Evidence map›Paper›PMID 20121268›Full record

ArticleAccounts of chemical research2010

An integrated system for DNA sequencing by synthesis using novel nucleotide analogues.

Jia Guo, Lin Yu, Nicholas J Turro, Jingyue Ju

Abstract read
In one paragraph

Article in Accounts of chemical research, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

23 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Review
  6. Multiplexed Single-Cell in Situ Protein Profiling.ACS measurement science au · 2022
    Review
  7. Article
  8. Single-cell proteomic analysis.WIREs mechanisms of disease · 2021
    Review
  9. Article
  10. Article
  11. Highly multiplexed single-cellChemical science · 2018
    Article
  12. Single-CellFrontiers in cell and developmental biology · 2018
    Article
  13. Article
  14. Article
  15. New class of 8-aryl-7-deazaguanine cell permeable fluorescent probes.Bioorganic & medicinal chemistry letters · 2015
    Article
  16. Review
  17. Review
  18. Article
  19. Systematic deciphering of cancer genome networks.The Yale journal of biology and medicine · 2012
    Review
  20. Fluorescent hybridization probes for nucleic acid detection.Analytical and bioanalytical chemistry · 2012
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Jia GuoColumbia Genome Center, Columbia University College of Physicians and Surgeons, New York, New York 10032, USA.
Lin Yu
Nicholas J Turro
Jingyue Ju

Funding

An Integrated System for DNA Sequencing by SynthesisR01HG003582 · NHGRI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI JU, JINGYUE · 2004 to 2009
$4.3M
Molecular Engineering Approach to Study Long Term Synaptic PlasticityR01NS060762 · NINDS · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI JU, JINGYUE · 2008 to 2011
$2.3M
Single Molecule DNA Sequencing by Fluorescent Nucleotide Reversible TerminatorsR01HG005109 · NHGRI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI JU, JINGYUE · 2009 to 2011
$1.8M
3'-O-Modified Nucleotide Reversible Terminators for PyrosequencingR21HG004404 · NHGRI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI JU, JINGYUE · 2007 to 2008
$644k
NHGRI NIH HHS R01 HG003582NHGRI NIH HHS R01HG003582NHGRI NIH HHS R01 HG005109NHGRI NIH HHS R01HG005109NHGRI NIH HHS R21 HG004404NHGRI NIH HHS R21HG004404NINDS NIH HHS R01 NS060762NINDS NIH HHS R01NS060762
6 · The paper itself

Abstract

The Human Genome Project has concluded, but its successful completion has increased, rather than decreased, the need for high-throughput DNA sequencing technologies. The possibility of clinically screening a full genome for an individual's mutations offers tremendous benefits, both for pursuing personalized medicine and for uncovering the genomic contributions to diseases. The Sanger sequencing method, although enormously productive for more than 30 years, requires an electrophoretic separation step that, unfortunately, remains a key technical obstacle for achieving economically acceptable full-genome results. Alternative sequencing approaches thus focus on innovations that can reduce costs. The DNA sequencing by synthesis (SBS) approach has shown great promise as a new sequencing platform, with particular progress reported recently. The general fluorescent SBS approach involves (i) incorporation of nucleotide analogs bearing fluorescent reporters, (ii) identification of the incorporated nucleotide by its fluorescent emissions, and (iii) cleavage of the fluorophore, along with the reinitiation of the polymerase reaction for continuing sequence determination. In this Account, we review the construction of a DNA-immobilized chip and the development of novel nucleotide reporters for the SBS sequencing platform. Click chemistry, with its high selectivity and coupling efficiency, was explored for surface immobilization of DNA. The first generation (G-1) modified nucleotides for SBS feature a small chemical moiety capping the 3'-OH and a fluorophore tethered to the base through a chemically cleavable linker; the design ensures that the nucleotide reporters are good substrates for the polymerase. The 3'-capping moiety and the fluorophore on the DNA extension products, generated by the incorporation of the G-1 modified nucleotides, are cleaved simultaneously to reinitiate the polymerase reaction. The sequence of a DNA template immobilized on a surface via click chemistry is unambiguously identified with this chip-SBS system. The second generation (G-2) SBS system was developed based on the concept that the closer the structures of the added nucleotide and the primer are to their natural counterparts, the more faithfully the polymerase would incorporate the nucleotide. In this approach, the polymerase reaction is performed with the combination of 3'-capped nucleotide reversible terminators (NRTs) and cleavable fluorescent dideoxynucleotides (ddNTPs). By sacrifice of a small amount of the primers permanently terminated by ddNTPs, the majority of the primers extended by the reversible terminators are reverted to the natural ones after each sequencing cycle. We have also developed the 3'-capped nucleotide reversible terminators to solve the problem of deciphering the homopolymeric regions of the template in conventional pyrosequencing. The 3'-capping moiety on the DNA extension product temporarily terminates the polymerase reaction, which allows only one nucleotide to be incorporated during each sequencing cycle. Thus, the number of nucleotides in the homopolymeric regions are unambiguously determined using the 3'-capped NRTs. It has been established that millions of DNA templates can be immobilized on a chip surface through a variety of approaches. Therefore, the integration of these high-density DNA chips with the molecular-level SBS approaches described in this Account is expected to generate a high-throughput and accurate DNA sequencing system with wide applications in biological research and health care.

Indexed as

DNADNA-Directed DNA PolymeraseDNA PrimersFluorescent DyesNucleotidesSequence Analysis, DNADNADNA-Directed DNA PolymeraseDNA PrimersFluorescent DyesNucleotides

Identifiers

PMID20121268
PMCPMC2857541

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.