Literature DB >> 36029395

Oligo replication advantage driven by GC content and Gibbs free energy.

Hongyan Qiao1,2, Yanmin Gao1,2, Qian Liu1,2, Yanan Wei1,2, Jiaojiao Li1,2, Zhaoguan Wang1,2, Hao Qi3,4,5.   

Abstract

Large scale DNA oligo pools are emerging as a novel material in a variety of advanced applications. However, GC content and length cause significant bias in amplification of oligos. We systematically explored the amplification of one oligo pool comprising of over ten thousand distinct strands with moderate GC content in the range of 35-65%. Uniqual amplification of oligos result to the increased Gini index of the oligo distribution while a few oligos greatly increased their proportion after 60 cycles of PCR. However, the significantly enriched oligos all have relatively high GC content. Further thermodynamic analysis demonstrated that a high value of both GC content and Gibbs free energy could improve the replication of specific oligos during biased amplification. Therefore, this double-G (GC content and Gibbs free energy) driven replication advantage can be used as a guiding principle for the sequence design for a variety of applications, particularly for data storage.
© 2022. The Author(s), under exclusive licence to Springer Nature B.V.

Entities:  

Keywords:  DNA amplification; DNA free-energy; DNA storage; Oligo pool

Mesh:

Substances:

Year:  2022        PMID: 36029395     DOI: 10.1007/s10529-022-03295-2

Source DB:  PubMed          Journal:  Biotechnol Lett        ISSN: 0141-5492            Impact factor:   2.716


  25 in total

1.  Length and GC-biases during sequencing library amplification: a comparison of various polymerase-buffer systems with ancient and modern DNA sequencing libraries.

Authors:  Jesse Dabney; Matthias Meyer
Journal:  Biotechniques       Date:  2012-02       Impact factor: 1.993

2.  PCR-amplification of GC-rich regions: 'slowdown PCR'.

Authors:  Ulrich H Frey; Hagen S Bachmann; Jürgen Peters; Winfried Siffert
Journal:  Nat Protoc       Date:  2008       Impact factor: 13.491

3.  'Touchdown' PCR to circumvent spurious priming during gene amplification.

Authors:  R H Don; P T Cox; B J Wainwright; K Baker; J S Mattick
Journal:  Nucleic Acids Res       Date:  1991-07-25       Impact factor: 16.971

4.  Uniform amplification of a mixture of deoxyribonucleic acids with varying GC content.

Authors:  N Baskaran; R P Kandpal; A K Bhargava; M W Glynn; A Bale; S M Weissman
Journal:  Genome Res       Date:  1996-07       Impact factor: 9.043

5.  DNA Fountain enables a robust and efficient storage architecture.

Authors:  Yaniv Erlich; Dina Zielinski
Journal:  Science       Date:  2017-03-03       Impact factor: 47.728

6.  Efficient Biosynthesis of (2S)-Eriodictyol from (2S)-Naringenin in Saccharomyces cerevisiae through a Combination of Promoter Adjustment and Directed Evolution.

Authors:  Song Gao; Xiaoyu Xu; Weizhu Zeng; Sha Xu; Yunbin Lyv; Yue Feng; Guoyin Kai; Jingwen Zhou; Jian Chen
Journal:  ACS Synth Biol       Date:  2020-11-23       Impact factor: 5.110

7.  Bovine serum albumin further enhances the effects of organic solvents on increased yield of polymerase chain reaction of GC-rich templates.

Authors:  Eric M Farell; Gladys Alexandre
Journal:  BMC Res Notes       Date:  2012-05-24

8.  Summarizing and correcting the GC content bias in high-throughput sequencing.

Authors:  Yuval Benjamini; Terence P Speed
Journal:  Nucleic Acids Res       Date:  2012-02-09       Impact factor: 16.971

9.  Direct mutagenesis of thousands of genomic targets using microarray-derived oligonucleotides.

Authors:  Mads T Bonde; Sriram Kosuri; Hans J Genee; Kira Sarup-Lytzen; George M Church; Morten O A Sommer; Harris H Wang
Journal:  ACS Synth Biol       Date:  2014-06-20       Impact factor: 5.110

10.  Quantifying molecular bias in DNA data storage.

Authors:  Yuan-Jyue Chen; Christopher N Takahashi; Lee Organick; Callista Bee; Siena Dumas Ang; Patrick Weiss; Bill Peck; Georg Seelig; Luis Ceze; Karin Strauss
Journal:  Nat Commun       Date:  2020-06-29       Impact factor: 14.919

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.