Apte A N, Siebert P D
Clontech Laboratories, Palo Alto, CA 94303-4607.
Biotechniques. 1993 Nov;15(5):890-3.
A new, efficient and simple method based on single-stranded anchor ligation has been developed that allows for the generation of an anchor-ligated library from which the 5' ends in many mRNAs can be cloned. Random hexamers are used to prime poly A+ RNA for the first strand synthesis of a cDNA library, and a modified single-stranded anchor is then ligated to the 3' end of the cDNA using T4 RNA ligase. The library can then be used to amplify the 5' end of any mRNA expressed in the tissue. The efficiency and utility of this method has been demonstrated by amplification of three human genes: transferrin receptor, tissue-type plasminogen activator and beta actin.
一种基于单链锚定连接的新型高效简便方法已被开发出来,该方法能够从锚定连接文库中克隆许多mRNA的5'端。随机六聚体用于引发聚腺苷酸加尾RNA以合成cDNA文库的第一链,然后使用T4 RNA连接酶将修饰的单链锚定连接到cDNA的3'端。该文库随后可用于扩增组织中表达的任何mRNA的5'端。通过扩增三种人类基因:转铁蛋白受体、组织型纤溶酶原激活剂和β-肌动蛋白,证明了该方法的效率和实用性。