TY - JOUR
T1 - A partial-complementary adapter for an improved and simplified ligation-mediated suppression PCR technique
AU - Jeung, Ji Ung
AU - Sung, Ki Cho
AU - Jeong, Sheop Shin
N1 - 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).
Copyright:
Copyright 2008 Elsevier B.V., All rights reserved.
PY - 2005/8/31
Y1 - 2005/8/31
N2 - 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.
AB - 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.
KW - Chromosome walking
KW - Ligation-mediated suppression PCR
KW - Partial-complementary adapter
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U2 - 10.1016/j.jbbm.2005.06.001
DO - 10.1016/j.jbbm.2005.06.001
M3 - Article
C2 - 16005075
AN - SCOPUS:23844556569
SN - 1874-3919
VL - 64
SP - 110
EP - 120
JO - Journal of Proteomics
JF - Journal of Proteomics
IS - 2
ER -