Fey E G, Ornelles D A, Penman S
Department of Biology, Massachusetts Institute of Technology, Cambridge 02139.
J Cell Sci Suppl. 1986;5:99-119. doi: 10.1242/jcs.1986.supplement_5.6.
Heteronuclear RNA (hnRNA) is preferentially associated (76%) with the nuclear matrix in mammalian cells. Active mRNA, in the form of polyribosomes, is associated (greater than 97%) with the cytoskeletal framework. In this report, we present evidence that the association of both hnRNA and mRNA with structural networks of the cell may be essential features of gene expression. To study the association of polyribosomes with the cytoskeletal framework, cytochalasin D was used to release mRNA from the cytoskeletal framework. Protein synthesis was inhibited by cytochalasin D in direct proportion to the release of mRNA. The released mRNA is unaltered in its translatability as measured in vitro but is no longer translated in the cytochalasin-treated HeLa cells. The residual protein synthesis occurs on polyribosomes that are reduced in amount but display a normal sedimentation distribution. The results support the hypothesis that mRNA binding to the cytoskeletal framework is necessary, though not sufficient, for translation. Further fractionation of the cytoskeletal framework separates nuclear constituents into three distinct protein fractions. Chromatin proteins and 94% of the DNA are released by 0.25 M-ammonium sulphate after inter-nucleosomal DNA is cut with DNase I. The resulting structure retains 76% of the hnRNA in the form of ribonucleoprotein and is designated the RNP-containing nuclear matrix. The proteins of hnRNP complex are those associated with the nucleus only if RNA is intact. These proteins and 97% of the hnRNA are released after brief digestion with RNase A. Visualizing the nuclear matrix using resinless sections shows that nuclear RNA plays an important role in the organization of the nuclear matrix. Electron micrographs of resinless sections show the interior of the matrix to be a three-dimensional network of thick filaments bounded by the nuclear lamina. The filaments are densely covered with 20-30 nm electron-dense particles, which may contain the hnRNA. The RNP-depleted matrix is disordered and the interior fibres aggregated. These results suggest that hnRNA is involved in the spatial organization of the interior of the nuclear matrix.
异核RNA(hnRNA)在哺乳动物细胞中优先与核基质结合(76%)。以多核糖体形式存在的活性mRNA与细胞骨架框架结合(大于97%)。在本报告中,我们提供证据表明,hnRNA和mRNA与细胞结构网络的结合可能是基因表达的基本特征。为了研究多核糖体与细胞骨架框架的结合,使用细胞松弛素D从细胞骨架框架中释放mRNA。细胞松弛素D抑制蛋白质合成的程度与mRNA的释放成正比。释放的mRNA在体外测量时其翻译能力未改变,但在经细胞松弛素处理的HeLa细胞中不再翻译。残留的蛋白质合成发生在数量减少但沉降分布正常的多核糖体上。这些结果支持了这样的假设,即mRNA与细胞骨架框架的结合对于翻译是必要的,但不是充分的。对细胞骨架框架进行进一步分级分离,可将核成分分离成三个不同的蛋白质组分。在用DNase I切割核小体间DNA后,0.25M硫酸铵可释放染色质蛋白和94%的DNA。所得结构以核糖核蛋白的形式保留76%的hnRNA,被称为含RNP的核基质。hnRNP复合物的蛋白质只有在RNA完整时才与细胞核相关。在用RNase A短暂消化后,这些蛋白质和97%的hnRNA被释放。使用无树脂切片观察核基质表明,核RNA在核基质的组织中起重要作用。无树脂切片的电子显微镜照片显示,基质内部是由核纤层界定的粗丝三维网络。这些细丝密集地覆盖着20 - 30nm的电子致密颗粒,其中可能含有hnRNA。不含RNP的基质无序,内部纤维聚集。这些结果表明,hnRNA参与核基质内部的空间组织。