Access the full text.
Sign up today, get DeepDyve free for 14 days.
AP Lewis, MJ Sims, DR Gewert, TC Peakman, H Spence, JS Crowe (1994)
Taq DNA polymerase extension of internal primers blocks polymerase chain reactions allowing differential amplification of molecules with identical 5? and 3? endsNucleic Acids Res, 22
JM Rouillard, W Lee, G Truan, X Gao, X Zhou, E Gulari (2004)
Gene2Oligo: oligonucleotide design for in vitro gene synthesisNucleic Acids Res, 32
R Chakrabarti, CE Schutt (2001)
The enhancement of PCR amplification by low molecular weight amidesNucleic Acids Res, 29
O Shalem, E Sharon, S Lubliner, I Regev, M Lotan-Pompan, Z Yakhini, E Segal (2015)
Systematic dissection of the sequence determinants of gene 3? end mediated expression controlPLoS Genet, 11
LJ Kahl, D Endy (2013)
A�survey�of�enabling�technologies�in�synthetic biologyJ Biol Eng, 7
HO Smith, CA Hutchison, C Pfannkoch, JC Venter (2003)
Generating a synthetic genome by whole genome assembly: phiX174 bacteriophage from synthetic oligonucleotidesProc Natl Acad Sci USA, 100
DG Gibson, L Young, RY Chuang, JC Venter, CA Hutchison, HO Smith (2009)
Enzymatic assembly of DNA molecules up to several hundred kilobasesNat Methods, 6
K Tsuge, Y Sato, Y Kobayashi, M Gondo, M Hasebe, T Togashi, M Tomita, M Itaya (2015)
Method of preparing an equimolar DNA mixture for one-step DNA assembly of over 50 fragmentsSci Rep, 5
N Agier, OM Romano, F Touzain, M Cosentino Lagomarsino, G Fischer (2013)
The spatiotemporal program of replication in the genome of Lachancea kluyveriGenome Biol Evol, 5
YY Guo, ZY Shi, XZ Fu, JC Chen, Q Wu, GQ Chen (2015)
A strategy for enhanced circular DNA construction efficiency based on DNA cyclization after microbial transformationMicrob Cell Fact, 14
DG Gibson, GA Benders, CA Pfannkoch (2008)
Complete chemical synthesis, assembly, and cloning of a Mycoplasma genitalium genomeScience, 319
D Bang, GM Church (2008)
Gene synthesis by circular assembly amplificationNat Methods, 5
S Wang, Y Luo, X Yi (2007)
A highly efficient and highly reliable protocol for transformation of Escherichia coli by electroporationJ Rapid Methods Autom Microbiol, 15
RG Michael, J Sambrook (2012)
Molecular cloning: a laboratory manual
XZ Su, Y Wu, CD Sifri, TE Wellems (1996)
Reduced extension temperatures required for PCR amplification of extremely A�+�T-rich DNANucleic Acids Res, 24
TL Roth, L Milenkovic, MP Scott (2014)
A rapid and simple method for DNA engineering using cycled ligation assemblyPLoS ONE, 9
B Bartholdy, R Mukhopadhyay, J Lajugie, MI Aladjem, EE Bouhassira (2015)
Allele-specific analysis of DNA replication origins in mammalian cellsNat Commun, 6
R Arratia, D Martin, G Reinert, MS Waterman (1996)
Poisson process approximation for sequence repeats, and sequencing by hybridizationJ Comput Biol, 3
UB Gyllensten, HA Erlich (1988)
Generation of single-stranded DNA by the polymerase chain reaction and its application to direct sequencing of the HLA-DQA locusProc Natl Acad Sci USA, 85
R Sorek, Y Zhu, CJ Creevey, MP Francino, P Bork, EM Rubin (2007)
Genome-wide experimental determination of barriers to horizontal gene transferScience, 318
DG Gibson, HO Smith, CA Hutchison, JC Venter, C Merryman (2010)
Chemical synthesis of the mouse mitochondrial genomeNat Methods, 7
R Arratia, L Goldstein, L Gordon (1990)
Poisson approximation and the Chen?Stein methodStat Sci, 5
HY Ye, MC Huang, MH Li, JY Ying (2009)
Experimental analysis of gene assembly with TopDown one-step real-time gene synthesisNucleic Acids Res, 37
JP Torella, CR Boehm, F Lienert, JH Chen, JC Way, PA Silver (2014)
Rapid construction of insulated genetic circuits via synthetic sequence-guided isothermal assemblyNucleic Acids Res, 42
Extraordinary adenine/thymine rich DNA has a low complexity resulting in the occurrence of many short repetitive sequences or longer imperfect repeats, consequently hindering the gene synthesis process. This report describes the rapid synthesis of a DNA fragment with guanine/cytosine content of 11.8% using ligation based assembly and polymerase chain reaction-based assembly respectively, via the use of multiple strategies addressing the adenine/thymine rich nature of the fragment. Sequences can be simply chopped and assembled without Tm optimization. Smaller amount of ligation products as templates in Interference Free polymerase chain reaction yielded markedly more than or equal amount of subassembly products as using larger amount of ligation products, and longer extension time was required for successful subassembly. Longer time at low annealing temperature also had obvious effects on polymerase chain reaction amplifications. No full-length products could be generated without initial oligonucleotide sub-pooling for both approaches. The chemical synthesis of extraordinary adenine/thymine rich DNA could enable researchers to assemble synthetic modules, to study and to access the repetitive DNA such as heterochromatin regions which harbor important functional elements.
Proceedings of the National Academy of Sciences, India Section B: Biological Sciences – Springer Journals
Published: Jan 25, 2017
Read and print from thousands of top scholarly journals.
Already have an account? Log in
Bookmark this article. You can see your Bookmarks on your DeepDyve Library.
To save an article, log in first, or sign up for a DeepDyve account if you don’t already have one.
Copy and paste the desired citation format or use the link below to download a file formatted for EndNote
Access the full text.
Sign up today, get DeepDyve free for 14 days.
All DeepDyve websites use cookies to improve your online experience. They were placed on your computer when you launched this website. You can change your cookie settings through your browser.