Abstract
Ligation-mediated suppression PCR (LMS-PCR) is a powerful tool for walking in unknown genomic DNA regions from known adjacent sequences. This approach has made it feasible to obtain promoter sequences and to enable researchers to identify full-length gene sequences or isoforms of multigene families. However, the advantages of LMS-PCR can be obviated by the presence of incomplete base modifications on the suppression adapters. We propose here that a 'partial-complementary adapter' is a more reliable suppression adapter, demanding only 5′-end phosphorylation. We also describe a simplified procedure for the easier preparation of PCR templates with very small quantities of DNA and a fast and direct characterization of the suppression-PCR products. A set of practical guidelines is proposed for pre-checking the efficiency of the adapter modification using two model systems: bacteriophage λ (λ) and Arabidopsis.
Original language | English |
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Pages (from-to) | 110-120 |
Number of pages | 11 |
Journal | Journal of Biochemical and Biophysical Methods |
Volume | 64 |
Issue number | 2 |
DOIs | |
Publication status | Published - 2005 Aug 31 |
Bibliographical note
Funding Information:This project was funded by the Post-doctoral Fellowship Program of the Basic Research Promotion Fund from the Korea Research Foundation (to S.K.C.; M01-2004-000-10035-0).
Keywords
- Chromosome walking
- Ligation-mediated suppression PCR
- Partial-complementary adapter
ASJC Scopus subject areas
- Biophysics
- Biochemistry