DNA sequencing by denaturation: Principle and thermodynamic simulations

被引:13
作者
Chen, Ying-Ja [1 ]
Huang, Xiaohua [1 ]
机构
[1] Univ Calif San Diego, Dept Bioengn, La Jolla, CA 92093 USA
基金
美国国家科学基金会;
关键词
DNA sequencing; Melting curve analysis; Sequencing by denaturation; Nearest-neighbor model; Thermodynamics; Melting temperature; Denaturation; Hybridization; REVERSIBLE TERMINATORS; DUPLEX STABILITY; HYBRIDIZATION; GENOME; OLIGONUCLEOTIDE; GENERATION; TECHNOLOGIES; POLYMERASE; PREDICTION; PARAMETERS;
D O I
10.1016/j.ab.2008.09.048
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We describe a new DNA sequencing method called sequencing by denaturation (SBD). A Sanger dideoxy sequencing reaction is performed on the templates on a solid surface to generate a ladder of DNA fragments randomly terminated by fluorescently labeled dideoxyribonucleotides. The labeled DNA fragments are sequentially denatured from the templates and the process is monitored by measuring the change in fluorescence intensities from the surface. By analyzing the denaturation profiles, the base sequence of the template can be determined. Using thermodynamic principles, we simulated the denaturation profiles of a series of oligonucleotides ranging from 12 to 32 bases and developed a base-calling algorithm to decode the sequences. These simulations demonstrate that DNA molecules up to 20 bases can be sequenced by SBD. Experimental measurements of the melting profiles of DNA fragments in solution confirm that DNA sequences can be determined by SBD. The potential limitations and advantages of SBD are discussed. With SBD, millions of sequencing reactions can be performed on a small area on a surface in parallel with a very small amount of sequencing reagents. Therefore, DNA sequencing by SBD could potentially result in a significant increase in speed and reduction in cost in large-scale genome resequencing. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:170 / 179
页数:10
相关论文
共 45 条
[1]  
Anderson M.L. M., 1999, Nucleic Acid Hybridization
[2]   Magnetic assembly of high-density DNA arrays for genomic analyses [J].
Barbee, Kristopher D. ;
Huang, Xiaohua .
ANALYTICAL CHEMISTRY, 2008, 80 (06) :2149-2154
[3]   Sequencing single molecules of DNA [J].
Bayley, Hagan .
CURRENT OPINION IN CHEMICAL BIOLOGY, 2006, 10 (06) :628-637
[4]   The LightTyper™:: High-throughput genotyping using fluorescent melting curve analysis [J].
Bennett, CD ;
Campbell, MN ;
Cook, CJ ;
Eyre, DJ ;
Nay, LM ;
Nielsen, DR ;
Rasmussen, RP ;
Bernard, PS .
BIOTECHNIQUES, 2003, 34 (06) :1288-+
[5]  
Bloomfield V. A., 2000, Nucleic Acids: Structures, Properties, and Functions
[6]   STABILITY OF RIBONUCLEIC-ACID DOUBLE-STRANDED HELICES [J].
BORER, PN ;
DENGLER, B ;
TINOCO, I ;
UHLENBECK, OC .
JOURNAL OF MOLECULAR BIOLOGY, 1974, 86 (04) :843-853
[7]   PREDICTING DNA DUPLEX STABILITY FROM THE BASE SEQUENCE [J].
BRESLAUER, KJ ;
FRANK, R ;
BLOCKER, H ;
MARKY, LA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (11) :3746-3750
[8]   Accessing genetic information with high-density DNA arrays [J].
Chee, M ;
Yang, R ;
Hubbell, E ;
Berno, A ;
Huang, XC ;
Stern, D ;
Winkler, J ;
Lockhart, DJ ;
Morris, MS ;
Fodor, SPA .
SCIENCE, 1996, 274 (5287) :610-614
[9]   Stem cell transcriptome profiling via massive-scale mRNA sequencing [J].
Cloonan, Nicole ;
Forrest, Alistair R. R. ;
Kolle, Gabriel ;
Gardiner, Brooke B. A. ;
Faulkner, Geoffrey J. ;
Brown, Mellissa K. ;
Taylor, Darrin F. ;
Steptoe, Anita L. ;
Wani, Shivangi ;
Bethel, Graeme ;
Robertson, Alan J. ;
Perkins, Andrew C. ;
Bruce, Stephen J. ;
Lee, Clarence C. ;
Ranade, Swati S. ;
Peckham, Heather E. ;
Manning, Jonathan M. ;
McKernan, Kevin J. ;
Grimmond, Sean M. .
NATURE METHODS, 2008, 5 (07) :613-619
[10]   A vision for the future of genomics research [J].
Collins, FS ;
Green, ED ;
Guttmacher, AE ;
Guyer, MS .
NATURE, 2003, 422 (6934) :835-847