Zieve G W
J Cell Physiol. 1987 May;131(2):247-54. doi: 10.1002/jcp.1041310215.
The snRNAs are abundant and stable components of the interphase nucleus. Aqueous and non-aqueous cell fractionation demonstrate that the snRNAs appear transiently in the cytoplasm shortly after transcription, before returning permanently to the interphase nucleus. In pulse label and chase experiments, the newly synthesized snRNA species appear in the cytoplasm after 1 min of labeling and then return to the interphase nucleus after approximately 15 min in the cytoplasm. In order to study the maturation and intracellular transport of these particles, a battery of metabolic inhibitors and alterations in cell culture conditions were investigated for their ability to interfere with the return of the newly synthesized snRNAs to the nucleus. A wide range of inhibitors of the cytoskeleton did not interfere with this process. Only the inhibition of protein synthesis and exposure of cells to medium of at least twice the normal tonicity block the return of the snRNAs to the nucleus. Immunofluorescent staining of cells exposed to hypertonic medium identifies discrete foci in the cytoplasm that stain with the Sm antiserum, directed against proteins associated with the snRNAs. Using a detergent extraction procedure that preserves the cytoskeleton, the newly synthesized snRNAs in the cytoplasm fractionate as soluble complexes. These data are consistent with the hypothesis that the snRNAs partition into the interphase nucleus because of a preferential solubility and the existence of specific binding sites.
小核RNA(snRNAs)是间期细胞核中丰富且稳定的成分。水相和非水相细胞分级分离表明,snRNAs在转录后不久会短暂出现在细胞质中,然后再永久回到间期细胞核。在脉冲标记和追踪实验中,新合成的snRNA种类在标记1分钟后出现在细胞质中,然后在细胞质中大约15分钟后回到间期细胞核。为了研究这些颗粒的成熟和细胞内运输,研究了一系列代谢抑制剂以及细胞培养条件的改变对干扰新合成的snRNAs回到细胞核能力的影响。多种细胞骨架抑制剂并未干扰这一过程。只有蛋白质合成的抑制以及将细胞暴露于至少两倍正常张力的培养基中会阻止snRNAs回到细胞核。对暴露于高渗培养基的细胞进行免疫荧光染色,可在细胞质中识别出离散的焦点,这些焦点会被针对与snRNAs相关蛋白质的Sm抗血清染色。使用一种保留细胞骨架的去污剂提取程序,细胞质中新合成的snRNAs会分离为可溶性复合物。这些数据与以下假设一致,即snRNAs由于优先溶解性和特定结合位点的存在而分配到间期细胞核中。