The DOI matches its Crossref record; 230 of the 230 references it cites were found in a registry or an index.
Roles of transposable elements in the regulation of mammalian transcription
Open accessAbstract
Transposable elements (TEs) comprise about half of the mammalian genome. TEs often contain sequences capable of recruiting the host transcription machinery, which they use to express their own products and promote transposition. However, the regulatory sequences carried by TEs may affect host transcription long after the TEs have lost the ability to transpose. Recent advances in genome analysis and engineering have facilitated systematic interrogation of the regulatory activities of TEs. In this Review, we discuss diverse mechanisms by which TEs contribute to transcription regulation. Notably, TEs can donate enhancer and promoter sequences that influence the expression of host genes, modify 3D chromatin architecture and give rise to novel regulatory genes, including non-coding RNAs and transcription factors. We discuss how TEs spur regulatory evolution and facilitate the emergence of genetic novelties in mammalian physiology and development. By virtue of their repetitive and interspersed nature, TEs offer unique opportunities to dissect the effects of mutation and genomic context on the function and evolution of cis-regulatory elements. We argue that TE-centric studies hold the key to unlocking general principles of transcription regulation and evolution.
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.
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 cited source says what the claim attributes to it.
In the citing paper
“Contrary to the exogenous infectious agents discussed above, transposable elements are endogenous mobile genetic elements that can move and integrate into different locations within the genome [117,118].”
From What would it take to prove that a chronic infection is a causal agent in Alzheimer’s disease? (2025) · cites this paper as [117]
In the citing paper
“Although this study is focused on identifying CREs, there are other non-coding regulatory mechanisms that could alter gene expression in AD including microRNAs (miRNAs),90 long non-coding RNAs (lncRNAs),91 transposable elements,92 etc., that are not assessed.”
From Single nucleus multiomics identifies ZEB1 and MAFB as candidate regulators of Alzheimer’s disease-specific cis-regulatory elements (2023) · cites this paper as [92]
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
Initial sequencing and analysis of the human genome
International Human Genome Sequencing Consortium, Whitehead Institute for Biomedical Research, C. F. G. R., Lander, E. S., Linton, L. M., Birren, B., Nusbaum, C., Zody, M. C., Baldwin, J., Devon, K., Dewar, K., et al. (2001) · Nature · doi:10.1038/35057062 · Cited by 24,216
Tissue-based map of the human proteome
Uhlén, M., Fagerberg, L., Hallström, B. M., Lindskog, C., Oksvold, P., Mardinoglu, A., Sivertsson, Å., Kampf, C., Sjöstedt, E., Asplund, A., et al. (2015) · Science · doi:10.1126/science.1260419 · Cited by 15,286
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
Topological domains in mammalian genomes identified by analysis of chromatin interactions
Dixon, J. R., Selvaraj, S., Yue, F., Kim, A., Li, Y., Shen, Y., Hu, M., Liu, J. S., & Ren, B. (2012) · Nature · doi:10.1038/nature11082 · Cited by 6,829
Coming of age: ten years of next-generation sequencing technologies
