Exogenous artificial DNA forms chromatin structure with active transcription in yeast
Open accessAbstract
Yeast artificial chromosomes (YACs) are important tools for sequencing, gene cloning, and transferring large quantities of genetic information. However, the structure and activity of YAC chromatin, as well as the unintended impacts of introducing foreign DNA sequences on DNA-associated biochemical events, have not been widely explored. Here, we showed that abundant genetic elements like TATA box and transcription factor-binding motifs occurred unintentionally in a previously reported data-carrying chromosome (dChr). In addition, we used state-of-the-art sequencing technologies to comprehensively profile the genetic, epigenetic, transcriptional, and proteomic characteristics of the exogenous dChr. We found that the data-carrying DNA formed active chromatin with high chromatin accessibility and H3K4 tri-methylation levels. The dChr also displayed highly pervasive transcriptional ability and transcribed hundreds of noncoding RNAs. The results demonstrated that exogenous artificial chromosomes formed chromatin structures and did not remain as naked or loose plasmids. A better understanding of the YAC chromatin nature will improve our ability to design better data-storage chromosomes.
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
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.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The high fidelity of dChr replication could be achieved due to its chromatin-like structure formed in vivo.
“The high fidelity of dChr replication could be achieved due to its chromatin-like structure formed in vivo [70].”
From DNA Data Storage. (2023) · cites this paper as [70]
The Introduction reports stable dChr replication and no mutations in tested samples after 100 generations. The chromatin-results section reports that dChr formed chromatin with histones in vivo. The paper does not attribute replication fidelity to that chromatin structure; its Introduction instead suggests that the dChr’s Rabl configuration may contribute to self-replication. (LLM, conf=0.84)
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Comprehensive Mapping of Long-Range Interactions Reveals Folding Principles of the Human Genome
Lieberman-Aiden, E., van Berkum, N. L., Williams, L., Imakaev, M., Ragoczy, T., Telling, A., Amit, I., Lajoie, B. R., Sabo, P. J., Dorschner, M. O., et al. (2009) · Science · doi:10.1126/science.1181369 · Cited by 8,898 · see citing works
Gene ontology analysis for RNA-seq: accounting for selection bias
Young, M. D., Wakefield, M. J., Smyth, G. K., & Oshlack, A. (2010) · Genome Biology · doi:10.1186/gb-2010-11-2-r14 · Cited by 7,107 · see citing works
Bailey, T., Johnson, J., Grant, C. E., & Noble, W. S. (2015) · Nucleic Acids Res. · doi:10.1093/nar/gkv416 · Cited by 4,916 · see citing works
FIMO: scanning for occurrences of a given motif
Grant, C. E., Bailey, T. L., & Noble, W. S. (2011) · Bioinformatics · doi:10.1093/bioinformatics/btr064 · Cited by 4,247 · see citing works
Production of the antimalarial drug precursor artemisinic acid in engineered yeast
Ro, D.-K., Paradise, E. M., Ouellet, M., Fisher, K. J., Newman, K. L., Ndungu, J. M., Ho, K. A., Eachus, R. A., Ham, T. S., Kirby, J., et al. (2006) · Nature · doi:10.1038/nature04640 · Cited by 2,805 · see citing works
Creation of a Bacterial Cell Controlled by a Chemically Synthesized Genome
Gibson, D. G., Glass, J. I., Lartigue, C., Noskov, V. N., Chuang, R.-Y., Algire, M. A., Benders, G. A., Montague, M. G., Ma, L., Moodie, M. M., et al. (2010) · Science · doi:10.1126/science.1190719 · Cited by 2,638 · see citing works
HiC-Pro: an optimized and flexible pipeline for Hi-C data processing.
