Gebauer H U, Seitz U, Seitz U
Z Naturforsch C Biosci. 1975 Mar-Apr;30(2):213-8. doi: 10.1515/znc-1975-3-411.
In freely suspended cells of parsley (Petroselinum crispum) protein synthesis is inhibited nearly totally by 5 mug/ml cycloheximide within 10 min. This very low dose has a slight effect on the rRNA synthesis too. During an incubation period of 60 min with [32P] orthophosphate in the presence of the inhibitor (5 mug/ml) at least 65-70% mature rRNA are synthesized compared with the control. After 120 min the synthesis is progressively reduced to 60-65%, and after 240 min to 30-40%. Cycloheximide causes a delay of the prn addition to the 2.3 X 10(6) daltons RNA, normally detectable in pulse experiments, two further precursor molecules do emerge which undernormal circumstances apparently are shortlived. Their molecular weights are 2.0 X 10(6) and 0.9 X 10(6) daltons. The pulse-chase technique and cell fractionation into nuclear and ribosomal parts enables us to demonstrate a rapid transfer of labelled 18S and 25S RNA during a 15 min chase treatment to the mature cytoplasmic ribosomes. Under these conditions no differential transport of the two components takes place. The cells possess a pool of proteins. Therefore the formation of RNP-particles or ribosomes respectively and the transport from the nucleus to the cytoplasm are indipendent from protein synthesis for some time.
在自由悬浮的欧芹(Petroselinum crispum)细胞中,蛋白质合成在10分钟内几乎完全被5微克/毫升的环己酰亚胺抑制。这个极低的剂量对rRNA合成也有轻微影响。在存在抑制剂(5微克/毫升)的情况下,用[32P]正磷酸盐孵育60分钟期间,与对照相比,至少65 - 70%的成熟rRNA被合成。120分钟后,合成逐渐减少到60 - 65%,240分钟后减少到30 - 40%。环己酰亚胺导致向2.3×10(6)道尔顿RNA添加prn延迟,在脉冲实验中通常可以检测到,另外出现了两个前体分子,在正常情况下它们显然寿命很短。它们的分子量分别为2.0×10(6)和0.9×10(6)道尔顿。脉冲追踪技术以及将细胞分离成细胞核和核糖体部分,使我们能够证明在15分钟的追踪处理过程中,标记的18S和25S RNA快速转移到成熟的细胞质核糖体中。在这些条件下,这两种成分没有差异运输。细胞拥有蛋白质库。因此,RNP颗粒或核糖体的形成以及从细胞核到细胞质的运输在一段时间内与蛋白质合成无关。