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首页> 外文期刊>Journal of Microscopy >Statistical analysis of the three-dimensional structure of centromeric heterochromatin in interphase nuclei
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Statistical analysis of the three-dimensional structure of centromeric heterochromatin in interphase nuclei

机译:相间核着丝粒异染色质三维​​结构的统计分析

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Translocation of genes into the pericentromeric heterochromatin occurs during cellular differentiation and leads to a long-term silencing of these genes. Consequently, a structural remodelling of this heterochromatin compartment is observed during differentiation but this remains to be defined from a topological point of view. In a previous study, we analysed the three-dimensional (3D) distribution patterns of centromere clusters (chromocentres) by confocal scanning laser microscopy and found that differentiation of the promyelocytic leukaemia cell line NB4 along the neutrophil lineage is associated with a progressive clustering of centromeres. This clustering was reflected by a decreased number of detectable chromocentres, i.e. groups of centromeres with a distance below the diffraction-limited resolution of optical microscopy. The purpose of this study was to perform a statistical analysis of the 3D distribution of chromocentres in NB4 cells. Several point field characteristics (Ripley's K-function, L-function, pair correlation function, nearest-neighbour distribution function) were investigated to describe the topology of chromocentres during differentiation of NB4 cells. The pair correlation function revealed a higher frequency of chromocentre distances between 350 nm and 800 nm in undifferentiated NB4 cells as compared with differentiated cells. The L-function and the nearest-neighbour distribution function confirmed these results. These data imply the existence of intranuclear heterochromatin zones formed by functionally related centromeric regions. In view of the observed decrease in the number of detectable chromocentres during differentiation, we hypothesize that these zones with a diameter of 350-800 nm in undifferentiated NB4 cells contract into zones with a diameter below 350 nm in differentiated cells.
机译:基因向细胞着丝粒异染色质的移位发生在细胞分化过程中,并导致这些基因长期沉默。因此,在分化过程中观察到了该异染色质区室的结构重塑,但这仍需从拓扑学角度进行定义。在先前的研究中,我们通过共聚焦扫描激光显微镜分析了着丝粒簇(染色体中心)的三维(3D)分布模式,发现沿中性粒细胞谱系的早幼粒细胞白血病细胞系NB4的分化与着丝粒的逐步聚集有关。通过减少的可检测色心(即距离中心低于光学显微镜的衍射极限分辨率)的着丝粒组反映了这种聚集。这项研究的目的是对NB4细胞中色心的3D分布进行统计分析。研究了几个点场特征(Ripley的K函数,L函数,对相关函数,最近邻分布函数)来描述NB4细胞分化过程中发色中心的拓扑。该对相关函数显示,未分化的NB4细胞与分化细胞相比,在350 nm和800 nm之间有更高的发色中心距离频率。 L函数和最近邻分布函数证实了这些结果。这些数据暗示功能相关着丝粒区域形成的核内异染色质区的存在。鉴于观察到的分化过程中可检测到的色心数量减少,我们假设未分化的NB4细胞中直径为350-800 nm的这些区域收缩为分化细胞中直径低于350 nm的区域。

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