Evidence map›Paper›PMID 37884513›Full record

ArticleNature communications2023

Enzymatic synthesis and nanopore sequencing of 12-letter supernumerary DNA.

Hinako Kawabe, Christopher A Thomas, Shuichi Hoshika, Myong-Jung Kim, Myong-Sang Kim, Logan Miessner, Nicholas Kaplan, Jonathan M Craig, Jens H Gundlach, Andrew H Laszlo and 2 more

Abstract read
In one paragraph

Article in Nature communications, 2023. 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
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  11. Article
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  15. Article
  16. Review
  17. DNA storage: The future direction for medical cold data storage.Synthetic and systems biotechnology · 2025
    Review
  18. Article
  19. Review
  20. Article
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

12 authors.

Hinako KawabeDepartment of Chemical Engineering, University of Washington, Seattle, WA, 98195, USA.ORCID 0000-0001-6296-7979
Christopher A ThomasDepartment of Physics, University of Washington, Seattle, WA, 98195, USA.ORCID 0000-0003-2434-5049
Shuichi HoshikaFoundation for Applied Molecular Evolution, Alachua, FL, 32615, USA.ORCID 0000-0001-9128-1183
Myong-Jung KimFoundation for Applied Molecular Evolution, Alachua, FL, 32615, USA.
Myong-Sang KimFirebird Biomolecular Sciences LLC, Alachua, FL, 32615, USA.
Logan MiessnerDepartment of Biochemistry, University of Washington, Seattle, WA, 98195, USA.
Nicholas KaplanDepartment of Chemical Engineering, University of Washington, Seattle, WA, 98195, USA.
Jonathan M CraigDepartment of Physics, University of Washington, Seattle, WA, 98195, USA.ORCID 0000-0003-4791-5112
Jens H GundlachDepartment of Physics, University of Washington, Seattle, WA, 98195, USA.ORCID 0000-0002-0773-8038
Andrew H LaszloDepartment of Physics, University of Washington, Seattle, WA, 98195, USA.ORCID 0000-0002-7853-0533
Steven A BennerFoundation for Applied Molecular Evolution, Alachua, FL, 32615, USA.
Jorge A MarchandDepartment of Chemical Engineering, University of Washington, Seattle, WA, 98195, USA. jmarcha@uw.edu.ORCID 0000-0002-7765-610X

Funding

Nanopore sequencing of DNA with MspAR01HG005115 · NHGRI · UNIVERSITY OF WASHINGTON · PI GUNDLACH, JENS, LASZLO, ANDREW · 2009 to 2024
$14.0M
Technology Development Coordinating CenterU24HG011735 · NHGRI · JACKSON LABORATORY · PI Mark D ADAMS · 2021 to 2026
$8.1M
Transforming Life Sciences: Artificial LifeR01GM128186 · NIGMS · FOUNDATION FOR APPLIED MOLECULAR EVOLUTN · PI BENNER, STEVEN A · 2017 to 2021
$3.4M
NHGRI NIH HHS R01 HG005115NHGRI NIH HHS U24 HG011735NIGMS NIH HHS R01 GM128186
6 · The paper itself

Abstract

The 4-letter DNA alphabet (A, T, G, C) as found in Nature is an elegant, yet non-exhaustive solution to the problem of storage, transfer, and evolution of biological information. Here, we report on strategies for both writing and reading DNA with expanded alphabets composed of up to 12 letters (A, T, G, C, B, S, P, Z, X, K, J, V). For writing, we devise an enzymatic strategy for inserting a singular, orthogonal xenonucleic acid (XNA) base pair into standard DNA sequences using 2'-deoxy-xenonucleoside triphosphates as substrates. Integrating this strategy with combinatorial oligos generated on a chip, we construct libraries containing single XNA bases for parameterizing kmer basecalling models for commercially available nanopore sequencing. These elementary steps are combined to synthesize and sequence DNA containing 12 letters - the upper limit of what is accessible within the electroneutral, canonical base pairing framework. By introducing low-barrier synthesis and sequencing strategies, this work overcomes previous obstacles paving the way for making expanded alphabets widely accessible.

Indexed as

Nanopore SequencingBase PairingDNAProtein BiosynthesisDNA

Identifiers

PMID37884513
PMCPMC10603101

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.