Miller A O, Dhont E, Miller-Faures A, Aguilera A
Arch Int Physiol Biochim. 1976 Feb;84(1):15-33. doi: 10.3109/13813457609072343.
Together with the elution pattern of pure messenger RNA molecules of various origin, the labelling kinetics of rapidly labelled heterogeneously sedimenting RNA (HSRNA) extracted from polysomes of HeLa cells have been studied by chromatogrphy on columns made of methylated bovine serum albumin adsorbed on kieselguhr. HSRNA is eluted within three peaks-IP, Q2P and TDP-following in that order the increase of NaC1 concentration in the eluting buffer. Besides peak TDP which results from an experimental artefact, our data suggest that the appearance of peaks IP and Q2P reflects the absence and presence respectively of polyadenylic acid stretches in these molecules. Within peak Q2P, the critical factor affecting the order of elution is the size of the polyadenylic acid stretch.
结合各种来源的纯信使RNA分子的洗脱模式,通过在吸附于硅藻土的甲基化牛血清白蛋白制成的柱上进行色谱分析,研究了从HeLa细胞多核糖体中提取的快速标记的不均一沉降RNA(HSRNA)的标记动力学。HSRNA在三个峰——IP、Q2P和TDP中被洗脱,洗脱缓冲液中NaCl浓度按此顺序增加。除了由实验假象导致的TDP峰外,我们的数据表明,IP峰和Q2P峰的出现分别反映了这些分子中聚腺苷酸链的缺失和存在。在Q2P峰内,影响洗脱顺序的关键因素是聚腺苷酸链的长度。