DNA复制前染色体断裂

Dragovich Branko
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引用次数: 0

摘要

染色体断裂是电离辐射使细胞开放的更重要的结果之一,而且,可以肯定的是,电离辐射在造成这类潜在变化方面是最好的。另一种染色体畸形,除了破损,在遗传性疾病中很重要,但与辐射伤害无关,是染色体的不均匀分布,以至于小女孩的细胞错误地补充了没有缺陷的染色体。由于这最后的变化基本上不是辐射开放的显著结果,因此不再多说。染色体断裂可能发生在细胞DNA复制之前,在这种情况下,在复制过程中,潜在的缺陷同样会被重复(或者在努力复制过程中出现缺陷),在两条染色单体的中期染色体中会发现畸形。当DNA复制后发生断裂时,这种伤害在很大程度上被视为两条染色单体之一的不平衡变化。当大量分离细胞暴露在电离辐射下时,这些细胞处于细胞周期的所有潜在运动阶段。根据周期中受影响细胞的面积,可以发现染色体断裂导致的三种不同类型的染色体变异。其中的每一个都可以在中期染色体群中看到当细胞的一部分在细胞周期中向前推进到有丝分裂时。从光照到有丝分裂的时间将决定所观察到的细胞周期的情况。例如,对于一个给定的细胞系,当S时间框架的长度是6小时,G2M的长度是60分钟,在光照后7小时的有丝分裂分类将允许发生变化,这些变化是由于光照时几乎进入S时间框架的细胞的光照所导致的。光照后7小时聚集的细胞将拥有全部的能量来固定或潜在地补偿DNA。
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Chromosome Breakage before Replication of the DNA
Chromosome breakage is one of the more significant results of ionizing radiation openness of cells, and, to be sure, ionizing radiation is best in creating this class of underlying change. Another chromosome deformity, other than breakage, that is significant in hereditary illnesses, however that is irrelevant because of radiation harm, is maldistribution of chromosomes, to such an extent that little girl cells have a mistaken supplement of unblemished chromosomes. Since this last change is by and large not a significant result of radiation openness, no more will be said. Chromosome breakage can happen before replication of the DNA of the cell, in which occasion, at replication the underlying imperfection will likewise be repeated (or it will come up short in endeavored replication), and the deformity will be found in the metaphase chromosome in the two chromatids. At the point when breakage happens after DNA replication, the harm will for the most part be viewed as an unbalanced change in one of the two chromatids. As a populace of separating cells is presented to ionizing radiation, the cells are in all potential phases of movement through the cell cycle. Contingent upon the area of the influenced cell in the cycle, three distinct sorts of chromosome variations that outcome from chromosome breakage can be found. Every one of these will be seen in the metaphase chromosome cluster as that part of the cell populace advances forward through the cell cycle to mitosis. Time from the illumination occasion to the assortment of mitoses will decide the situation of the cell cycle that is noticed. For instance, for a given cell line, when the length of the S time frame is, say 6 hours and the length of G2M is 60 minutes, at that point assortment of mitoses at 7 hours after light will give admittance to changes that happened as the consequence of the illumination of cells that were nearly entering the S time frame at the hour of light. The cells gathered at 7 hours after illumination will possess had the entirety of this energy for fix or potentially compensation of DNA.
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