Servant, N., Varoquaux, N., Lajoie, B. R., Viara, E., Chen, C.-J., Vert, J.-P., Heard, E., Dekker, J., & Barillot, E. (2015) · Genome Biology · doi:10.1186/s13059-015-0831-x · Cited by 2,565 · see citing works
An improved ATAC-seq protocol reduces background and enables interrogation of frozen tissues
Corces, M. R., Trevino, A. E., Hamilton, E. G., Greenside, P. G., Sinnott-Armstrong, N. A., Vesuna, S., Satpathy, A. T., Rubin, A. J., Montine, K. S., Wu, B., et al. (2017) · Nature Methods · doi:10.1038/nmeth.4396 · Cited by 2,496 · see citing works
Juicebox Provides a Visualization System for Hi-C Contact Maps with Unlimited Zoom
Durand, N. C., Robinson, J., Shamim, M. S., Machol, I., Mesirov, J. P., Lander, E. S., & Aiden, E. L. (2016) · Cell Systems · doi:10.1016/j.cels.2015.07.012 · Cited by 2,335 · see citing works
Chromatin accessibility and the regulatory epigenome
Klemm, S. L., Shipony, Z., & Greenleaf, W. J. (2019) · Nature Reviews Genetics · doi:10.1038/s41576-018-0089-8 · Cited by 1,793 · see citing works
Design and synthesis of a minimal bacterial genome
Hutchison, C. A., Chuang, R.-Y., Noskov, V. N., Assad-Garcia, N., Deerinck, T. J., Ellisman, M. H., Gill, J., Kannan, K., Karas, B. J., Ma, L., et al. (2016) · Science · doi:10.1126/science.aad6253 · Cited by 1,500 · see citing works
Shiraki, T., Kondo, S., Katayama, S., Waki, K., Kasukawa, T., Kawaji, H., Kodzius, R., Watahiki, A., Nakamura, M., Arakawa, T., et al. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2136655100 · Cited by 772 · see citing works
A single-molecule long-read survey of the human transcriptome
Sharon, D., Tilgner, H., Grubert, F., & Snyder, M. (2013) · Nature Biotechnology · doi:10.1038/nbt.2705 · Cited by 701 · see citing works
Identification and Distinct Regulation of Yeast TATA Box-Containing Genes
Basehoar, A. D., Zanton, S. J., & Pugh, B. F. (2004) · Cell · doi:10.1016/s0092-8674(04)00205-3 · Cited by 686 · see citing works
Complete biosynthesis of cannabinoids and their unnatural analogues in yeast
Luo, X., Reiter, M. A., d’Espaux, L., Wong, J., Denby, C. M., Lechner, A., Zhang, Y., Grzybowski, A. T., Harth, S., Lin, W., et al. (2019) · Nature · doi:10.1038/s41586-019-0978-9 · Cited by 676 · see citing works
Total synthesis of Escherichia coli with a recoded genome
Fredens, J., Wang, K., de la Torre, D., Funke, L. F. H., Robertson, W. E., Christova, Y., Chia, T., Schmied, W. H., Dunkelmann, D. L., Beránek, V., et al. (2019) · Nature · doi:10.1038/s41586-019-1192-5 · Cited by 529 · see citing works
Hieter, P. (1985) · Cell · doi:10.1016/0092-8674(85)90152-7 · Cited by 484 · see citing works
Tkach, J. M., Yimit, A., Lee, A. Y., Riffle, M. E., Costanzo, M., Jaschob, D., Hendry, J. A., Ou, J., Moffat, J., Boone, C. M., et al. (2012) · Nature Cell Biology · doi:10.1038/ncb2549 · Cited by 476 · see citing works
Widespread Polycistronic Transcripts in Fungi Revealed by Single-Molecule mRNA Sequencing
Gordon, S., Tseng, E., Salamov, A. A., Zhang, J., Meng, X., Zhao, Z., Kang, D., Underwood, J. G., Grigoriev, I. V., Figueroa, M., et al. (2015) · PLoS ONE · doi:10.1371/journal.pone.0132628 · Cited by 403 · see citing works
Promoter2.0: for the recognition of PolII promoter sequences.
Knudsen, S. (1999) · Bioinformatics · doi:10.1093/bioinformatics/15.5.356 · Cited by 391 · see citing works
Biosynthesis of medicinal tropane alkaloids in yeast
Srinivasan, P., & Smolke, C. D. (2020) · Nature · doi:10.1038/s41586-020-2650-9 · Cited by 375 · see citing works
Cartography of neurexin alternative splicing mapped by single-molecule long-read mRNA sequencing
Treutlein, B., Gokce, O., Quake, S. R., & Südhof, T. C. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1403244111 · Cited by 348 · see citing works
The small peptide world in long noncoding RNAs
Choi, S.-W., Kim, H., & Nam, J. (2018) · Briefings in Bioinformatics · doi:10.1093/bib/bby055 · Cited by 289 · see citing works
“Perfect” designer chromosome V and behavior of a ring derivative.
Xie, Z.-X., Li, B.-Z., Mitchell, L. A., Wu, Y., Qi, X., Jin, Z., Jia, B., Wang, X., Zeng, B.-X., Liu, H.-M., et al. (2017) · Science · doi:10.1126/science.aaf4704 · Cited by 255 · see citing works
Self-citationBug mapping and fitness testing of chemically synthesized chromosome X
Wu, Y., Li, B., Zhao, M., MITCHELL, L. A., Xie, Z., Lin, Q.-H., Wang, X., Xiao, W., Wāng, Y., Zhou, X., et al. (2017) · Science · doi:10.1126/science.aaf4706 · Cited by 239 · see citing works
Self-citationKouprina, N., & Larionov, V. (2008) · Nature Protocols · doi:10.1038/nprot.2008.5 · Cited by 234 · see citing works
Engineering the ribosomal DNA in a megabase synthetic chromosome
Zhang, W., Zhao, G., Luo, Z., Lin, Y., Wang, L., Guo, Y., Wang, A., Jiang, S., Jiang, Q., Gong, J., et al. (2017) · Science · doi:10.1126/science.aaf3981 · Cited by 232 · see citing works
Self-citationDeep functional analysis of synII, a 770-kilobase synthetic yeast chromosome.
