This procedure is easy to use, highly efficient (labeling at 80% of the theoretical incorporation) and generates labeled fragments that are suitable for sequencing.

Gene

A new and simple method has been developed for efficient labeling of the protruding 3' ends of DNA fragments generated by class-II restriction enzymes. This new method utilizes a synthetic oligodeoxynucleotide 5'-GTGCA-3', which is complementary to the protruding 3' end of the fragment and hybridizes with it in such a manner that the end of the restriction fragment will now have a protruding, one-nucleotide (nt)-long 5' end. This then serves as a template to incorporate just one nt at the 3' end of the restriction fragment. This procedure is easy to use, highly efficient (labeling at 80% of the theoretical incorporation) and generates labeled fragments that are suitable for sequencing. We have also improved the nt sequencing procedure of Bencini et al. [Biotechniques 2 (1984) 4-5] by replacing 'A greater than C' reaction with 'G' and 'C' specific reactions and employing butanol precipitation of DNA.

This procedure is easy to use, highly efficient (labeling at 80% of the theoretical incorporation) and generates labeled fragments that are suitable for sequencing.

Radio-labeling of the PstI restriction fragments and improvement in the sequencing procedure.