Traub P, Mothes E, Shoeman R L, Schröder R, Scherbarth A
Max-Planck-Institut für Zellbiologie, Rosenhof, Ladenburg bei Heidelberg, Federal Republic of Germany.
J Biomol Struct Dyn. 1992 Dec;10(3):505-31. doi: 10.1080/07391102.1992.10508665.
Guanine-rich polynucleotides such as poly(dG), oligo(dG)12-18 or poly(rG) were shown to exert a strong inhibitory effect on vimentin filament assembly and also to cause disintegration of preformed filaments in vitro. Gold-labeled oligo(dG)25 was preferentially localized at the physical ends of the aggregation and disaggregation products and at sites along filaments with a basic periodicity of 22.7 nm. Similar effects were observed with heat-denatured eukaryotic nuclear DNA or total rRNA, although these nucleic acids could affect filament formation and structure only at ionic strengths lower than physiological. However, whenever filaments were formed or stayed intact, they appeared associated with the nucleic acids. These electron microscopic observations were corroborated by sucrose gradient analysis of complexes obtained from preformed vimentin filaments and radioactively labeled heteroduplexes. Among the duplexes of the DNA type, particularly poly(dG).poly(dC), and, of those of the RNA type, preferentially poly(rA).poly(rU), were carried by the filaments with high efficiency into the pellet fraction. Single-stranded 18S and 28S rRNA interacted only weakly with vimentin filaments. Nevertheless, in a mechanically undisturbed environment, vimentin filaments could be densely decorated with intact 40S and 60S ribosomal subunits as revealed by electron microscopy. These results indicate that, in contrast to single-stranded nucleic acids with their compact random coil configuration, double-stranded nucleic acids with their elongated and flexible shape have the capability to stably interact with the helically arranged, surface-exposed amino-terminal polypeptide chains of vimentin filaments. Such interactions might be of physiological relevance in regard to the transport and positioning of nucleic acids and nucleoprotein particles in the various compartments of eukaryotic cells. Conversely, nucleic acids might be capable of affecting the cytoplasmic organization of vimentin filament networks through their filament-destabilizing potentials.
富含鸟嘌呤的多核苷酸,如聚(dG)、寡聚(dG)12 - 18或聚(rG),在体外对波形蛋白丝组装具有强烈抑制作用,还能导致预制丝解体。金标记的寡聚(dG)25优先定位在聚集和解聚产物的物理末端以及沿丝的具有22.7nm基本周期的位点。热变性的真核细胞核DNA或总rRNA也观察到类似效应,尽管这些核酸仅在离子强度低于生理值时才会影响丝的形成和结构。然而,只要丝形成或保持完整,它们似乎就与核酸相关。这些电子显微镜观察结果通过对从预制波形蛋白丝和放射性标记异源双链体获得的复合物进行蔗糖梯度分析得到了证实。在DNA类型的双链体中,特别是聚(dG)·聚(dC),而在RNA类型的双链体中,优先是聚(rA)·聚(rU),能被丝高效携带到沉淀部分。单链18S和28S rRNA与波形蛋白丝的相互作用较弱。尽管如此,在机械未受干扰的环境中,电子显微镜显示波形蛋白丝可被完整的40S和60S核糖体亚基密集装饰。这些结果表明,与具有紧密无规卷曲构象的单链核酸不同,具有细长且灵活形状的双链核酸有能力与波形蛋白丝螺旋排列、表面暴露的氨基末端多肽链稳定相互作用。这种相互作用在真核细胞不同区室中核酸和核蛋白颗粒的运输与定位方面可能具有生理相关性。相反,核酸可能通过其破坏丝稳定性的潜能影响波形蛋白丝网络的细胞质组织。