The DOI matches its Crossref record; 83 of the 83 references it cites were found in a registry or an index.
Tet2 and Tet3 cooperate with B-lineage transcription factors to regulate DNA modification and chromatin accessibility
Open accessAbstract
Ten-eleven translocation (TET) enzymes oxidize 5-methylcytosine, facilitating DNA demethylation and generating new epigenetic marks. Here we show that concomitant loss of Tet2 and Tet3 in mice at early B cell stage blocked the pro- to pre-B cell transition in the bone marrow, decreased Irf4 expression and impaired the germline transcription and rearrangement of the Igκ locus. Tet2/3-deficient pro-B cells showed increased CpG methylation at the Igκ 3’ and distal enhancers that was mimicked by depletion of E2A or PU.1, as well as a global decrease in chromatin accessibility at enhancers. Importantly, re-expression of the Tet2 catalytic domain in Tet2/3-deficient B cells resulted in demethylation of the Igκ enhancers and restored their chromatin accessibility. Our data suggest that TET proteins and lineage-specific transcription factors cooperate to influence chromatin accessibility and Igκ enhancer function by modulating the modification status of DNA.
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“which can physically interact with the myeloid master transcription factor (TF; Supplementary Fig. S5K and S5L; ref. 34).”
From PU.1-Dependent Enhancer Inhibition Separates Tet2 -Deficient Hematopoiesis from Malignant Transformation (2022) · cites this paper as [34]
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“Tet2 binds and governs site-specific DNA demethylation upon being recruited to the chromatin by DNA-binding TF, such as RUNX1 (51) or PU.1 (34)”
From PU.1-Dependent Enhancer Inhibition Separates Tet2 -Deficient Hematopoiesis from Malignant Transformation (2022) · cites this paper as [34]
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Citations
Cites
Fast gapped-read alignment with Bowtie 2
Langmead, B., & Salzberg, S. L. (2012) · Nature Methods · doi:10.1038/nmeth.1923 · Cited by 56,400
An integrated encyclopedia of DNA elements in the human genome
The ENCODE Project Consortium (2012) · Nature · doi:10.1038/nature11247 · Cited by 18,072
Heinz, S., Benner, C., Spann, N., Bertolino, E., Lin, Y. C., Laslo, P., Cheng, J. X., Murre, C., Singh, H., & Glass, C. K. (2010) · Molecular Cell · doi:10.1016/j.molcel.2010.05.004 · Cited by 13,382
deepTools2: a next generation web server for deep-sequencing data analysis
Ramírez, F., Ryan, D. P., Grüning, B., Bhardwaj, V., Kilpert, F., Richter, A. S., Heyne, S., Dündar, F., & Manke, T. (2016) · Nucleic Acids Research · doi:10.1093/nar/gkw257 · Cited by 8,096
Buenrostro, J. D., Giresi, P. G., Zaba, L. C., Chang, H. Y., & Greenleaf, W. J. (2013) · Nature Methods · doi:10.1038/nmeth.2688 · Cited by 6,422
Conversion of 5-Methylcytosine to 5-Hydroxymethylcytosine in Mammalian DNA by MLL Partner TET1
Tahiliani, M., Koh, K. P., Shen, Y., Pastor, W. A., Bandukwala, H., Brudno, Y., Agarwal, S., Iyer, L. M., Liu, D. R., Aravind, L., et al. (2009) · Science · doi:10.1126/science.1170116 · Cited by 5,836
Self-citationHistone H3K27ac separates active from poised enhancers and predicts developmental state
Creyghton, M. P., Cheng, A. W., Welstead, G. G., Kooistra, T., Carey, B. W., Steine, E. J., Hanna, J., Lodato, M. A., Frampton, G. M., Sharp, P. A., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1016071107 · Cited by 4,302
Tet proteins can convert 5-methylcytosine to 5-formylcytosine and 5-carboxylcytosine
Ito, S., Shen, L., Dai, Q., Wu, S. C., Collins, L. B., Swenberg, J. A., He, C., & Zhang, Y. (2011) · Science · doi:10.1126/science.1210597 · Cited by 3,451
Tet-Mediated Formation of 5-Carboxylcytosine and Its Excision by TDG in Mammalian DNA
He, Y., Li, B.-Z., Li, Z., Liu, P., Wang, Y., Tang, Q., Ding, J., Jia, Y., Chen, Z., Li, L., et al. (2011) · Science · doi:10.1126/science.1210944 · Cited by 2,776
The accessible chromatin landscape of the human genome
