Ferguson M, Ward D C
Department of Molecular Biophysics, Yale University School of Medicine, New Haven, CT 06510.
Chromosoma. 1992 Aug;101(9):557-65. doi: 10.1007/BF00660315.
Fluorescent in situ hybridization with chromosome specific probes was used in conjunction with laser scanning confocal microscopy to assess the three-dimensional distribution of chromosomes in human T-lymphocyte nuclei. Cells in the G1-phase of the cell cycle exhibit a distinctly non-random chromosome organization:centromeric regions of the ten chromosomes examined are localized on the nuclear periphery, often making contact with the nuclear membrane, while telomeric domains are consistently localized within the interior 50% of the nuclear volume. Chromosome homolog pairing is not observed. Transition from the G1 to G2 cell cycle phase is accompanied by extensive chromosome movement, with centromeres assuming a more interior location. Chromosome condensation and chromatin depleted areas are observed in a small subset of G2 nuclei approaching mitosis. These results demonstrate that dynamic chromosome rearrangements occur in non-mitotic nuclei during the cell cycle.
使用与染色体特异性探针的荧光原位杂交技术,并结合激光扫描共聚焦显微镜,来评估人类T淋巴细胞核中染色体的三维分布。处于细胞周期G1期的细胞呈现出明显的非随机染色体组织:所检测的十条染色体的着丝粒区域位于核周边,常常与核膜接触,而端粒区域则始终位于核体积内部的50%范围内。未观察到染色体同源配对现象。从G1期到G2期的细胞周期转变伴随着广泛的染色体移动,着丝粒占据更靠内部的位置。在接近有丝分裂的一小部分G2核中观察到染色体凝聚和染色质缺失区域。这些结果表明,在细胞周期的非有丝分裂核中发生了动态染色体重排。