He D C, Nickerson J A, Penman S
Department of Biology, Beijing Normal University, Peoples Republic of China.
J Cell Biol. 1990 Mar;110(3):569-80. doi: 10.1083/jcb.110.3.569.
The nuclear matrix is concealed by a much larger mass of chromatin, which can be removed selectively by digesting nuclei with DNase I followed by elution of chromatin with 0.25 M ammonium sulfate. This mild procedure removes chromatin almost completely and preserves nuclear matrix morphology. The complete nuclear matrix consists of a nuclear lamina with an interior matrix composed of thick, polymorphic fibers and large masses that resemble remnant nucleoli. Further extraction of the nuclear matrices of HeLa or MCF-7 cells with 2 M sodium chloride uncovered a network of core filaments. A few dark masses remained enmeshed in the filament network and may be remnants of the nuclear matrix thick fibers and nucleoli. The highly branched core filaments had diameters of 9 and 13 nm measured relative to the intermediate filaments. They may serve as the core structure around which the matrix is constructed. The core filaments retained 70% of nuclear RNA. This RNA consisted both of ribosomal RNA precursors and of very high molecular weight hnRNA with a modal size of 20 kb. Treatment with RNase A removed the core filaments. When 2 M sodium chloride was used directly to remove chromatin after DNase I digestion without a preceding 0.25 M ammonium sulfate extraction, the core filaments were not revealed. Instead, the nuclear interior was filled with amorphous masses that may cover the filaments. This reflected a requirement for a stepwise increase in ionic strength because gradual addition of sodium chloride to a final concentration of 2 M without an 0.25 M ammonium sulfate extraction uncovered core filaments.
核基质被大量得多的染色质所掩盖,通过用DNA酶I消化细胞核,随后用0.25M硫酸铵洗脱染色质,可以选择性地去除染色质。这个温和的程序几乎完全去除了染色质,并保留了核基质的形态。完整的核基质由核纤层和内部基质组成,内部基质由粗大的、多形性的纤维和类似残留核仁的大块物质组成。用2M氯化钠进一步提取HeLa或MCF-7细胞的核基质,发现了一个核心细丝网络。一些深色物质仍缠绕在细丝网络中,可能是核基质粗纤维和核仁的残余物。相对于中间丝测量,高度分支的核心细丝直径为9纳米和13纳米。它们可能作为构建基质的核心结构。核心细丝保留了70%的核RNA。这种RNA既包括核糖体RNA前体,也包括分子量非常高的hnRNA,其模式大小为2万碱基对。用核糖核酸酶A处理可去除核心细丝。当在DNA酶I消化后直接用2M氯化钠去除染色质而不进行先前的0.25M硫酸铵提取时,未发现核心细丝。相反,核内部充满了可能覆盖细丝的无定形物质。这反映了对离子强度逐步增加的要求,因为在不进行0.25M硫酸铵提取的情况下,将氯化钠逐渐添加到最终浓度2M可发现核心细丝。