Thurman, R. E., Rynes, E., Humbert, R., Vierstra, J., Maurano, M. T., Haugen, E., Sheffield, N. C., Stergachis, A. B., Wang, H., Vernot, B., et al. (2012) · Nature · doi:10.1038/nature11232 · Cited by 2,679
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Shi, Y., Zhu, Z., Chen, Q., & Chen, X. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1363426 · Cited by 10
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Wang, Q., Lin, Y., Zhang, B., Wu, J., Roy, S., Ratiu, J. J., Xu, Y., Dai, M., Hale, L. P., Xiong, Y., et al. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2014308117 · Cited by 9
Yang, M., Yi, P., Jiang, J., Zhao, M., Wu, H., & Lu, Q. (2021) · International Reviews of Immunology · doi:10.1080/08830185.2021.1964498 · Cited by 9
Chen, S., Wang, J., Wang, Q., Ping, Y., Yang, T., Ma, K., Pan, S., Bi, Y., Bai, H., & Chang, G. (2025) · Journal of Virology · doi:10.1128/jvi.02003-24 · Cited by 8
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Lee, M., Li, J., Fang, S., Zhang, J., Vo, A. T. T., Han, W., Zeng, H., Isgandarova, S., Martinez-Moczygemba, M., Han, W., et al. (2020) · Research Square · doi:10.21203/rs.3.rs-55173/v1
Self-citationTaniuchi, I. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.735164859.793557257
Winoto, A. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.735164859.793557834
Rouse, B. T. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.735164859.793558438
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Aivalioti, M. M., Bartholdy, B., Pradhan, K., Bhagat, T. D., Zintiridou, A., Jeong, J. J., Thiruthuvanathan, V. J., Pujato, M. A., Paranjpe, A., Zhang, C., et al. (2023) · doi:10.1158/2643-3230.c.6550979.v1
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Roos‐Weil, D. (2018) · theses.fr (ABES) · doi:10.70675/1030cb13z12b8z4f7cz8f8az165206a6209a
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Guida, N., Ruggiero, S., Serani, A., Sisalli, M. J., Mascolo, L., Sanguigno, L., Ferrante, A., Cuomo, O., D’Apolito, E., Laudati, G., et al. (2026) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2026.119505
Li, S., Yibo, P., Yang, Z., Li, X., Xu, Z., Rivera, C. E., & Casali, P. (2026) · Cell Reports · doi:10.1016/j.celrep.2026.117370 · Cited by 1
Lau, L., Lal, S., Fan, J., Pease, N. A., & Singh, H. (2026) · eLife · doi:10.64898/2026.06.15.732353
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Metadata
- Authors
- Lio, C.-W., Zhang, J., González-Avalos, E., Hogan, P. G., Chang, X., & Rao, A.
- Affiliations
- Division of Signaling and Gene Expression, San Diego, United States
- Shanghai Jiao Tong University (CN)
- University of California San Diego (US)
- Corresponding author
- Chang, Xing
- Rao, Anjana
- Venue
- eLife
- Publisher
- eLife Sciences Publications, Ltd
- Published
- 2016-11-21
- Volume
- 5
- ISSN
- 2050-084X (ISSN-L)
- PMC
- PMC5142813
- OpenAlex
- W2552742463
- Cited by
- 170
- References
- 83
- Citations by year
- 2026: 9 · 2025: 11 · 2024: 14 · 2023: 14 · 2022: 25 · 2021: 22 · 2020: 24 · 2019: 22 · 2018: 21 · 2017: 8
- FWCI
- 8.84
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- eLife (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- Cancer Research Institute (Irvington Postdoctoral Fellowship)
- Ministry of Science and Technology of the People's Republic of China (2014CB943600)
- National Institutes of Health (AI44432, CA151535)
- Leukemia and Lymphoma Society (6187-12)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Epigenetics and DNA Methylation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Keywords
- TET2, TET3, B cell development, IRF4, germline transcription, DNA demethylation, 5-methylcytosine oxidation, CpG methylation, E2A, PU.1, transcription factor cooperation, bone marrow
- MeSH terms
- Interferon Regulatory Factor-4, Animals, B-Lymphocytes, Cell Differentiation, Chromatin, DNA, DNA-Binding Proteins, Gene Expression Regulation, Proto-Oncogene Proteins, Transcription, Genetic, 5-Methylcytosine, Dioxygenases, Interferon Regulatory Factors, Mice, Gene Knockout Techniques
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