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首页> 外文期刊>Cellular Oncology: Analytical Cellular Pathology >Biphasic Chromatin Structure and FISH Signals Reflect Intranuclear Order
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Biphasic Chromatin Structure and FISH Signals Reflect Intranuclear Order

机译:双相染色质结构和FISH信号反映了核内顺序。

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Background and Aim: One of the two parental allelic genes may selectively be expressed, regulated by imprinting, X-inactivation or by other less known mechanisms. This study aims to reflect on such genetic mechanisms. Materials andMethods: Slides from short term cultures or direct smears of blood, bone marrow and amniotic fluids were hybridized with FISH probes singly, combined or sequentially. Two to three hundred cells were examined from each preparation.Results and Aignificance: A small number of cells (up to about 5%), more frequent in leukemia cases, showed the twin features: (1) nuclei with biphasic chromatin, one part decondensed and the other condensed; and (2) homologous FISH signals distributed equitably in those two regions. The biphasic chromatin structure with equitable distribution of the homologous FISH signals may correspond to the two sets of chromosomes, supporting observations on ploidywise intranuclear order. The decondensed chromatin may relate to enhanced transcriptions or advanced replications.Conclusions: Transcriptions of only one of the two parental genomes cause allelic exclusion. Genomes may switch with alternating monoallelic expression of biallelic genes as an efficient genetic mechanism. If genomes fail to switch, allelic exclusion may lead to malignancy. Similarly, a genome-wide monoallelic replication may tilt the balance of heterozygosity resulting in aneusomy, initiating early events in malignant transformation and in predicting cancer mortality.
机译:背景和目的:两个亲本等位基因之一可以通过表达,X灭活或其他鲜为人知的机制选择性表达,调控。这项研究旨在反思这种遗传机制。材料和方法:将短期培养的玻片或血液,骨髓和羊水的直接涂片与FISH探针单独,组合或顺序杂交。每种制剂检查了两到三百个细胞。结果和意义:少数细胞(最多约5%),在白血病病例中更常见,表现出双胞胎特征:(1)核具有双相染色质,一部分被浓缩另一个浓缩; (2)同源的FISH信号在这两个区域内均等分布。具有相等分布的同源FISH信号的双相染色质结构可能对应于两组染色体,从而支持了倍性核内顺序的观察。去浓缩的染色质可能与转录增强或高级复制有关。结论:两个亲本基因组中只有一个的转录导致等位基因排斥。基因组可能会交替转换双等位基因的单等位基因表达作为有效的遗传机制。如果基因组无法转换,则等位基因排斥可能导致恶性肿瘤。同样,全基因组的单等位基因复制可能会使杂合性的平衡倾斜,从而导致气肿,在恶性转化中引发早期事件并预测癌症死亡率。

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