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端粒长度维持替代机制的数学模型

Mathematical model of alternative mechanism of telomere length maintenance.

作者信息

Kollár Richard, Bod'ová Katarína, Nosek Jozef, Tomáška L'ubomír

机构信息

Department of Applied Mathematics and Statistics, Faculty of Mathematics, Physics, and Informatics, Comenius University, Mlynská dolina, 842 48 Bratislava, Slovakia.

Department of Applied Mathematics and Statistics, Faculty of Mathematics, Physics, and Informatics, Comenius University, Mlynská dolina, 842 48 Bratislava, Slovakia and Institute of Science and Technology, Am Campus 1, 3400 Klosterneuburg, Austria.

出版信息

Phys Rev E Stat Nonlin Soft Matter Phys. 2014 Mar;89(3):032701. doi: 10.1103/PhysRevE.89.032701. Epub 2014 Mar 4.

Abstract

Biopolymer length regulation is a complex process that involves a large number of biological, chemical, and physical subprocesses acting simultaneously across multiple spatial and temporal scales. An illustrative example important for genomic stability is the length regulation of telomeres-nucleoprotein structures at the ends of linear chromosomes consisting of tandemly repeated DNA sequences and a specialized set of proteins. Maintenance of telomeres is often facilitated by the enzyme telomerase but, particularly in telomerase-free systems, the maintenance of chromosomal termini depends on alternative lengthening of telomeres (ALT) mechanisms mediated by recombination. Various linear and circular DNA structures were identified to participate in ALT, however, dynamics of the whole process is still poorly understood. We propose a chemical kinetics model of ALT with kinetic rates systematically derived from the biophysics of DNA diffusion and looping. The reaction system is reduced to a coagulation-fragmentation system by quasi-steady-state approximation. The detailed treatment of kinetic rates yields explicit formulas for expected size distributions of telomeres that demonstrate the key role played by the J factor, a quantitative measure of bending of polymers. The results are in agreement with experimental data and point out interesting phenomena: an appearance of very long telomeric circles if the total telomere density exceeds a critical value (excess mass) and a nonlinear response of the telomere size distributions to the amount of telomeric DNA in the system. The results can be of general importance for understanding dynamics of telomeres in telomerase-independent systems as this mode of telomere maintenance is similar to the situation in tumor cells lacking telomerase activity. Furthermore, due to its universality, the model may also serve as a prototype of an interaction between linear and circular DNA structures in various settings.

摘要

生物聚合物长度调控是一个复杂的过程,涉及大量生物、化学和物理子过程,这些子过程在多个空间和时间尺度上同时起作用。对基因组稳定性很重要的一个例证是端粒的长度调控,端粒是线性染色体末端的核蛋白结构,由串联重复的DNA序列和一组特殊的蛋白质组成。端粒的维持通常由端粒酶促进,但特别是在无端粒酶的系统中,染色体末端的维持取决于由重组介导的端粒替代延长(ALT)机制。已确定各种线性和环状DNA结构参与ALT,然而,整个过程的动力学仍知之甚少。我们提出了一个ALT的化学动力学模型,其动力学速率是从DNA扩散和环化的生物物理学系统推导出来的。通过准稳态近似,反应系统简化为一个凝聚-破碎系统。对动力学速率的详细处理得出了端粒预期大小分布的明确公式,这些公式证明了J因子所起的关键作用,J因子是聚合物弯曲的定量度量。结果与实验数据一致,并指出了有趣的现象:如果总端粒密度超过临界值(过量质量),会出现非常长的端粒环,以及端粒大小分布对系统中端粒DNA量的非线性响应。这些结果对于理解无端粒酶系统中端粒的动力学可能具有普遍重要性,因为这种端粒维持模式与缺乏端粒酶活性的肿瘤细胞中的情况相似。此外,由于其普遍性,该模型还可作为各种情况下线性和环状DNA结构之间相互作用的原型。

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