Universal base analogues and their applications in DNA sequencing technology

被引:18
作者
Liang, Feng [1 ,2 ]
Liu, Ying-Zhu [1 ]
Zhang, Peiming [3 ]
机构
[1] Wuhan Univ Sci & Technol, Coll Chem Engn & Technol, Wuhan 430081, Peoples R China
[2] Wuhan Univ, Key Lab Analyt Chem Biol & Med, Minist Educ, Wuhan 430072, Peoples R China
[3] Arizona State Univ, Biodesign Inst, Tempe, AZ 85287 USA
关键词
SIZE-EXPANDED DNA; PAIRING PROPERTIES; DUPLEX STABILITY; GENETIC HELIX; HYBRIDIZATION PROPERTIES; COMPUTATIONAL ANALYSIS; NUCLEOBASE ANALOGS; NONPOLAR ISOSTERE; OLIGONUCLEOTIDES; NUCLEOSIDE;
D O I
10.1039/c3ra41492b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Universal base analogues are an important class of compounds which pair with all natural bases without discrimination. Since 1990s, a variety of compounds known as universal bases, including hypoxanthine, nitroazoles, isocarbostyril analogues, azole carboxamides and aromatic triazole analogues have been developed and employed in degenerate PCR primers, microarray probes, ligation and triplexes. There are a number of excellent reviews on the applications of universal base analogues in biochemistry and molecular biology, but their use in DNA sequencing has been overlooked, which was the original impetus for the authors to develop universal bases. In this manuscript, the status quo of universal base analogues and their applications in DNA sequencing are discussed, including Sanger sequencing, sequencing by hybridization, sequencing by ligation and sequencing by recognition tunneling. This should be of interest to those working in DNA sequencing technologies, molecular recognition and molecular biology.
引用
收藏
页码:14910 / 14928
页数:19
相关论文
共 181 条
[1]  
AERSCHOT AV, 1995, NUCLEIC ACIDS RES, V23, P4363
[2]   STRINGS OF CONTIGUOUS MODIFIED PENTANUCLEOTIDES WITH INCREASED DNA-BINDING AFFINITY CAN BE USED FOR DNA-SEQUENCING BY PRIMER WALKING [J].
AZHIKINA, T ;
VESELOVSKAYA, S ;
MYASNIKOV, V ;
POTAPOV, V ;
ERMOLAYEVA, O ;
SVERDLOV, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (24) :11460-11462
[3]   Molecular breeding of polymerases for resistance to environmental inhibitors [J].
Baar, Claudia ;
d'Abbadie, Marc ;
Vaisman, Alexandra ;
Arana, Mercedes E. ;
Hofreiter, Michael ;
Woodgate, Roger ;
Kunkel, Thomas A. ;
Holliger, Philipp .
NUCLEIC ACIDS RESEARCH, 2011, 39 (08) :e51
[4]   Novel nucleic acid architectures involving locked nucleic acid (LNA) and pyrene residues: Results from an Indo-Danish collaboration [J].
Babu, BR ;
Raunak ;
Sorensen, MD ;
Hrdlicka, PJ ;
Trikha, S ;
Prasad, AK ;
Parmar, VS ;
Wengel, J .
PURE AND APPLIED CHEMISTRY, 2005, 77 (01) :319-326
[5]   The use of tailed octamer primers for cycle sequencing [J].
Ball, S ;
Reeve, MA ;
Robinson, PS ;
Hill, F ;
Brown, DM ;
Loakes, D .
NUCLEIC ACIDS RESEARCH, 1998, 26 (22) :5225-5227
[6]   Indole in DNA: Comparison of a Nucleosidic with a Non-Nucleosidic DNA Base Substitution [J].
Barbaric, Janez ;
Wanninger-Weiss, Claudia ;
Wagenknecht, Hans-Achim .
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2009, 2009 (03) :364-370
[7]   1-Deoxy-1-(4-fluorophenyl)-β-D-ribofuranose, its hemihydrate, and 1-deoxy-1-(2,4-difluorophenyl)-β-D-ribofuranose:: structural evidence for intermolecular C-H•••F-C interactions [J].
Bats, JW ;
Parsch, J ;
Engels, JW .
ACTA CRYSTALLOGRAPHICA SECTION C-STRUCTURAL CHEMISTRY, 2000, 56 :201-205
[8]   Universal bases for hybridization, replication and chain termination [J].
Berger, M ;
Wu, YQ ;
Ogawa, AK ;
McMinn, DL ;
Schultz, PG ;
Romesberg, FE .
NUCLEIC ACIDS RESEARCH, 2000, 28 (15) :2911-2914
[9]  
Berger M, 2000, ANGEW CHEM INT EDIT, V39, P2940, DOI 10.1002/1521-3773(20000818)39:16<2940::AID-ANIE2940>3.0.CO
[10]  
2-#