Shen, Y., Wang, Y., Chen, T., Gao, F., Gong, J., Abramczyk, D., Walker, R., Zhao, H., Chen, S., Liu, W., et al. (2017) · Science · doi:10.1126/science.aaf4791 · Cited by 202 · see citing works
Self-citationDefining synonymous codon compression schemes by genome recoding
Wang, K., Fredens, J., Brunner, S. F., Kim, S. H., Chia, T., & Chin, J. W. (2016) · Nature · doi:10.1038/nature20124 · Cited by 172 · see citing works
An Artificial Chromosome for Data Storage
Chen, W., Han, M., Zhou, J., Ge, Q., Wang, P., Zhang, X., Zhu, S., Song, L., & Yuan, Y. (2021) · National Science Review · doi:10.1093/nsr/nwab028 · Cited by 136 · see citing works
Self-citationComprehensive comparative analysis of 5′-end RNA-sequencing methods
Adiconis, X., Haber, A. L., Simmons, S., Levy‐Moonshine, A., Ji, Z., Busby, M., Shi, X., Jacques, J., Lancaster, M. A., Pan, J. Q., et al. (2018) · Nature Methods · doi:10.1038/s41592-018-0014-2 · Cited by 121 · see citing works
Chromatin regulation at the frontier of synthetic biology
Keung, A. J., Joung, J. K., Khalil, A. S., & Collins, J. J. (2015) · Nature Reviews Genetics · doi:10.1038/nrg3900 · Cited by 106 · see citing works
Copy number control by a yeast centromere.
Tschumper, G., & Carbon, J. (1983) · Gene · doi:10.1016/0378-1119(83)90054-9 · Cited by 94 · see citing works
Transfer of YACs up to 2.3 Mb intact into human cells with polyethylenimine
Marschall, P., Malik, N., & Larin, Z. (1999) · Gene Therapy · doi:10.1038/sj.gt.3300975 · Cited by 85 · see citing works
Zhou, J., Wu, R., Xue, X., & Qin, Z. (2016) · Nucleic Acids Research · doi:10.1093/nar/gkw475 · Cited by 82 · see citing works
Self-citationtagHi-C Reveals 3D Chromatin Architecture Dynamics during Mouse Hematopoiesis
Zhang, C., Xu, Z., Yang, S., Sun, G., Jia, L., Zheng, Z., Gu, Q., Tao, W., Cheng, T., Li, C., et al. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.108206 · Cited by 72 · see citing works
Self-citationThe dynamic three-dimensional organization of the diploid yeast genome
Kim, S., Liachko, I., Brickner, D. G., et al. (2017) · eLife · doi:10.7554/elife.23623 · Cited by 67 · see citing works
Pervasive and dynamic transcription initiation in Saccharomyces cerevisiaePreprint
Lu, Z., & Lin, Z. (2019) · Genome Research · doi:10.1101/gr.245456.118 · Cited by 67 · see citing works
Saccharomyces cerevisiae Shuttle vectors
Gnügge, R., & Rudolf, F. (2017) · Yeast · doi:10.1002/yea.3228 · Cited by 66 · see citing works
From Mapping to Sequencing, Post-sequencing and Beyond
Sasaki, T., Matsumoto, T., Antonio, B. A., et al. (2005) · Plant and Cell Physiology · doi:10.1093/pcp/pci503 · Cited by 64 · see citing works
ChIP–Quantitative Polymerase Chain Reaction (ChIP-qPCR)Preprint
Kim, T. H., & Dekker, J. (2018) · Cold Spring Harbor Protocols · doi:10.1101/pdb.prot082628 · Cited by 60 · see citing works
YAC transgenics and the study of genetics and human disease
Lamb, B. T., & Gearhart, J. D. (1995) · Current Opinion in Genetics & Development · doi:10.1016/0959-437x(95)80049-2 · Cited by 58 · see citing works
Chong, S. Y., Cutler, S., Lin, J., Tsai, C.-H., Tsai, H., Biggins, S., Tsukiyama, T., Lo, Y., & Kao, C.-F. (2020) · Nature Communications · doi:10.1038/s41467-020-14595-4 · Cited by 56 · see citing works
Humanizing the yeast origin recognition complex
Lee, C. S. K., Cheung, M. F., Li, J., et al. (2021) · Nature Communications · doi:10.1038/s41467-020-20277-y · Cited by 49 · see citing works
The Rabl configuration limits topological entanglement of chromosomes in budding yeast
Pouokam, M., Cruz, B., Burgess, S. M., Segal, M. R., Vázquez, M., & Arsuaga, J. (2019) · Scientific Reports · doi:10.1038/s41598-019-42967-4 · Cited by 40 · see citing works
Wang, R., Mozziconacci, J., Bancaud, A., et al. (2015) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2015.04.004 · Cited by 37 · see citing works
