, allows the description of cellular migrations giving rise to the final embryonic structure. In perspective, these studies coupledwith: genetic analysis, patterns of gene expression obtained throughmolecular techniques or other methods, open up the possibility of dynamicalstudies at the organismic scale. This possibility implies, first of all,a study of partitioning of space, and raise several problems in order todefine basic conceptual tools to be used in such studies. One of the mainproblems to handle in this respect is the definition of embryonic structurein a quantitative way. We will show that this aspect is a more generalcase of distance geometry approaches, as defined in protein folding studies.In this paper we discuss measures of the complexity for embryonal body plans,at the end of grastrulation. These can be applied to studies on the dynamicsof gene expression and phylogenetic studies with further experiments orsimulations.

摘要

对于基因表达动力学、基因表达调控和细胞相互作用的分析研究而言,线虫秀丽隐杆线虫[C. elegans]目前是最合适的模型之一[1-4]。在这种生物中,遗传图谱和序列是已知的[5],此外,其谱系树的恒定性使得能够完整描述产生胚胎的细胞克隆。这些特性促进了对该生物发育多个方面的详细研究。通过原肠胚形成的延时摄影对细胞运动进行定量研究,可以描述产生最终胚胎结构的细胞迁移。从长远来看,这些研究与遗传分析、通过分子技术或其他方法获得的基因表达模式相结合,开启了在生物体尺度上进行动力学研究的可能性。这种可能性首先意味着对空间划分的研究,并引发了几个问题,以便定义用于此类研究的基本概念工具。在这方面要处理的主要问题之一是以定量方式定义胚胎结构。我们将表明,这一方面是蛋白质折叠研究中定义的距离几何方法的一个更普遍的情况。在本文中,我们讨论了原肠胚形成末期胚胎体计划复杂性的度量。这些度量可应用于基因表达动力学研究以及通过进一步实验或模拟进行的系统发育研究。

相似文献

本文引用的文献

1
Mechanisms of protein folding.蛋白质折叠的机制。
Curr Opin Struct Biol. 2001 Feb;11(1):70-82. doi: 10.1016/s0959-440x(00)00176-7.

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