Kozlov A P, Pliusnin A Z, Evgushenko V I, Seĭts I F
Biokhimiia. 1979 Jan;44(1):27-32.
An attempt was made to elucidate the possible participation of low molecular weight nuclear RNAs in the transcription process. The parameters of the RNA synthesis cell-free system in isolated rat liver nuclei were studied for this purpose. Tissue homogenization in isotonic sucrose during isolation of the nuclei resulted in a loss of 4S nuclear RNA. The dependence of RNA synthesis on the salt concentration in the incubation medium is indicative of possible initiation of the RNA synthesis in this system. At salt concentration of 0.08 M 50-75% of incorporation is due to the activity of RNA polymerase II. Under these conditions the electrophoretically homogenous individual fractions of low molecular weight nuclear RNAs do not affect specifically the activity of RNA polymerase II. No evidence for the participation of low molecular weight nuclear RNAs in the mechanisms of heterogeneous nuclear RNA synthesis were obtained.
人们试图阐明低分子量核RNA在转录过程中可能的参与情况。为此,研究了分离的大鼠肝细胞核中无细胞RNA合成系统的参数。在细胞核分离过程中,于等渗蔗糖中进行组织匀浆导致4S核RNA丢失。RNA合成对孵育培养基中盐浓度的依赖性表明该系统中可能启动了RNA合成。在盐浓度为0.08M时,50 - 75%的掺入归因于RNA聚合酶II的活性。在这些条件下,低分子量核RNA的电泳均一的各个组分不会特异性影响RNA聚合酶II的活性。未获得低分子量核RNA参与核不均一RNA合成机制的证据。