In-Depth Proteome Coverage by Improving Efficiency for Membrane Proteome Analysis
Zhao, Q., Fang, F., Shan, Y., Sui, Z., Zhao, B., Liang, Z., Zhang, L., & Zhang, Y. (2017) · Analytical Chemistry · doi:10.1021/acs.analchem.6b04232 · Cited by 36 · see citing works
Self-citationA supernumerary designer chromosome for modular in vivo pathway assembly in Saccharomyces cerevisiae
Postma, E. D., Dashko, S., van Breemen, L., Parkins, S. K. T., van den Broek, M. A., Daran, J.-M. G., & Daran-Lapujade, P. A. S. (2020) · Nucleic Acids Research · doi:10.1093/nar/gkaa1167 · Cited by 36 · see citing works
Molecular Dynamics Simulation-assisted Ionic Liquid Screening for Deep Coverage Proteome Analysis
Fang, F., Zhao, Q., Chu, H., Liu, M., Zhao, B., Liang, Z., Zhang, L., Li, G., Wang, L., Qin, J., et al. (2020) · Molecular & Cellular Proteomics · doi:10.1074/mcp.tir119.001827 · Cited by 35 · see citing works
Self-citationNon-coding transcription by RNA polymerase II in yeast: Hasard or nécessité?
Tudek, A., Candelli, T., & Libri, D. (2015) · Biochimie · doi:10.1016/j.biochi.2015.04.020 · Cited by 26 · see citing works
Sylvain, M.-A., Liang, X. B., Hellauer, K., & Turcotte, B. (2011) · Genetics · doi:10.1534/genetics.110.126003 · Cited by 23 · see citing works
Widespread Polycistronic Transcripts In Fungi Revealed By Single-Molecule Mrna Sequencing
Gordon, S., Tseng, E., Salamov, A. A., et al. (2016) · Zenodo (CERN European Organization for Nuclear Research) · doi:10.5281/zenodo.165839 · Cited by 15 · see citing works
Kannan, K., & Gibson, D. G. (2017) · Science · doi:10.1126/science.aam9739 · Cited by 14 · see citing works
Self-replicating digital data storage with synthetic chromosomes
Lu, X., & Ellis, T. (2021) · National Science Review · doi:10.1093/nsr/nwab086 · Cited by 12 · see citing works
Long Noncoding RNAs in Yeast Cells and Differentiated Subpopulations of Yeast Colonies and Biofilms
Wilkinson, D., Váchová, L., Hlaváček, O., et al. (2018) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2018/4950591 · Cited by 10 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Buko, T., Tuczko, N., & Ishikawa, T. (2023) · BioTech · doi:10.3390/biotech12020044 · Cited by 21 · see citing works
“The high fidelity of dChr replication could be achieved due to its chromatin-like structure formed in vivo [70].”
Background
- Authors
- Zhou, J., Zhang, C., Wei, R., Han, M., Wang, S., Yang, K., Zhang, L., Chen, W., Wen, M., Li, C., Tao, W., & Yuan, Y.-J.
- Affiliations
- Tianjin University (CN)
- Peking University (CN)
- Dalian Institute of Chemical Physics (CN)
- Corresponding author
- Tao, Wei
- Yuan, Ying-Jin
- ORCID
- Venue
- Science China Life Sciences
- Published
- 2021-12-27
- Volume
- 65
- Issue
- 5
- Pages
- 851-860
- ISSN
- 1674-7305 (ISSN-L)
- 1869-1889
- OpenAlex
- W4205424159
- Cited by
- 24
- References
- 55
- Citations by year
- 2026: 7 · 2025: 1 · 2024: 5 · 2023: 3 · 2022: 8
- FWCI
- 1.26
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Locations
- Science China Life Sciences (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Funders
- National Key Research and Development Program of China (2121YFA0909300)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fungal and yeast genetics research
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Chromosomal and Genetic Variations
- Keywords
- yeast artificial chromosomes, artificial DNA, chromatin structure, chromatin accessibility, H3K4 trimethylation, pervasive transcription, non-coding RNA, epigenetic profiling, transcription factor binding motifs, TATA box
- MeSH terms
- Chromatin, DNA, Saccharomyces cerevisiae, Chromosomes, Artificial, Yeast, Proteomics
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