Ligation-based synthesis of oligonucleotides with block structure

被引:8
作者
Borodina, TA [1 ]
Lehrach, H [1 ]
Soldatov, AV [1 ]
机构
[1] Max Planck Inst Mol Genet, D-14195 Berlin, Germany
关键词
oligonucleotides; primers; padlock probe; block structure;
D O I
10.1016/S0003-2697(03)00250-1
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We describe here a method for the synthesis of oligonucleotides with block structure (padlock probes, primers for multiplex polymerase chain reaction (PCR), and ligation-independent cloning), based on the ligation of presynthesized parts by T4 DNA ligase. The advantages of this approach are: (i) suitability of the technology for any producer-from synthesis company to laboratory, (ii) high quality and adjustable scale of synthesis, and (iii) possibility of including any modified bases inexpensively in the common part of the oligonucleotide. Clear difference of sizes of products and substrates makes the synthesis amenable to automation. For large series of padlock probes, the price per one primer approaches the price of the locus-specific parts. We demonstrate the application of this method to two different tasks: preparative-scale production of padlock probes and small-scale synthesis of PCR primers. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:309 / 313
页数:5
相关论文
共 15 条
[1]   PCR-generated padlock probes detect single nucleotide variation in genomic DNA [J].
Antson, D. -O. ;
Isaksson, A. ;
Landegren, U. ;
Nilsson, M. .
NUCLEIC ACIDS RESEARCH, 2000, 28 (12) :58
[2]   Relating structure to function in phi 29 DNA polymerase [J].
Blanco, L ;
Salas, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (15) :8509-8512
[3]   Use of T7 gene 6 exonuclease and phosphorothioated primers for the manipulation of HIV-1 infectious clones [J].
da Costa, LJ ;
Tanuri, A .
JOURNAL OF VIROLOGICAL METHODS, 1998, 72 (01) :117-121
[4]   High throughput methods for gene cloning and expression [J].
Dieckman, L ;
Gu, MY ;
Stols, L ;
Donnelly, MI ;
Collart, FR .
PROTEIN EXPRESSION AND PURIFICATION, 2002, 25 (01) :1-7
[5]   Universal DNA array detection of small insertions and deletions in BRCA1 and BRCA2 [J].
Favis, R ;
Day, JP ;
Gerry, NP ;
Phelan, C ;
Narod, S ;
Barany, F .
NATURE BIOTECHNOLOGY, 2000, 18 (05) :561-564
[6]  
KALUZ S, 1995, BIOTECHNIQUES, V19, P182
[7]   Large-scale discovery and genotyping of single-nucleotide polymorphisms in the mouse [J].
Lindblad-Toh, K ;
Winchester, E ;
Daly, MJ ;
Wang, DG ;
Hirschhorn, JN ;
Laviolette, JP ;
Ardlie, K ;
Reich, DE ;
Robinson, E ;
Sklar, P ;
Shah, N ;
Thomas, D ;
Fan, JB ;
Gingeras, T ;
Warrington, J ;
Patil, N ;
Hudson, TJ ;
Lander, ES .
NATURE GENETICS, 2000, 24 (04) :381-386
[8]   Mutation detection and single-molecule counting using isothermal rolling-circle amplification [J].
Lizardi, PM ;
Huang, XH ;
Zhu, ZR ;
Bray-Ward, P ;
Thomas, DC ;
Ward, DC .
NATURE GENETICS, 1998, 19 (03) :225-232
[9]   Evaluation of single nucleotide polymorphism typing with invader on PCR amplicons and its automation [J].
Mein, CA ;
Barratt, BJ ;
Dunn, MG ;
Siegmund, T ;
Smith, AN ;
Esposito, L ;
Nutland, S ;
Stevens, HE ;
Wilson, AJ ;
Phillips, MS ;
Jarvis, N ;
Law, S ;
de Arruda, M ;
Todd, JA .
GENOME RESEARCH, 2000, 10 (03) :330-343
[10]   Synthesis and application of circularizable ligation probes [J].
Myer, SE ;
Day, DJ .
BIOTECHNIQUES, 2001, 30 (03) :584-+