Synthesis of high-quality libraries of long (150mer) oligonucleotides by a novel depurination controlled process

被引:219
作者
LeProust, Emily M. [1 ]
Peck, Bill J. [1 ]
Spirin, Konstantin [2 ]
McCuen, Heather Brummel [1 ]
Moore, Bridget [2 ]
Namsaraev, Eugeni [2 ]
Caruthers, Marvin H. [3 ]
机构
[1] Agilent Technol, LSSU Genom, Santa Clara, CA 95051 USA
[2] ParAllele BioSci Inc, San Francisco, CA 94090 USA
[3] Univ Colorado, Dept Chem & Biochem, Boulder, CO 80309 USA
关键词
HELE-SHAW CELL; GENE SYNTHESIS; OLIGODEOXYNUCLEOTIDE SYNTHESIS; MULTIPLEX AMPLIFICATION; SHRNA LIBRARIES; DNA; GENOME; ARRAYS; HYBRIDIZATION; DETRITYLATION;
D O I
10.1093/nar/gkq163
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have achieved the ability to synthesize thousands of unique, long oligonucleotides (150mers) in fmol amounts using parallel synthesis of DNA on microarrays. The sequence accuracy of the oligonucleotides in such large-scale syntheses has been limited by the yields and side reactions of the DNA synthesis process used. While there has been significant demand for libraries of long oligos (150mer and more), the yields in conventional DNA synthesis and the associated side reactions have previously limited the availability of oligonucleotide pools to lengths < 100 nt. Using novel array based depurination assays, we show that the depurination side reaction is the limiting factor for the synthesis of libraries of long oligonucleotides on Agilent Technologies' SurePrint (R) DNA microarray platform. We also demonstrate how depurination can be controlled and reduced by a novel detritylation process to enable the synthesis of high quality, long (150mer) oligonucleotide libraries and we report the characterization of synthesis efficiency for such libraries. Oligonucleotide libraries prepared with this method have changed the economics and availability of several existing applications (e.g. targeted resequencing, preparation of shRNA libraries, site-directed mutagenesis), and have the potential to enable even more novel applications (e.g. high-complexity synthetic biology).
引用
收藏
页码:2522 / 2540
页数:19
相关论文
共 56 条
[1]   HINDERED DIALKYLAMINO NUCLEOSIDE PHOSPHITE REAGENTS IN THE SYNTHESIS OF 2 DNA 51-MERS [J].
ADAMS, SP ;
KAVKA, KS ;
WYKES, EJ ;
HOLDER, SB ;
GALLUPPI, GR .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1983, 105 (03) :661-663
[2]   Targeted and genome-scale strategies reveal gene-body methylation signatures in human cells [J].
Ball, Madeleine P. ;
Li, Jin Billy ;
Gao, Yuan ;
Lee, Je-Hyuk ;
LeProust, Emily M. ;
Park, In-Hyun ;
Xie, Bin ;
Daley, George Q. ;
Church, George M. .
NATURE BIOTECHNOLOGY, 2009, 27 (04) :361-368
[3]  
Bassik MC, 2009, NAT METHODS, V6, P443, DOI [10.1038/NMETH.1330, 10.1038/nmeth.1330]
[4]   ADVANCES IN THE SYNTHESIS OF OLIGONUCLEOTIDES BY THE PHOSPHORAMIDITE APPROACH [J].
BEAUCAGE, SL ;
IYER, RP .
TETRAHEDRON, 1992, 48 (12) :2223-2311
[5]   DEOXYNUCLEOSIDE PHOSPHORAMIDITES - A NEW CLASS OF KEY INTERMEDIATES FOR DEOXYPOLYNUCLEOTIDE SYNTHESIS [J].
BEAUCAGE, SL ;
CARUTHERS, MH .
TETRAHEDRON LETTERS, 1981, 22 (20) :1859-1862
[6]  
Beigelman L, 2000, METHOD ENZYMOL, V317, P39
[7]   Correcting errors in synthetic DNA through consensus shuffling [J].
Binkowski, BF ;
Richmond, KE ;
Kaysen, J ;
Sussman, MR ;
Belshaw, PJ .
NUCLEIC ACIDS RESEARCH, 2005, 33 (06) :1-8
[8]   High-density oligonucleotide arrays [J].
Blanchard, AP ;
Kaiser, RJ ;
Hood, LE .
BIOSENSORS & BIOELECTRONICS, 1996, 11 (6-7) :687-690
[9]   In situ synthesis of oligonucleotide arrays by using surface tension [J].
Butler, JH ;
Cronin, M ;
Anderson, KM ;
Biddison, GM ;
Chatelain, F ;
Cummer, M ;
Davi, DJ ;
Fisher, L ;
Frauendorf, AW ;
Frueh, FW ;
Gjerstad, C ;
Harper, TF ;
Kernahan, SD ;
Long, DQ ;
Pho, M ;
Walker, JA ;
Brennan, TM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2001, 123 (37) :8887-8894
[10]   Protein-mediated error correction for de novo DNA synthesis -: art. no. e162 [J].
Carr, PA ;
Park, JS ;
Lee, YJ ;
Yu, T ;
Zhang, SG ;
Jacobson, JM .
NUCLEIC ACIDS RESEARCH, 2004, 32 (20) :e162