The DOI matches its Crossref record; 37 of the 37 references it cites were found in a registry or an index.
T5 exonuclease-dependent assembly offers a low-cost method for efficient cloning and site-directed mutagenesis
Open accessAbstract
The assembly of DNA fragments with homologous arms is becoming popular in routine cloning. For an in vitro assembly reaction, a DNA polymerase is often used either alone for its 3'-5' exonuclease activity or together with a 5'-3' exonuclease for its DNA polymerase activity. Here, we present a 'T5 exonuclease DNA assembly' (TEDA) method that only uses a 5'-3' exonuclease. DNA fragments with short homologous ends were treated by T5 exonuclease and then transformed into Escherichia coli to produce clone colonies. The cloning efficiency was similar to that of the commercial In-Fusion method employing a proprietary DNA polymerase, but higher than that of the Gibson method utilizing T5 exonuclease, Phusion DNA polymerase, and DNA ligase. It also assembled multiple DNA fragments and did simultaneous site-directed mutagenesis at multiple sites. The reaction mixture was simple, and each reaction used 0.04 U of T5 exonuclease that cost 0.25 US cents. The simplicity, cost effectiveness, and cloning efficiency should promote its routine use, especially for labs with a budget constraint. TEDA may trigger further development of DNA assembly methods that employ single exonucleases.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Enzymatic assembly of DNA molecules up to several hundred kilobases
Gibson, D. G., Young, L., Chuang, R.-Y., Venter, J. C., Hutchison, C. A., & Smith, H. O. (2009) · Nature Methods · doi:10.1038/nmeth.1318 · Cited by 9,996
Construction of Escherichia coli K‐12 in‐frame, single‐gene knockout mutants: the Keio collection
Baba, T., Ara, T., Hasegawa, M., Takai, Y., Okumura, Y., Baba, M., Datsenko, K. A., Tomita, M., Wanner, B. L., & Mori, H. (2006) · Molecular Systems Biology · doi:10.1038/msb4100050 · Cited by 7,858
Macromolecular Crowding: Biochemical, Biophysical, and Physiological Consequences
Zimmerman, S. B., & Minton, A. P. (1993) · Annual Review of Biophysics and Biomolecular Structure · doi:10.1146/annurev.bb.22.060193.000331 · Cited by 1,513
Harnessing homologous recombination in vitro to generate recombinant DNA via SLIC
Li, M. Z., & Elledge, S. J. (2007) · Nature Methods · doi:10.1038/nmeth1010 · Cited by 953
DNA assembler, an in vivo genetic method for rapid construction of biochemical pathways
Shao, Z., Zhao, H., & Zhao, H. (2009) · Nucleic Acids Research · doi:10.1093/nar/gkn991 · Cited by 678
Mechanisms of Protein Stabilization and Prevention of Protein Aggregation by Glycerol
Vagenende, V., Yap, M. G. S., & Trout, B. L. (2009) · Biochemistry · doi:10.1021/bi900649t · Cited by 527
Circular Polymerase Extension Cloning of Complex Gene Libraries and Pathways
Quan, J., & Tian, J. (2009) · PLoS ONE · doi:10.1371/journal.pone.0006441 · Cited by 517
SLiCE: a novel bacterial cell extract-based DNA cloning method
Zhang, Y., Werling, U., & Edelmann, W. (2012) · Nucleic Acids Research · doi:10.1093/nar/gkr1288 · Cited by 493
Li, C., Wen, A., Shen, B., Lu, J., Huang, Y., & Chang, Y. (2011) · BMC Biotechnology · doi:10.1186/1472-6750-11-92 · Cited by 484
Gibson, D. G., Benders, G. A., Axelrod, K. C., Zaveri, J., Algire, M. A., Moodie, M., Montague, M. G., Venter, J. C., Smith, H. O., & Hutchison, C. A. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0811011106 · Cited by 477
Cited by
Zhang, K., Eldin, P., Ciesla, J. H., Briant, L., Lentini, J. M., Ramos, J., Cobb, J., Munger, J., & Fu, D. (2024) · eLife · doi:10.7554/elife.90316.3 · Cited by 9
Zhang, K., Eldin, P., Ciesla, J. H., Briant, L., Lentini, J. M., Ramos, J., Cobb, J., Munger, J., & Fu, D. (2023) · doi:10.1101/2023.02.10.527147 · Cited by 3
Sequence-Guided Engineering of a Bacterial Diterpene Synthase Induces Further Cyclization
Wei, X., Ning, W., Huang, P.-S., Nafie, J., Ghiviriga, I., & Rudolf, J. D. (2026) · ACS Catalysis · doi:10.1021/acscatal.6c04391 · Cited by 1
Coordinated regulation of chemotaxis and resistance to copper by CsoR in Pseudomonas putida
He, M., Tao, Y., Mu, K., Feng, H., Fan, Y., Liu, T., Huang, Q., Xiao, Y., & Chen, W. (2025) · eLife · doi:10.7554/elife.100914 · Cited by 1
Metadata
- Authors
- Xia, Y., Li, K., Li, J., Wang, T., Gu, L., & Xun, L.
- Venue
- Nucleic Acids Research
- Publisher
- Oxford University Press (OUP)
- Published
- 2018-11-20
- Volume
- 47
- Issue
- 3
- Pages
- e15-e15
- ISSN
- 0305-1048 (ISSN-L)
- 1362-4962
- OpenAlex
- W2903602386
- Cited by
- 317
- References
- 37
- FWCI
- 4.71
- Type
- journal article
- Language
- en
- Open access
- gold
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: T5 exonuclease-dependent assembly offers a low-cost method for efficient cloning and site-directed mutagenesis. https://app.cochat.ai/papers/10.1093/nar/gky1169
- The paper
- Xia, Y., Li, K., Li, J., Wang, T., Gu, L., & Xun, L. (2019). T5 exonuclease-dependent assembly offers a low-cost method for efficient cloning and site-directed mutagenesis. Nucleic Acids Research. https://doi.org/10.1093/nar/gky1169
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.