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Eur J Biochem. 1984 Dec 3;145(2):351-7. doi: 10.1111/j.1432-1033.1984.tb08561.x.
The early-methionine-labelled (Em) polypeptide is the most abundant single polypeptide found in the cytosolic fraction (30 000 X g supernatant) of dry wheat embryos. Synthesis of this polypeptide is readily detectable during the earliest stages (0-3 h) of wheat embryo germination, by labelling with [35S]methionine. Thereafter, synthesis of the Em polypeptide declines rapidly. A DNA sequence encoding a portion of this polypeptide has been isolated by the molecular cloning of DNA complementary to the messenger RNA from dry wheat embryos. The identity of this cloned sequence has been confirmed by hybrid-selected translation of the Em messenger, the product being analysed by one- and two-dimensional polyacrylamide gel electrophoresis, and by analysis of its partial proteolytic digestion products. Gel blot hybridisation of RNA isolated from embryos at successive stages of germination with this cloned DNA sequence confirms that the decline in the synthesis of the Em polypeptide, detected by labelling in vivo, is a consequence of the degradation of its corresponding messenger RNA.
早期甲硫氨酸标记(Em)多肽是在干燥小麦胚的胞质部分(30000×g上清液)中发现的最丰富的单一多肽。在小麦胚萌发的最早阶段(0 - 3小时),通过用[35S]甲硫氨酸标记,很容易检测到这种多肽的合成。此后,Em多肽的合成迅速下降。通过对来自干燥小麦胚的信使RNA的互补DNA进行分子克隆,分离出了编码该多肽一部分的DNA序列。通过对Em信使进行杂交选择翻译(产物经一维和二维聚丙烯酰胺凝胶电泳分析)以及对其部分蛋白水解消化产物进行分析,证实了该克隆序列的身份。用该克隆DNA序列与从萌发连续阶段的胚中分离的RNA进行凝胶印迹杂交,证实了通过体内标记检测到的Em多肽合成下降是其相应信使RNA降解的结果。