Gollin S M, Wray W, Hanks S K, Hittelman W N, Rao P N
J Cell Sci Suppl. 1984;1:203-21. doi: 10.1242/jcs.1984.supplement_1.13.
In an effort to understand the arrangement of the basic 30 nm chromatin fibre within metaphase chromosomes, changes in the organization of prematurely condensed chromosomes (PCC) were examined as a function of progression through the cell cycle. The structural features of PCC observed under the light microscope were compared with those obtained by scanning electron microscopy. PCC with varying levels of condensation were obtained by fusing mitotic HeLa cells with interphase cells synchronized at different times in the cell cycle. PCC from G1 cells are composed of rather tightly packed bundles of tortuous chromatin fibres. The density of fibre packing along the longitudinal axis of G1-phase PCC is lower and less uniform than that of metaphase chromosomes. Early G1 PCC exhibit gyres suggesting a despiralized chromonema. The condensed domains in G1 PCC appear to be organized as supercoiled loops; whereas fibre-sparse domains consist of longitudinal fibres running along the chromosome axis. As cells progressed towards S phase, a greater proportion of highly extended regions containing prominent longitudinal fibres became evident in the PCC. The pulverized appearance of S-phase PCC under the light microscope corresponded to the highly condensed, looping fibre domains separated by more extended segments containing longitudinal fibres that are visualized using the scanning electron microscope. Active sites of DNA synthesis are implicated to be localized within extended longitudinal fibres. Post-replicative chromosome maturation extends through the G2 period and appears to involve rearrangement of the extended longitudinal fibres into packed looping-fibre clusters, which then coalesce. These observations support the model for packing DNA into chromosomes proposed in 1980 by Mullinger & Johnson. Briefly, this model suggests that the chromonema of each metaphase chromatid contains regions composed of folded longitudinal chromatin fibres as well as looping fibres that emerge from the axis at distinct foci. The final level of chromatin packing in metaphase chromosomes is attained by spiralization of the chromonema.
为了了解中期染色体中基本的30纳米染色质纤维的排列方式,研究了早熟凝集染色体(PCC)的组织变化与细胞周期进程的关系。将光学显微镜下观察到的PCC结构特征与扫描电子显微镜下获得的特征进行了比较。通过将有丝分裂的HeLa细胞与在细胞周期不同时间同步的间期细胞融合,获得了不同凝集水平的PCC。来自G1期细胞的PCC由相当紧密堆积的曲折染色质纤维束组成。G1期PCC纵轴上的纤维堆积密度低于中期染色体,且不如中期染色体均匀。早期G1期PCC呈现出螺旋状,表明染色线解螺旋。G1期PCC中的凝集区域似乎组织成超螺旋环;而纤维稀疏区域由沿染色体轴延伸的纵向纤维组成。随着细胞向S期进展,PCC中出现了更大比例的含有突出纵向纤维的高度伸展区域。光镜下S期PCC的粉碎外观对应于扫描电子显微镜下观察到的由更伸展的含有纵向纤维的片段分隔的高度凝集的环状纤维区域。DNA合成的活性位点被认为定位于伸展的纵向纤维内。复制后染色体成熟贯穿G2期,似乎涉及将伸展的纵向纤维重排为堆积的环状纤维簇,然后这些簇合并。这些观察结果支持了Mullinger和Johnson在1980年提出的将DNA包装成染色体的模型。简而言之,该模型表明每个中期染色单体的染色线包含由折叠的纵向染色质纤维以及从轴上不同位点出现的环状纤维组成的区域。中期染色体中染色质包装的最终水平是通过染色线的螺旋化实现的。