Barrack E R
Department of Urology, Johns Hopkins University School of Medicine, Baltimore, MD 21205.
J Steroid Biochem. 1987;27(1-3):115-21. doi: 10.1016/0022-4731(87)90302-5.
The nuclear matrix is a conceptually attractive candidate for the site in the nucleus where steroid hormone-receptor complexes might interact to modulate DNA structure and function. We have demonstrated that in sex steroid target tissues a major proportion (50-100%) of the high affinity and steroid-specific receptors that become associated with the nucleus following hormonal stimulation are localized in the nuclear matrix. Direct cell-free binding assays confirm that this localization is due to the presence of specific acceptor sites in the matrix to which steroid-receptor complexes bind with high affinity and tissue specificity, and is not the result of spurious binding. The nuclear matrix appears to be a major site of hormone receptor binding in the nucleus, and this situation is consistent with the known ability of steroid hormones to stimulate gene transcription, a process which also appears to occur in association with the nuclear matrix.
核基质在概念上是类固醇激素受体复合物可能相互作用以调节DNA结构和功能的细胞核位点的一个有吸引力的候选者。我们已经证明,在性类固醇靶组织中,激素刺激后与细胞核结合的高亲和力和类固醇特异性受体的主要部分(50-100%)定位于核基质中。直接的无细胞结合试验证实,这种定位是由于基质中存在特异性受体位点,类固醇-受体复合物与之以高亲和力和组织特异性结合,而不是虚假结合的结果。核基质似乎是细胞核中激素受体结合的主要位点,这种情况与类固醇激素刺激基因转录的已知能力一致,而这一过程似乎也与核基质相关。