Goodwin, S., McPherson, J. D., & McCombie, W. R. (2016) · Nature Reviews Genetics · doi:10.1038/nrg.2016.49 · Cited by 4,352
Schizophrenia risk from complex variation of complement component 4
Sekar, A., Bialas, A. R., de Rivera, H., Davis, A., Hammond, T. R., Kamitaki, N., Tooley, K., Presumey, J., Baum, M., Van Doren, V., et al. (2016) · Nature · doi:10.1038/nature16549 · Cited by 2,394
Expanded encyclopaedias of DNA elements in the human and mouse genomes
The ENCODE Project Consortium, Abascal, F., Acosta, R., Addleman, N. J., Adrian, J., Afzal, V., Ai, R., Aken, B., Akiyama, J. A., Jammal, O. A., et al. (2020) · Nature · doi:10.1038/s41586-020-2493-4 · Cited by 2,378
An integrated map of structural variation in 2,504 human genomes
Sudmant, P. H., Rausch, T., Gardner, E. J., Handsaker, R. E., Abyzov, A., Huddleston, J., Zhang, Y., Ye, K., Jun, G., Hsi-Yang Fritz, M., et al. (2015) · Nature · doi:10.1038/nature15394 · Cited by 2,354
The diverse roles of DNA methylation in mammalian development and disease
Greenberg, M., & Bourc’his, D. (2019) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-019-0159-6 · Cited by 2,272
Gene Regulation for Higher Cells: A Theory
Britten, R. J., & Davidson, E. H. (1969) · Science · doi:10.1126/science.165.3891.349 · Cited by 2,078
Research works printed but not linked: 2
- Hoyt, S. J. et al. From telomere to telomere: the transcriptional and epigenetic state of human repeat elements. bioRxiv https://doi.org/10.1101/2021.07.12.451456v1 (2021). · DOI
- Carter, T. A. et al. Mosaic cis-regulatory evolution drives transcriptional partitioning of HERVH endogenous retrovirus in the human embryo. bioRxiv https://doi.org/10.1101/2021.07.08.451617v1 (2021). · DOI
Cited by
Sorted by citations
Items 301–400 of 475
Wong, E. W. P., Şahin, M., Yang, R., Lee, U., Zhan, Y. A., Misra, R., Tomas, F. V., Alomran, N., Polyzos, A., Lee, C. J., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.05.31.596845 · Cited by 1
Unraveling transposable element-mediated regulatory landscape in diverse human immune cellsPreprint
Du, C., Fan, H., Jiang, J., Yang, J., Chen, S., Vorobyeva, N. E., Zhu, C., Mao, L., Li, C., Li, Y., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.10.24.620010 · Cited by 1
Directionality of transcriptional regulatory elementsPreprint
Chen, Y., Shah, S. R., Leung, A. K.-Y., Paramo, M. I., Cochran, K., Kundaje, A. B., Clark, A. G., Lis, J. T., & Yu, H. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.12.01.621925 · Cited by 1
Diverging transposon activity among polar bear sub-populations inhabiting different climate zonesPreprint
Godden, A. M., Rix, B. T., & Immler, S. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.12.04.626794 · Cited by 1
Luo, Y. N., Liang, Y., Wu, S., Deng, Y., Wu, W., Zhang, Z. Z., Wu, W., & Wang, L. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.02.07.636160 · Cited by 1
Expression spectrum of TE-derived transcripts in human adult tissuesPreprint
Miao, B., Luo, X., Ademovic, A., Yang, Y., Wu, T., & Zhang, B. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.03.29.646092 · Cited by 1
Hominoid-specific transposable elements rewired the expression of neural crest migration genesPreprint
Deelen, L., Mitchell, Z. H., Demurtas, M., Koulle, A., Valle, B. G. D., & Trizzino, M. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.04.04.647334 · Cited by 1
Recent Non-LTR Retrotransposon Activity Predicts Cancer Prevalence in MammalsPreprint
Fard, V. N., & Tollis, M. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.08.30.673284 · Cited by 1
