Gurdon J B, Melton D A, De Robertis E M
Ciba Found Symp. 1979(66):63-80. doi: 10.1002/9780470720486.ch5.
The combination of DNA cloning in bacterial plasmids and DNA injection into frog oocyte nuclei permits a novel type of genetic analysis in which the function of defined sequences of DNA may be more readily and precisely investigated than before. Purified segments of chromosomal DNA containing 5S genes of Xenopus have been injected into the nuclei of Xenopus oocytes and the products of these genes recognized as labelled 5S RNA. Since short linear molecules of DNA are degraded in oocytes, the function of particular regions of DNA near a 5S gene is best determined by excising these regions and joining them to other kinds of DNA. This is achieved most simply by inserting regions of 5S DNA into a plasmid. Our results with alpha-amanitin show that the activity of a 5S DNA promoter inserted into a plasmid can be detected independently of the plasmid's own promoters, using DNA injection into oocytes. The observation that plasmids containing variant 5S genes result in the synthesis of abnormal 5S RNA molecules illustrates the possibility of mutanting recombinant plasmids and then testing the biological effect of these mutations by DNA injection.
细菌质粒中的DNA克隆与向蛙卵母细胞核中注射DNA相结合,使得一种新型的遗传分析成为可能,在这种分析中,与以往相比,可以更容易、更精确地研究特定DNA序列的功能。含有非洲爪蟾5S基因的染色体DNA纯化片段已被注射到非洲爪蟾卵母细胞核中,这些基因的产物被识别为标记的5S RNA。由于DNA短线性分子在卵母细胞中会被降解,因此5S基因附近特定DNA区域的功能最好通过切除这些区域并将它们连接到其他类型的DNA上来确定。最简单的方法是将5S DNA区域插入质粒。我们用α-鹅膏蕈碱得到的结果表明,将注射到卵母细胞中的DNA用于检测时,插入质粒中的5S DNA启动子的活性可以独立于质粒自身的启动子被检测到。含有变异5S基因的质粒会导致异常5S RNA分子的合成,这一观察结果说明了突变重组质粒,然后通过DNA注射测试这些突变的生物学效应的可能性。