Malt R A
J Exp Med. 1966 Oct 1;124(4):679-88. doi: 10.1084/jem.124.4.679.
Much of the RNA in mouse kidneys is not recovered when they are extracted with phenol-SDS at 60 degrees C. Better recovery is achieved by extracting in hypertonic buffer with phenol-SDS, chloroform, and isoamyl alcohol after treatment with DNase. 1. Among the polydisperse RNA in the renal nuclei are small amounts of 45S RNA and large amounts of 32S RNA; the latter first appear when 18S RNA is detectable in the cytoplasm 10 min after administration of undine-H(3). 2. In the cytoplasm rapidly labeled 18S RNA is transported as part of a 45S particle to which mRNA is attached. 3. Compared to HeLa cells in culture, normal mouse kidney is poor in the polydisperse nuclear precursors of rRNA and rich in the cytoplasmic polydisperse RNA that sediments like mRNA.
当用苯酚 - SDS在60摄氏度提取小鼠肾脏中的RNA时,大部分RNA无法回收。在用DNase处理后,通过在含有苯酚 - SDS、氯仿和异戊醇的高渗缓冲液中提取,可以实现更好的回收。1. 在肾细胞核中的多分散RNA中,有少量的45S RNA和大量的32S RNA;后者在给予尿苷 - H(3) 10分钟后,当细胞质中可检测到18S RNA时首次出现。2. 在细胞质中,快速标记的18S RNA作为45S颗粒的一部分被转运,mRNA附着于该颗粒。3. 与培养的HeLa细胞相比,正常小鼠肾脏中rRNA的多分散核前体较少,而富含像mRNA一样沉降的细胞质多分散RNA。