Sargent T D, Dawid I B
Science. 1983 Oct 14;222(4620):135-9. doi: 10.1126/science.6688681.
A modified cloning method designed to produce differential complementary DNA libraries permits the isolation of sequences that are present in the RNA population of any developmental stage or tissue, but are not present or are much less abundant in another stage or tissue. Selective complementary DNA cloning is especially useful when the differentially expressed RNA's are of low to moderate abundance in the cells in which they occur. A class of cytoplasmic polyadenylated RNA's differentially expressed in gastrula embryos of Xenopus laevis (DG RNA's) has been isolated. These DG RNA's occur very rarely or not at all in unfertilized eggs and blastulae, accumulate as the result of transcription before and during gastrulation, and, with some exceptions, decline in abundance as development proceeds. Many of these RNA molecules appear to be translated at the gastrula stage. Thus, DG RNA's may encode proteins that are important in the process of gastrulation.
一种旨在构建差异互补DNA文库的改良克隆方法,能够分离出存在于任何发育阶段或组织的RNA群体中,但在其他阶段或组织中不存在或丰度低得多的序列。当差异表达的RNA在其出现的细胞中丰度较低至中等时,选择性互补DNA克隆特别有用。已分离出一类在非洲爪蟾原肠胚中差异表达的细胞质聚腺苷酸化RNA(DG RNA)。这些DG RNA在未受精卵和囊胚中很少出现或根本不出现,在原肠胚形成之前和期间由于转录而积累,并且,除了一些例外,随着发育的进行丰度下降。这些RNA分子中的许多似乎在原肠胚阶段被翻译。因此,DG RNA可能编码在原肠胚形成过程中重要的蛋白质。