Belmont A S, Bruce K
Department of Cell and Structural Biology, University of Illinois, Champaign-Urbana 61801.
J Cell Biol. 1994 Oct;127(2):287-302. doi: 10.1083/jcb.127.2.287.
We have used light microscopy and serial thin-section electron microscopy to visualize intermediates of chromosome decondensation during G1 progression in synchronized CHO cells. In early G1, tightly coiled 100-130-nm "chromonema" fibers are visualized within partially decondensed chromatin masses. Progression from early to middle G1 is accompanied by a progressive uncoiling and straightening of these chromonema fibers. Further decondensation in later G1 and early S phase results in predominantly 60-80-nm chromonema fibers that can be traced up to 2-3 microns in length as discrete fibers. Abrupt transitions in diameter from 100-130 to 60-80 nm along individual fibers are suggestive of coiling of the 60-80-nm chromonema fibers to form the thicker 100-130-nm chromonema fiber. Local unfolding of these chromonema fibers, corresponding to DNA regions tens to hundreds of kilobases in length, reveal more loosely folded and extended 30-nm chromatin fibers. Kinks and supercoils appear as prominent features at all observed levels of folding. These results are inconsistent with prevailing models of chromosome structure and, instead, suggest a folded chromonema model of chromosome structure.
我们利用光学显微镜和连续超薄切片电子显微镜,来观察同步化的中国仓鼠卵巢(CHO)细胞在G1期进程中染色体解聚的中间产物。在G1早期,在部分解聚的染色质团块中可观察到紧密盘绕的100 - 130纳米“染色线”纤维。从G1早期到中期的进程伴随着这些染色线纤维的逐渐解旋和伸直。在G1后期和S期早期的进一步解聚导致主要为60 - 80纳米的染色线纤维,这些纤维作为离散纤维可追踪到2 - 3微米长。沿着单个纤维直径从100 - 130纳米到60 - 80纳米的突然转变,提示60 - 80纳米的染色线纤维盘绕形成更粗的100 - 130纳米染色线纤维。这些染色线纤维的局部展开,对应于长度为数十到数百千碱基的DNA区域,揭示出折叠更松散且伸展的30纳米染色质纤维。纽结和超螺旋在所有观察到的折叠水平上都表现为突出特征。这些结果与当前的染色体结构模型不一致,相反,提示了一种染色体结构的折叠染色线模型。