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Capillary Electrophoresis-Based Functional Genomics Screening to Discover Novel Archaeal DNA Modifying Enzymes
Open accessAbstract
This study provides a rapid, simple, high-throughput method to discover novel archaeal nucleic acid modifying enzymes by utilizing a fosmid genomic library, next-generation sequencing, and capillary electrophoresis. The method described here provides the details necessary to create 384-well fosmid library plates from Thermococcus kodakarensis genomic DNA, sequences of 384-well fosmids plates using Illumina next-generation sequencing, and performed high-throughput functional read-out assays using capillary electrophoresis to identify a variety of nucleic acid modifying activities, including DNA cleavage and ligation.
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In vivo rNMP incorporation events range from 200 to 2,200 or more per round of chromosomal replication in various bacterial species.
“in vivo incorporation events range from 200 to 2,200 or more rNMPs per round of chromosomal replication in various bacterial species”
From Ribonucleotide errors, RNase HII, and ribonucleotide excision repair (2026) · cites this paper as Zatopek et al. 2022
The Results section on RNaseH2 describes cleavage of a ribonucleotide embedded in a DNA substrate, but gives no in vivo incorporation rate. Searches for the 200–2,200 range and for bacterial chromosomal replication frequencies found no passage in our copy addressing the claimed numbers or species comparison. Page numbers were not available. (LLM, conf=0.76)
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Cites
Asgard archaea illuminate the origin of eukaryotic cellular complexity
Zaremba-Niedzwiedzka, K., Caceres, E. F., Saw, J. H., Bäckström, D., Juzokaite, L., Vancaester, E., Seitz, K. W., Anantharaman, K., Starnawski, P., Kjeldsen, K. U., et al. (2017) · Nature · doi:10.1038/nature21031 · Cited by 1,226
Novel Division Level Bacterial Diversity in a Yellowstone Hot Spring
Hugenholtz, P., Pitulle, C., Hershberger, K. L., & Pace, N. R. (1998) · Journal of Bacteriology · doi:10.1128/jb.180.2.366-376.1998 · Cited by 891
Major New Microbial Groups Expand Diversity and Alter our Understanding of the Tree of Life
Castelle, C. J., & Banfield, J. F. (2018) · Cell · doi:10.1016/j.cell.2018.02.016 · Cited by 595
The growing tree of Archaea: new perspectives on their diversity, evolution and ecology
Adam, P. S., Borrel, G., Brochier‐Armanet, C., & Gribaldo, S. (2017) · The ISME Journal · doi:10.1038/ismej.2017.122 · Cited by 394
Quantifying the accessibility of the metagenome by random expression cloning techniques
Gabor, E. M., Alkema, W. B. L., & Janssen, D. B. (2004) · Environmental Microbiology · doi:10.1111/j.1462-2920.2004.00640.x · Cited by 267
Intervening sequences in an Archaea DNA polymerase gene.
Perler, F. B., Comb, D. G., Jack, W. E., Moran, L. S., Qiang, B., Kucera, R. B., Benner, J., Slatko, B. E., Nwankwo, D. O., & Hempstead, S. K. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.12.5577 · Cited by 188
Functional metagenomics of extreme environments
Mirete, S., Morgante, V., & González‐Pastor, J. E. (2016) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2016.01.017 · Cited by 142
Metagenomics of Thermophiles with a Focus on Discovery of Novel Thermozymes
DeCastro, M.-E., Rodriguez-Belmonte, E. M., & González-Siso, M.-I. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2016.01521 · Cited by 129
Uemori, T., Sato, Y., Kato, I., Doi, H., & Ishino, Y. (1997) · Genes to Cells · doi:10.1046/j.1365-2443.1997.1380336.x · Cited by 127
Komori, K., Sakae, S., Shinagawa, H., Morikawa, K., & Ishino, Y. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.16.8873 · Cited by 105
Structural and functional analysis of the archaeal endonuclease Nob1
Veith, T., Martin, R., Wurm, J. P., Weis, B. L., Duchardt, E., Safferthal, C., Hennig, R., Mirus, O., Bohnsack, M. T., Wöhnert, J., et al. (2011) · Nucleic Acids Research · doi:10.1093/nar/gkr1186 · Cited by 77
Leis, B., Angelov, A., Mientus, M., Li, H., Pham, V. T. T., Lauinger, B., Bongen, P., Pietruszka, J., Gonçalves, L. G., Santos, H., et al. (2015) · Frontiers in Microbiology · doi:10.3389/fmicb.2015.00275 · Cited by 74
Gaida, S. M., Sandoval, N. R., Nicolaou, S. A., Chen, Y., Venkataramanan, K. P., & Papoutsakis, E. T. (2015) · Nature Communications · doi:10.1038/ncomms8045 · Cited by 71
Identification of a mismatch-specific endonuclease in hyperthermophilic Archaea
Ishino, S., Nishi, Y., Oda, S., Uemori, T., Sagara, T., Takatsu, N., Yamagami, T., Shirai, T., & Ishino, Y. (2016) · Nucleic Acids Research · doi:10.1093/nar/gkw153 · Cited by 71
Thermostable DNA Polymerase from a Viral Metagenome Is a Potent RT-PCR Enzyme
Moser, M. J., DiFrancesco, R. A., Gowda, K., Klingele, A. J., Sugar, D. R., Stocki, S. L., Mead, D. A., & Schoenfeld, T. W. (2012) · PLoS ONE · doi:10.1371/journal.pone.0038371 · Cited by 67
