遗传网络中的数学建模:基因表达与染色体断裂和正回路之间的关系

J. Aracena, S. Lamine, M. Mermet, O. Cohen, Jacques Demongeot
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引用次数: 22

摘要

人类基因组已经从一个原始的基因组进化到现在的状态,分布在23对染色体上。这种进化既受突变过程的支配,也受染色体内部或染色体之间基因组物质的生理和病理重组的支配,这些重组决定了基因组的变异性。这种重组始于染色体短臂或长臂上的奇异点,称为交叉、易位、插入或断点。在本文中,我们证明了这些点,也称为基因组的“弱点”或“热点”,是独立于它们的起源而相关的。此外,我们给出了相互作用矩阵在吸引子方面的一些性质(将先前的一些结果推广到离散情况)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mathematical modelling in genetic networks: relationships between the genetic expression and both chromosomic breakage and positive circuits
The human genome has evolved from a primitive genome to its present state dispatched along the 23 pairs of chromosomes. This evolution has been ruled by the mutation process and also by the physiological and pathological reorganization of the genomic material inside or between the chromosomes, which condition the genomic variability. This reorganization starts at singular points on the short or long chromosomic arms, called crossover, translocation, insertion or break-points. In this paper, we show that these points, also called "weak points" or "hot spots" of the genome, are correlated independently of their origin. In addition, we give some properties of the interaction matrices in terms of attractors (generalizing some earlier results to the discrete case).
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