Herman R C, Williams J G, Penman S
Cell. 1976 Mar;7(3):429-37. doi: 10.1016/0092-8674(76)90173-2.
Highly purified steady state heterogeneous nuclear RNA from HeLa cells has been prepared by a new procedure. Detergent-washed nuclei are disrupted in 0.4 M ammonium sulfate, which also disociated contamination polysomes. The hnRNA remains bound to chromatin, which can be pelleted by gentle centrifugation. Ribonuclease inhibitors permit the preparation of very high molecular weight nuclear RNA. The hnRNA was cleaved with alkali. The poly(A)-containing fragments were separated from those containing oligo(A), and a cDNA copy was prepared. Hybridization of this nuclear cDNA to cytoplasmic mRNA showed that the scarce (complex) message sequences make up a larger proportion of nuclear RNA than of cytoplasmic RNA. In addition, at least 30% of the poly(A)-adjacent sequences in nuclear RNA have no apparent counterparts in the cytoplasm. cDNA prepared from hnRNA sedimenting faster than 45S under denaturing conditions gives similar results, showing the presence of both message and non-message sequences in very large transcripts. cDNA complementary to mRNA was separated into the abundant and scarce sequences, and hybridized separately to the poly(A)-adjacent sequences in nuclear RNA. The hybridization of the abundant sequence cDNA was used to set an upper limit on possible cytoplasmic contamination. Hybridization of the scarce cytoplasmic sequences are represented in nuclear RNA approximately once per cell.
通过一种新方法制备了来自HeLa细胞的高度纯化的稳态不均一核RNA。用去污剂洗涤过的细胞核在0.4M硫酸铵中破碎,硫酸铵也能解离污染的多核糖体。不均一核RNA仍与染色质结合,可通过轻轻离心沉淀。核糖核酸酶抑制剂使得能够制备非常高分子量的核RNA。用碱切割不均一核RNA。将含聚腺苷酸(poly(A))的片段与含寡聚腺苷酸(oligo(A))的片段分离,并制备了互补DNA(cDNA)拷贝。该核cDNA与细胞质信使核糖核酸(mRNA)杂交表明,稀少(复杂)的信使序列在核RNA中所占比例比在细胞质RNA中更大。此外,核RNA中至少30%的聚腺苷酸相邻序列在细胞质中没有明显的对应物。在变性条件下,从不均一核RNA中沉降速度快于45S的cDNA制备的cDNA给出了类似结果,表明在非常大的转录本中同时存在信使序列和非信使序列。与mRNA互补的cDNA被分离为丰富序列和稀少序列,并分别与核RNA中的聚腺苷酸相邻序列杂交。丰富序列cDNA的杂交用于设定可能的细胞质污染的上限。稀少细胞质序列的杂交在核RNA中大约每个细胞出现一次。