Duby A, Jacobs K A, Celeste A
The University of Texas Health Science Center at Dallas, Dallas, Texas, USA.
Curr Protoc Mol Biol. 2001 May;Chapter 6:Unit6.4. doi: 10.1002/0471142727.mb0604s09.
The protocols in this unit describe procedures for using mixtures of 32P-labeled oligonucleotides to screen recombinant DNA clones bound to nitrocellulose filters. A partial amino acid sequence of a protein is used to predict the nucleotide sequence of the gene that would encode it. A mixture of oligonucleotides is chosen that includes all possible nucleotide sequences encoding that amino acid sequence. This mixture of oligonucleotides is then used to screen a recombinant DNA library for the corresponding clones. In some cases however, the exact nucleotide sequence of a desired clone is known and it is possible to use a unique oligonucleotide as a probe.
本单元中的方案描述了使用32P标记的寡核苷酸混合物筛选与硝酸纤维素滤膜结合的重组DNA克隆的程序。蛋白质的部分氨基酸序列用于预测编码该蛋白质的基因的核苷酸序列。选择包含编码该氨基酸序列的所有可能核苷酸序列的寡核苷酸混合物。然后使用该寡核苷酸混合物筛选重组DNA文库以寻找相应的克隆。然而,在某些情况下,所需克隆的确切核苷酸序列是已知的,并且可以使用独特的寡核苷酸作为探针。