Erythropoietin reshapes the adult hippocampal chromatin landscape to promote neurogenesisPreprint
Çakır, U., Fritz, M., Butt, U. J., Kawaguchi, R., Geschwind, D. H., Nave, K., Ehrenreich, H., & Singh, M. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.10.13.682070 · Cited by 1
Insertion of an invading retrovirus regulates a novel color trait in swordtail fishPreprint
Haghani, N. B., Dodge, T. O., Baczenas, J. J., Gunn, T. R., He, Q., Pangburn, W., Sood, R., Fascinetto‐Zago, P., Du, K., Kaatmann, A., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.11.07.687308 · Cited by 1
Retroviral insertions contributed to the divergence of human and chimpanzee brainsPreprint
Gerdes, P., Karlsson, O., Garza, R., Atacho, D. A. M., Hsieh, P., Prajapati, B., Muralidharan, C., Adami, A., Davis-Hansson, C., Johansson, E. M., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2025.12.12.693858 · Cited by 1
Carloni, R., Devlin, T., Tong, P., Spanos, C., Auchynnikava, T., Rappsilber, J., Matthews, K. R., & Allshire, R. C. (2026) · eLife · doi:10.7554/elife.109950 · Cited by 1
Cis-regulatory co-option of a transposon family reinforces cell identity across the immune system
Chobirko, J. D., Feschotte, C., & Grimson, A. (2026) · The EMBO Journal · doi:10.64898/2025.12.22.696042 · Cited by 1
Self-citationTracy, L., Chen, Y., & Zhang, Z. Z. (2026) · Genes & Development · doi:10.1101/gad.353011.125 · Cited by 1
Tiusanen, V., Patel, D., Xia, J., Xu, C., Datta, S., Yun, J. W., Cancellieri, S., Fei, L., Yilmaz, M., Pitkänen, E., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.01.23.701252 · Cited by 1
Retrotransposons hijack alt-EJ DNA repair process for mobilization and eccDNA biogenesisPreprint
Yang, F., Su, W., Chung, O. W., Tracy, L., Wang, L., Ramsden, D. A., & Zhang, Z. Z. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.09.25.509424
Chromosomes: Noncoding DNA (Including Satellite DNA)
Mortimer, S. M., Frisbie, T. J., Moldovan, J. B., Nakamura, M., Sandwith, S. N., Yin, J., & Moran, J. V. (2022) · Wiley eBooks · doi:10.1002/9780470015902.a0025409
Transposable element competition shapes the deer mouse genomePreprint
Gozashti, L., Feschotte, C., & Hoekstra, H. E. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.10.18.512801
Self-citationEmergence of new enhancers at late DNA replicating regionsPreprint
Cornejo‐Páramo, P., Petrova, V., Zhang, X., Young, R. S., & Wong, E. S. W. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.12.22.521323
Uneme, Y., Maeda, R., Nakayama, G., Narita, H., Takeda, N., Hiramatsu, R., Nishihara, H., Nakato, R., Kanai, Y., Araki, K., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.06.26.546627
ZMYM2 controls human transposable element transcription through distinct co-regulatory complexesPreprint
Owen, D. J., Aguilar-Martínez, E., Ji, Z., Li, Y., & Sharrocks, A. D. (2023) · eLife · doi:10.7554/elife.86669.2
Park, E. G., Lee, Y. J., Huh, J., Park, S.-J., Imai, H., Kim, W. R., Lee, D. H., Kim, J. M., Shin, H. J., & Kim, H. (2023) · Genes · doi:10.3390/genes14111984
ProA and ProB repeat sequences shape 3D genome organization in eukaryotesPreprint
Bonnet, K., Hulo, N., Mourad, R., Ewing, A. D., Croce, O., Naville, M., Vassetzky, N. S., Gilson, É., Picard, D., & Fourel, G. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.10.27.564043
ELL3 links LINE-1 to naive pluripotency of embryonic stem cells
Chang, Z., Zhu, X., Gao, S., & Gao, Y. (2023) · Chinese Science Bulletin (Chinese Version) · doi:10.1360/tb-2023-1033