Greenough, L., Schermerhorn, K. M., Mazzola, L., Bybee, J., Rivizzigno, D., Cantin, E., Slatko, B. E., & Gardner, A. F. (2015) · Nucleic Acids Research · doi:10.1093/nar/gkv899 · Cited by 65
Self-citationProtein Synthesis Using a Reconstituted Cell‐Free System
Tuckey, C., Asahara, H., Zhou, Y., & Chong, S. (2014) · Current Protocols in Molecular Biology · doi:10.1002/0471142727.mb1631s108 · Cited by 64
A DNA Ligase from a Hyperthermophilic Archaeon with Unique Cofactor Specificity
Nakatani, M., Ezaki, S., Atomi, H., & Imanaka, T. (2000) · Journal of Bacteriology · doi:10.1128/jb.182.22.6424-6433.2000 · Cited by 63
A high-throughput assay for the comprehensive profiling of DNA ligase fidelity
Lohman, G. J. S., Bauer, R. J., Nichols, N. M., Mazzola, L., Bybee, J., Rivizzigno, D., Cantin, E., & Evans, T. C. (2015) · Nucleic Acids Research · doi:10.1093/nar/gkv898 · Cited by 61
Self-citationNew Glycosidase Substrates for Droplet-Based Microfluidic Screening
Najah, M., Mayot, E., Wijaya, I., Griffiths, A. D., Ladame, S., & Drevelle, A. (2013) · Analytical Chemistry · doi:10.1021/ac4022709 · Cited by 60
Chang, Y.-C., Hu, Z., Rachlin, J., Anton, B. P., Kasif, S., Roberts, R. J., & Steffen, M. (2016) · Nucleic Acids Research · doi:10.1093/nar/gkv1324 · Cited by 56
Makarova, K. S., Wolf, Y. I., Forterre, P., Prangishvili, D. A., Krupovìč, M., & Koonin, E. V. (2014) · Extremophiles · doi:10.1007/s00792-014-0672-7 · Cited by 54
Towards functional characterization of archaeal genomic dark matter
Makarova, K. S., Wolf, Y. I., & Koonin, E. V. (2019) · Biochemical Society Transactions · doi:10.1042/bst20180560 · Cited by 51
Uracil-DNA glycosylase activities in hyperthermophilic micro-organisms
Koulis, A., Cowan, D. A., Pearl, L. H., & Savva, R. (1996) · FEMS Microbiology Letters · doi:10.1016/0378-1097(96)00325-4 · Cited by 46
Chuzel, L., Ganatra, M. B., Rapp, E., Henrissat, B., & Taron, C. H. (2018) · Journal of Biological Chemistry · doi:10.1074/jbc.ra118.003302 · Cited by 41
Self-citationDefining the RNaseH2 enzyme-initiated ribonucleotide excision repair pathway in Archaea
Heider, M. R., Burkhart, B. W., Santangelo, T. J., & Gardner, A. F. (2017) · Journal of Biological Chemistry · doi:10.1074/jbc.m117.783472 · Cited by 37
Self-citationGehring, A. M., Zatopek, K. M., Burkhart, B. W., Potapov, V., Santangelo, T. J., & Gardner, A. F. (2019) · DNA repair · doi:10.1016/j.dnarep.2019.102767 · Cited by 17
Self-citationTori, K., Ishino, S., Kiyonari, S., Tahara, S., & Ishino, Y. (2013) · PLoS ONE · doi:10.1371/journal.pone.0058497 · Cited by 13
Chapter 44 Important but Little Known (or Forgotten) Artifacts in Protein Biochemistry
Burgess, R. R. (2009) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(09)63044-5 · Cited by 13
Shi, H., Gan, Q., Jiang, D., Wu, Y., Yin, Y., Hou, H., Chen, H., Xu, Y., Miao, L., Yang, Z., et al. (2019) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2019.05.073 · Cited by 9
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Carter, Z. I., O’Brien, W. B., Lund, S. R., & Gardner, A. F. (2024) · PLoS ONE · doi:10.1371/journal.pone.0312743 · Cited by 4
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Caffrey, P. J., Eckenroth, B. E., Burkhart, B. W., Zatopek, K. M., McClung, C. M., Santangelo, T. J., Doublié, S., & Gardner, A. F. (2023) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2023.105503 · Cited by 1
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Cresti, J. R., & Simmons, L. A. (2026) · Critical Reviews in Biochemistry and Molecular Biology · doi:10.1080/10409238.2026.2704628
“Further, in vivo incorporation events range from 200 to 2,200 or more rNMPs per round of chromosomal replication in various bacterial species (Kouzminova et al. 2017; Zatopek et al. 2022).”
Metadata
- Authors
- Zatopek, K. M., Fossa, S. L., Bilotti, K., Caffrey, P. J., Chuzel, L., Gehring, A. M., Lohman, G. J. S., Taron, C. H., & Gardner, A. F.
- Affiliations
- New England Biolabs (United States) (US)
- Corresponding author
- Gardner, Andrew F.
- ORCID
- Venue
- Applied and Environmental Microbiology
- Publisher
- American Society for Microbiology
- Published
- 2022-01-25
- Volume
- 88
- Issue
- 2
- Pages
- e0213721-e0213721
- ISSN
- 0099-2240 (ISSN-L)
- 1098-5336
- PMC
- PMC8788744
- OpenAlex
- W3212220703
- Cited by
- 6
- References
- 30
- Citations by year
- 2026: 1 · 2025: 1 · 2024: 2 · 2023: 2
- FWCI
- 0.31
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Applied and Environmental Microbiology (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Funders
- New England Biolabs
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › CRISPR and Genetic Engineering
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Bacterial Genetics and Biotechnology
- Keywords
- DNA-modifying enzymes, Thermococcus kodakarensis, high-throughput functional screening, DNA endonuclease, AP lyase, enzyme discovery
- MeSH terms
- Escherichia coli, Electrophoresis, Capillary, DNA, Archaeal, Thermococcus, Archaeal Proteins, Genomics
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