Thompson E W, Lane B G
J Biol Chem. 1980 Jun 25;255(12):5965-70.
Dry wheat embryos were allowed to imbibe water in the presence or absence of an inhibitor of mRNA synthesis (alpha-amanitin). At each of a series of times after the onset of imbibition, newly synthesized polypeptides were labeled, isolated, and compared with those made by cell-free translation of RNA prepared from the same embryos. In the absence of alpha-amanitin, characteristic time-dependent changes in the relative proportions of many polypeptides in the electrophoretic distributions of proteins synthesized in imbibing wheat embryos could be correlated with parallel changes in the cell-free translational capacity of bulk mRNA from the same embryos. These changes were virtually eliminated when alpha-amanitin was present in the imbibing medium. The findings are consistent with the possibility that transcription of new mRNA, which begins with the onset of imbibition, is responsible for change in the electrophoretic distributions of nascent polypeptides between 40 min and 5 h postimbibition of dry wheat embryos (Cuming, A. C. & Lane, B. G (1979) Eur. J. Biochem. 99, 217-224). Allied with the principal investigation, a useful modification has been developed in order to obtain an improved field of resolution (encompassing a range of Mr values between less than 5 X 10(5) and greater than 200 X 10(3), without using a gradient in sodium dodecyl sulfate/polyacrylamide gel.
将干燥的小麦胚在有或无mRNA合成抑制剂(α-鹅膏蕈碱)的情况下吸水。在吸水开始后的一系列时间点,对新合成的多肽进行标记、分离,并与由相同胚制备的RNA进行无细胞翻译所产生的多肽进行比较。在没有α-鹅膏蕈碱的情况下,吸水的小麦胚中合成的蛋白质电泳分布中许多多肽的相对比例随时间的特征性变化,可与来自相同胚的大量mRNA的无细胞翻译能力的平行变化相关联。当吸水培养基中存在α-鹅膏蕈碱时,这些变化几乎消失。这些发现与以下可能性一致,即从吸水开始的新mRNA转录,是导致干燥小麦胚吸水后40分钟至5小时之间新生多肽电泳分布变化的原因(卡明,A.C.和莱恩,B.G.(1979年)《欧洲生物化学杂志》99卷,217 - 224页)。与主要研究相关,为了获得更好的分辨率范围(涵盖小于5×10⁵至大于200×10³的一系列Mr值),在不使用十二烷基硫酸钠/聚丙烯酰胺凝胶梯度的情况下,开发了一种有用的改进方法。