Stress-induced endogenous-dsRNAs drive beta-cells to IFN-I statePreprint
Chi, K. K., Senapati, P., Leung, A., & Schones, D. E. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.11.10.566600
Crawford, B. I., Talley, M. J., Russman, J., Riddle, J., Torres, S., Williams, T., & Longworth, M. S. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.01.22.576652
Lin, J., Wu, Y., Zeng, J., Xiong, W., He, S., Pontarotti, P., & Zhu, H. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.03.04.583292
Schettini, G. P., Morozyuk, M., & Biase, F. H. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.03.15.585311
New genes are involved in the adaptation of acorn barnacles to sessile life
(2024) · Nature Genetics · doi:10.1038/s41588-024-01734-6
Epigenetic Control of Cell Fate Decisions by Enhancer-Derived Long Noncoding RNAs
Mattick, J. S. (2024) · Springer eBooks · doi:10.1007/978-3-031-59286-7_2
BMAL1 represses transposable elements independently of CLOCK in pluripotent cellsPreprint
Gallardo, A., Belmonte‐Reche, E., Marti-Marimon, M., Domingo-Reinés, J., Peris, G., López-Onieva, L., Fernández-Rengel, I., Tristán-Ramos, P., Bellora, N., Sánchez–Pozo, A., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.06.18.599568
regulaTER: An R Library to Study the Regulatory Roles of Transposable ElementsPreprint
Eskier, D., Yetkin, S., Arslan, N., Karakülah, G., & Alotaibi, H. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.06.29.601318
Zhuang, Q. K.-W., Bauermeister, K., Gálvez, J. H., AlOgayil, N., Batdorj, E., de Villena, F. P., Taketo, T., Bourque, G., & Naumova, A. K. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.09.10.612032
KTED: a comprehensive web-based database for transposable elements in the Korean genome
Lee, J., Lee, S., Lee, D.-Y., Hwang, T.-Y., Joe, S., Yang, J. O., Jeong, J., Ohn, J. H., & Kim, J. H. (2024) · Bioinformatics Advances · doi:10.1093/bioadv/vbae179
Transposable elements drive regulatory and functional innovation of F-box genesPreprint
Almeida, M. V., Li, Z., Rebelo‐Guiomar, P., Dallaire, A., Fiedler, L., Price, J. L., Sluka, J., Liu, X., Butter, F., Rödelsperger, C., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.12.17.628972
Tan, A. D. Y., Li, R., & Li, J. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.01.13.632863
Carloni, R., Devlin, T., Tong, P., Spanos, C., Auchynnikava, T., Rappsilber, J., Matthews, K. R., & Allshire, R. C. (2026) · eLife · doi:10.7554/elife.109950.2
Safeguarding spermatogenesis from retrotransposon insertions by forming ecDNAPreprint
Tracy, L., & Zhang, Z. Z. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.05.11.653319
Roles and Future Opportunities for Genomic Architecture in Understanding Repeated Evolution
Kellermeyer, R., Alvarez‐Ponce, D., Arsuaga, J., Chain, F. J. J., Dennis, M. Y., Margres, M. J., Meisel, R. P., Meyer, W. K., Moon, T. S., Smith, K. N., et al. (2025) · Integrative and Comparative Biology · doi:10.1093/icb/icaf040
Emerging Functions of the Repeat Genome in Nuclear Structure: A View from the Human Karyotype
Hall, L. L., Smith, K. P., & Lawrence, J. B. (2025) · Annual Review of Genomics and Human Genetics · doi:10.1146/annurev-genom-111522-014017
Wang, Y., Wang, W., Liu, Y., He, Y., Song, H., Yang, M., Wang, N., Wang, X., Ding, L., Kuo, Y., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.06.17.659919
Evolution of Gene Regulatory Systems
Roy, S. (2025) · Springer eBooks · doi:10.1007/978-981-96-6823-6_11
