Lönn U, Edström J E
J Cell Biol. 1976 Sep;70(3):573-80. doi: 10.1083/jcb.70.3.573.
Analysis in insect (Chironomus tentans) salivary gland cells of labeled RNA as a function of time after precursor injection and its distance to the nuclear membrane, cytoplasmic zone analysis, could previously be used to demonstrate the presence of short-lasting gradients in newly labeled ribosomal RNA. Since the gradients were sensitive to puromycin, they are likely to be a result of diffusion restriction due to an engagement of the subunits into polysomes. In the present paper the possibility was explored of recording gradients that were caused by labeled subunits in puromycin-resistant associations, which, in all probability, involve the endoplasmic reticulum. It was found that labeled 28 S and 5 S RNA but not 18 S RNA were present in radioactivity gradients lasting for at least 2 days but less than 6 days. The gradients also remained during inhibition of RNA synthesis by actinomycin, and they were completely resistant to puromycin whether given in vivo or in vitro. The semipermanent gradients formed fhere offer a unique parameter for the in vivo study of conditions for formation and maintenance of heavy subunits in puromycin-resistant bonds. An explanation for these and previous results is that the light subunit, although restricted in movement by engagement to polysomes, is nevertheless free to exchange and spread between rounds of translation, whereas at least part of the heavy subunit population is bound to the endoplasmic reticulum and less free to spread. These results offer a good in vivo correlate to previous results on in vitro exchangeability of subunits.
分析注射前体后不同时间点标记RNA在昆虫(摇蚊)唾液腺细胞中的情况及其与核膜的距离(细胞质区域分析),此前可用于证明新标记的核糖体RNA中存在短期梯度。由于这些梯度对嘌呤霉素敏感,它们可能是由于亚基参与多核糖体而导致扩散受限的结果。在本文中,探讨了记录由嘌呤霉素抗性结合中的标记亚基引起的梯度的可能性,这种结合很可能涉及内质网。结果发现,标记的28S和5S RNA存在放射性梯度中,持续至少2天但少于6天,而18S RNA则不存在。在放线菌素抑制RNA合成期间,这些梯度仍然存在,并且无论在体内还是体外给予嘌呤霉素,它们都完全抗性。在此形成的半永久性梯度为体内研究嘌呤霉素抗性键中重亚基形成和维持的条件提供了一个独特的参数。对这些结果和先前结果的一种解释是,轻亚基虽然因参与多核糖体而移动受限,但在翻译轮次之间仍可自由交换和扩散,而至少部分重亚基群体与内质网结合,扩散较不自由。这些结果为先前关于亚基体外可交换性的结果提供了良好的体内相关性。