Boedtker H, Frischauf A M, Lehrach H
Biochemistry. 1976 Nov 2;15(22):4765-70. doi: 10.1021/bi00667a003.
Procollagen messenger ribonucleic acid (mRNA) was isolated from the calvaria of 15-day-old chick embryos by chromatographing total RNA over oligo(dT)-cellulose two times, and then fractionating the twice-bound RNA on 85% Me2SO/0-20% sucrose gradients. When analyzed on 99% formamide gels, the 27-30S fraction had three sharp fluorescent bands, one corresponding to 27S ribosomal RNA (rRNA), the others having mobilities lower than 27S corresponding to molecular weights of 1 700 000 and 1 800 000. In wheat-germ, cell-free extracts, the 27-30S fraction directed the synthesis of two prominent collagenase sensitive polypeptides with mobilities corresponding to the calvaria pro-alpha chain markers. Twelve percent of this [3H]proline-labeled, wheat-germ product could be hydroxylated with prolyl hydroxylase.
通过将总RNA在寡聚(dT)-纤维素上进行两次层析,然后在85%二甲基亚砜/0-20%蔗糖梯度上对两次结合的RNA进行分级分离,从15日龄鸡胚的颅骨中分离出前胶原信使核糖核酸(mRNA)。在99%甲酰胺凝胶上进行分析时,27-30S级分有三条清晰的荧光带,一条对应于27S核糖体RNA(rRNA),其他条带的迁移率低于27S,对应分子量为1700000和1800000。在小麦胚芽无细胞提取物中,27-30S级分指导合成了两种突出的胶原酶敏感多肽,其迁移率与颅骨前α链标记物相对应。这种用[3H]脯氨酸标记的小麦胚芽产物的12%可以被脯氨酰羟化酶羟化。