Genome Assembly, Polishing, and Analysis of the Chytrid Batrachochytrium salamandrivorans
Wacker, T., Studholme, D. J., & Farrer, R. A. (2025) · Methods in molecular biology · doi:10.1007/978-1-0716-4702-8_9
Colin, C., Lawson‐Michod, K. A., Johnson, C. E., Vlasac, I., Yoder, S., Mesa, T., Roeber, D., Huff, C. D., Hildebrandt, M. A. T., Haller, K., et al. (2025) · Clinical Epigenetics · doi:10.1186/s13148-025-01942-9
Miao, B., Zhang, Y., Shao, W., Fu, S., Bartolomei, M. S., Walker, C., Coarfa, C., Zhang, B., & Wang, T. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.07.28.667212
Ancient retrotransposon-derived promoters for mammalian genomic imprintingPreprint
Kim, J. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.07.14.664778
MLL2 facilitates long-range gene regulation through LINE1 elementsPreprint
Shahidian, L. Z., Filippo, L. D., Robert, S. M., & Rada-Iglesias, Á. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.08.10.669526
Garza, R., Adami, A., Thiruvalluvan, A., Wijesinghe, S. S., Curle, A. J., Tam, O. H., Forcier, T., Lagka, D. A., Kazakou, N.-L., Atacho, D. A. M., et al. (2026) · Science Advances · doi:10.1126/sciadv.aed2952 · Cited by 3
Bae, Y. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26189061
Modification of adipose mass by targeting distal enhancers of Ptrf
Zhang, Y. L., Long, K., Zhang, S., Zhang, B., Li, X., Li, Z., Zhong, Z., Li, P., Chen, L., Li, P., et al. (2025) · BMC Biology · doi:10.1186/s12915-025-02405-6 · Cited by 1
A new type of tandem repeats in the Mus musculus genome – GC-rich megasatellites
Nazipova, N. N., & Тетуев, Р. К. (2025) · Mathematical Biology and Bioinformatics · doi:10.17537/2025.20.416
Sáez-Vera, C., Núñez-Acuña, G., & Gallardo‐Escárate, C. (2025) · Aquaculture · doi:10.1016/j.aquaculture.2025.743270
Li, Y., Xiao, P., Boadu, F., Goldkamp, A. K., Nirgude, S., Cheng, J. J., Hagen, D. E., Kalish, J. M., & Rivera, R. M. (2025) · NAR Molecular Medicine · doi:10.1093/narmme/ugaf036 · Cited by 4
Induction of cellular totipotency by NACC1-driven feed-forward regulationPreprint
Meharwade, T., Duran-Bishop, G., Joumier, L., Dhakal, S., Usama, M., Jagdish, S., Lambert, É., Kherdjemil, Y., Robert, F., & Malleshaiah, M. K. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.10.14.682353
Gene regulatory innovations from transposable elements in mammalian cerebellum developmentPreprint
Yamada, T., Sepp, M., Sarropoulos, I., & Kaessmann, H. (2025) · bioRxiv · doi:10.1101/2025.10.15.682527
Turan, E., Çeltik, B., Dağlar, G., Kaya, İ., Tüfekçİ, M., & Yandım, C. (2025) · Journal of Biosciences · doi:10.1007/s12038-025-00562-y
Germline-limited transposon remnants foster somatic genome diversificationPreprint
Stefanov, B., & Nowacki, M. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.11.02.686105
The Impact of Transposable Elements on Immune Pathways
Salinas‐Pena, M., Homs-Aguadé, P., & Jordan, A. (2025) · Epigenetics and human health · doi:10.1007/978-3-032-04125-8_8 · Cited by 1
Transposable Elements and Gene Duplication
Makałowska, I., & Ryczek, N. (2025) · Epigenetics and human health · doi:10.1007/978-3-032-04125-8_2
The Role of Transposable Elements in Development
McCoy, J. R., & Doucet-O’Hare, T. T. (2025) · Epigenetics and human health · doi:10.1007/978-3-032-04125-8_7
Epigenetic Control of Transposable Elements
Liang, Z., Jia, C., Yao, X., & Zhang⋆, Y. (2025) · Epigenetics and human health · doi:10.1007/978-3-032-04125-8_4
Newly Evolved Endogenous Retroviruses Prime the Ovarian Reserve for ActivationPreprint
