Jang Y K, Jin Y H, Kim M J, Seong R H, Hong S H, Park S D
Department of Molecular Biology, Seoul National University, Republic of Korea.
Biochem Mol Biol Int. 1995 Oct;37(2):339-44.
A simple and efficient procedure was described for the isolation of total RNA from the fission yeast Schizosaccharomyces pombe. The present study demonstrated that the quality and the quantity of S. pombe RNA were increased by substituting phenol/chloroform mixture for phenol as a deproteinizing agent in the first vortexing step and using an ice bath instead of a dry ice-ethanol bath in the freezing step. Additionally, this protocol had the advantage of extracting total RNA without any degradation of S. pombe cells. Furthermore, the high amounts and quality of RNA extracted by this modified procedure enabled us to perform some experiments such as Northern blot, S1 mapping, primer extension, and reverse transcriptase reaction-polymerase chain reaction (RT-PCR) without further RNA purification. We suggest that this procedure is very useful to analyse primary structures and steady-state levels of RNA from S. pombe.
描述了一种从裂殖酵母粟酒裂殖酵母中分离总RNA的简单高效方法。本研究表明,通过在第一步涡旋步骤中用苯酚/氯仿混合物替代苯酚作为脱蛋白剂,并在冷冻步骤中使用冰浴而非干冰-乙醇浴,粟酒裂殖酵母RNA的质量和数量得以提高。此外,该方案具有在不破坏粟酒裂殖酵母细胞的情况下提取总RNA的优点。此外,通过这种改进方法提取的大量高质量RNA使我们能够进行一些实验,如Northern印迹、S1作图、引物延伸和逆转录酶反应-聚合酶链反应(RT-PCR),而无需进一步纯化RNA。我们认为该方法对于分析粟酒裂殖酵母RNA的一级结构和稳态水平非常有用。