Hendzel M J, Boisvert F, Bazett-Jones D P
Department of Cell Biology and Anatomy, Faculty of Medicine, University of Calgary, Calgary, Alberta, Canada T2N 4N1.
Mol Biol Cell. 1999 Jun;10(6):2051-62. doi: 10.1091/mbc.10.6.2051.
Whether the cell nucleus is organized by an underlying architecture analagous to the cytoskeleton has been a highly contentious issue since the original isolation of a nuclease and salt-resistant nuclear matrix. Despite electron microscopy studies that show that a nuclear architecture can be visualized after fractionation, the necessity to elute chromatin to visualize this structure has hindered general acceptance of a karyoskeleton. Using an analytical electron microscopy method capable of quantitative elemental analysis, electron spectroscopic imaging, we show that the majority of the fine structure within interchromatin regions of the cell nucleus in fixed whole cells is not nucleoprotein. Rather, this fine structure is compositionally similar to known protein-based cellular structures of the cytoplasm. This study is the first demonstration of a protein network in unfractionated and uninfected cells and provides a method for the ultrastructural characterization of the interaction of this protein architecture with chromatin and ribonucleoprotein elements of the cell nucleus.
自从最初分离出一种核酸酶和耐盐核基质以来,细胞核是否由类似于细胞骨架的潜在结构组织而成一直是一个极具争议的问题。尽管电子显微镜研究表明,分级分离后可以看到核结构,但为了观察这种结构而洗脱染色质的必要性阻碍了核骨架被普遍接受。使用一种能够进行定量元素分析的分析电子显微镜方法——电子光谱成像,我们发现固定的全细胞中细胞核染色质间区域内的大多数精细结构并非核蛋白。相反,这种精细结构在组成上类似于细胞质中已知的基于蛋白质的细胞结构。这项研究首次证明了未分级和未感染细胞中的蛋白质网络,并提供了一种超微结构表征这种蛋白质结构与细胞核染色质和核糖核蛋白元件相互作用的方法。