Munakata, Y., Hu, M., Dani, R. G., Inoue, N., Schultz, R. M., & Namekawa, S. H. (2025) · Research Square · doi:10.1101/2025.11.10.687753 · Cited by 1
Transposable elements in aging: From biomarkers to effectors
Fuentes-Iglesias, A., García-Vílchez, R., & Guallar, D. (2025) · Advances in genetics · doi:10.1016/bs.adgen.2025.11.001
Retrotransposons as both “architects” and “saboteurs” in the nervous system
Izquierdo‐Useros, N., Dierssen, M., Clotet, B., Elizalde‐Torrent, A., & Carriba, P. (2025) · Advances in genetics · doi:10.1016/bs.adgen.2025.11.002 · Cited by 2
Shimazaki, T., Hisamatsu, D., Naka-Kaneda, H., & Okano, H. (2025) · SSRN Electronic Journal · doi:10.2139/ssrn.5850071
Rojas, J., Castillo, H., Mundaca, M., Fraga, J., Gilbert, C., Valdebenito‐Maturana, B., & Marcellini, S. (2025) · Mobile DNA · doi:10.1186/s13100-025-00384-7 · Cited by 1
Carloni, R., Devlin, T., Tong, P., Spanos, C., Auchynnikava, T., Rappsilber, J., Matthews, K. R., & Allshire, R. C. (2025) · eLife · doi:10.7554/elife.109950.1
Cheng, K. C. L., Frost, J. M., Sanchez-Luque, F. J., García-Cañadas, M., Taylor, D., Yang, W. R., Irayanar, B., Sampath, S., Patani, H., Agger, K., et al. (2024) · DIGITAL.CSIC (Spanish National Research Council (CSIC)) · doi:10.6084/m9.figshare.26627302
Wang, C., Chen, C., Lei, B., Qin, S., Zhang, Y., Li, K., Zhang, S., & Liu, Y. (2024) · Figshare · doi:10.6084/m9.figshare.26704137
Wang, C., Chen, C., Lei, B., Qin, S., Zhang, Y., Li, K., Zhang, S., & Liu, Y. (2024) · Figshare · doi:10.6084/m9.figshare.26704146
Wang, C., Chen, C., Lei, B., Qin, S., Zhang, Y., Li, K., Zhang, S., & Liu, Y. (2024) · Figshare · doi:10.6084/m9.figshare.26704119
Wang, C., Chen, C., Lei, B., Qin, S., Zhang, Y., Li, K., Zhang, S., & Liu, Y. (2024) · Figshare · doi:10.6084/m9.figshare.26704113
Arora, A., Kolberg, J. E., Srinivasachar Badarinarayan, S., Savytska, N., Munot, D., Müller, M., Krchlíková, V., Sauter, D., & Bansal, V. (2024) · Figshare · doi:10.6084/m9.figshare.26614642
Cheng, K. C. L., Frost, J. M., Sanchez-Luque, F. J., García-Cañadas, M., Taylor, D., Yang, W. R., Irayanar, B., Sampath, S., Patani, H., Agger, K., et al. (2024) · DIGITAL.CSIC (Spanish National Research Council (CSIC)) · doi:10.6084/m9.figshare.26627296
Wang, C., Chen, C., Lei, B., Qin, S., Zhang, Y., Li, K., Zhang, S., & Liu, Y. (2024) · Figshare · doi:10.6084/m9.figshare.26704107
Wang, C., Chen, C., Lei, B., Qin, S., Zhang, Y., Li, K., Zhang, S., & Liu, Y. (2024) · Figshare · doi:10.6084/m9.figshare.26704125
Wang, C., Chen, C., Lei, B., Qin, S., Zhang, Y., Li, K., Zhang, S., & Liu, Y. (2024) · Figshare · doi:10.6084/m9.figshare.26704122
Cheng, K. C. L., Frost, J. M., Sanchez-Luque, F. J., García-Cañadas, M., Taylor, D., Yang, W. R., Irayanar, B., Sampath, S., Patani, H., Agger, K., et al. (2024) · DIGITAL.CSIC (Spanish National Research Council (CSIC)) · doi:10.6084/m9.figshare.26627293
Boyboy, B. A. G., & Ichiyanagi, K. (2024) · Figshare · doi:10.6084/m9.figshare.25801092
Wang, C., Chen, C., Lei, B., Qin, S., Zhang, Y., Li, K., Zhang, S., & Liu, Y. (2024) · Figshare · doi:10.6084/m9.figshare.25572518
Wang, C., Chen, C., Lei, B., Qin, S., Zhang, Y., Li, K., Zhang, S., & Liu, Y. (2024) · Figshare · doi:10.6084/m9.figshare.26704110
Wang, C., Chen, C., Lei, B., Qin, S., Zhang, Y., Li, K., Zhang, S., & Liu, Y. (2024) · Figshare · doi:10.6084/m9.figshare.26704134
Wang, C., Chen, C., Lei, B., Qin, S., Zhang, Y., Li, K., Zhang, S., & Liu, Y. (2024) · Figshare · doi:10.6084/m9.figshare.26704161
