Schulz-Harder B, Thüroff E
FEBS Lett. 1984 Mar 12;168(1):61-4. doi: 10.1016/0014-5793(84)80206-9.
We have developed an efficient transcription system in isolated yeast nuclei. If MnCl2 is substituted by CdCl2, degradation of newly synthesized RNA is markedly reduced. This effect is due to the inhibition of nuclear ribonuclease activity, since microsomal ribonuclease activity is less affected by the cation. The extent to which the addition of CdCl2 to the in vitro transcription assay inhibits ribonuclease activity is demonstrated by the measurements of the size of newly synthesized RNA. Efficient RNA synthesis in this system is not affected up to a concentration of 0.1 M CdCl2.
我们在分离的酵母细胞核中开发了一种高效的转录系统。如果用氯化镉替代氯化锰,新合成RNA的降解会显著减少。这种效应是由于核糖核酸酶活性受到抑制,因为微粒体核糖核酸酶活性受阳离子的影响较小。通过测量新合成RNA的大小,证明了在体外转录试验中添加氯化镉对核糖核酸酶活性的抑制程度。在该系统中,高达0.1 M的氯化镉浓度都不会影响高效的RNA合成。