Nyman U, Hallman H, Hadlaczky G, Pettersson I, Sharp G, Ringertz N R
J Cell Biol. 1986 Jan;102(1):137-44. doi: 10.1083/jcb.102.1.137.
Anti-Sm antibodies recognize a group of small, nuclear RNA-protein complexes (snRNPs) containing U1, U2, U4, U5, and U6 snRNAs. Anti-RNP antibodies only react with U1 snRNA-containing complexes. The intranuclear distribution of snRNP particles was studied by double immunofluorescence staining of human fibroblasts. Mouse monoclonal anti-Sm antibodies and polyclonal patient sera reacting with different peptides in the snRNP complexes were used. The immunofluorescence patterns obtained with fluorescein isothiocyanate-conjugated anti-mouse Ig and tetramethylrhodamine isothiocyanate-conjugated anti-human Ig second antibodies were examined using computer analysis of digitized images. With this approach the similarity of different patterns could be visualized and estimated with mathematical methods. It was found that human anti-Sm serum as well as three different anti-RNP sera produced speckled patterns overlapping with the anti-Sm monoclonal pattern. Thus, Sm antigenic intranuclear domains also reacted with anti-RNP antibodies, suggesting a high degree of co-localization of the antigenic structures. A partial overlap was found between speckles detected by mouse anti-Sm antibodies and a human La-antiserum. No significant co-localization occurred between speckles detected by mouse anti-Sm antibodies and speckles detected by human antisera reacting with Scl-70 and centromeric antigens. As the U1 snRNP complex is believed to play a role in the splicing of RNA polymerase II transcripts, it appears that the speckles detected by Sm and RNP antibodies may be regions of hnRNA synthesis and mRNA processing. Although no function has been demonstrated for the U2, U4, U5, and U6 snRNPs, the co-localization with the U1 RNA complexes shown in this report indicate that they too participate in some aspect of mRNA processing. The results suggest that computer-assisted analysis of nuclear immunofluorescence patterns will be a useful tool in studies of the spatial and functional organization of the interphase nucleus.
抗Sm抗体识别一组包含U1、U2、U4、U5和U6小核RNA的小核核糖核蛋白复合体(snRNP)。抗RNP抗体仅与含U1 snRNA的复合体发生反应。通过对人成纤维细胞进行双重免疫荧光染色来研究snRNP颗粒的核内分布。使用了小鼠单克隆抗Sm抗体和与snRNP复合体中不同肽段反应的多克隆患者血清。使用计算机对数字化图像进行分析,检查用异硫氰酸荧光素偶联的抗小鼠Ig和异硫氰酸四甲基罗丹明偶联的抗人Ig二抗获得的免疫荧光模式。通过这种方法,可以用数学方法可视化并估计不同模式的相似性。发现人抗Sm血清以及三种不同的抗RNP血清产生的斑点模式与抗Sm单克隆模式重叠。因此,Sm抗原性核内结构域也与抗RNP抗体发生反应,表明抗原结构高度共定位。在小鼠抗Sm抗体检测到的斑点与人La抗血清检测到的斑点之间发现了部分重叠。在小鼠抗Sm抗体检测到的斑点与与Scl-70和着丝粒抗原反应的人抗血清检测到的斑点之间未发生明显的共定位。由于U1 snRNP复合体被认为在RNA聚合酶II转录本的剪接中起作用,因此似乎由Sm和RNP抗体检测到的斑点可能是hnRNA合成和mRNA加工的区域。尽管尚未证明U2、U4、U5和U6 snRNP具有功能,但本报告中显示的与U1 RNA复合体的共定位表明它们也参与了mRNA加工的某些方面。结果表明,计算机辅助分析核免疫荧光模式将成为研究间期细胞核空间和功能组织的有用工具。