Arora, A., Kolberg, J. E., Srinivasachar Badarinarayan, S., Savytska, N., Munot, D., Müller, M., Krchlíková, V., Sauter, D., & Bansal, V. (2024) · Figshare · doi:10.6084/m9.figshare.26614651
Wang, C., Chen, C., Lei, B., Qin, S., Zhang, Y., Li, K., Zhang, S., & Liu, Y. (2024) · Figshare · doi:10.6084/m9.figshare.26704143
Wang, C., Chen, C., Lei, B., Qin, S., Zhang, Y., Li, K., Zhang, S., & Liu, Y. (2024) · Figshare · doi:10.6084/m9.figshare.26704149
Wang, C., Chen, C., Lei, B., Qin, S., Zhang, Y., Li, K., Zhang, S., & Liu, Y. (2024) · Figshare · doi:10.6084/m9.figshare.26704128
Boyboy, B. A. G., & Ichiyanagi, K. (2024) · Figshare · doi:10.6084/m9.figshare.25800965
Additional file 2 of Asymmetric and parallel subgenome selection co-shape common carp domestication
Wang, M., Li, X., Wang, C., Zou, M., Yang, J., Li, X.-D., & Guo, B. (2024) · Figshare · doi:10.6084/m9.figshare.24934706
Cheng, K. C. L., Frost, J. M., Sanchez-Luque, F. J., García-Cañadas, M., Taylor, D., Yang, W. R., Irayanar, B., Sampath, S., Patani, H., Agger, K., et al. (2024) · DIGITAL.CSIC (Spanish National Research Council (CSIC)) · doi:10.6084/m9.figshare.24320052
Wang, C., Chen, C., Lei, B., Qin, S., Zhang, Y., Li, K., Zhang, S., & Liu, Y. (2024) · Figshare · doi:10.6084/m9.figshare.26704158
Cheng, K. C. L., Frost, J. M., Sanchez-Luque, F. J., García-Cañadas, M., Taylor, D., Yang, W. R., Irayanar, B., Sampath, S., Patani, H., Agger, K., et al. (2024) · Figshare · doi:10.6084/m9.figshare.26627299
Wang, C., Chen, C., Lei, B., Qin, S., Zhang, Y., Li, K., Zhang, S., & Liu, Y. (2024) · Figshare · doi:10.6084/m9.figshare.25572650
Wang, C., Chen, C., Lei, B., Qin, S., Zhang, Y., Li, K., Zhang, S., & Liu, Y. (2024) · Figshare · doi:10.6084/m9.figshare.26704116
Cheng, K. C. L., Frost, J. M., Sanchez-Luque, F. J., García-Cañadas, M., Taylor, D., Yang, W. R., Irayanar, B., Sampath, S., Patani, H., Agger, K., et al. (2023) · Figshare · doi:10.6084/m9.figshare.24319923
Wang, C., Chen, C., Lei, B., Qin, S., Zhang, Y., Li, K., Zhang, S., & Liu, Y. (2024) · Figshare · doi:10.6084/m9.figshare.26704140
Metadata
- Authors
- Fueyo, R., Judd, J., Feschotte, C., & Wysocka, J.
- Affiliations
- Stanford Medicine (US)
- Cornell University (US)
- Howard Hughes Medical Institute (US)
- Corresponding author
- Wysocka, Joanna
- Venue
- Nature Reviews Molecular Cell Biology
- Published
- 2022-02-28
- Volume
- 23
- Issue
- 7
- Pages
- 481-497
- ISSN
- 1471-0072 (ISSN-L)
- 1471-0080
- PMC
- PMC10470143
- OpenAlex
- W4214672693
- Cited by
- 451
- References
- 226
- Citations by year
- 2026: 80 · 2025: 139 · 2024: 119 · 2023: 89 · 2022: 24
- FWCI
- 9.07
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Nature Reviews Molecular Cell Biology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Howard Hughes Medical Institute
- Cancer Research Institute
- Bristol-Myers Squibb
- National Institutes of Health
- National Human Genome Research Institute (U01HG009391, F31HG010820)
- National Cancer Institute (R01CA260691)
- National Institute of General Medical Sciences (R35GM122550, R35GM131757)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Chromosomal and Genetic Variations
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genomic variations and chromosomal abnormalities
- Keywords
- transposable elements, transcriptional regulation, mammalian genomes, cis-regulatory elements, enhancers, promoter, 3D genome organization, non-coding RNA, transcription factors, regulatory evolution, genetic novelty, genomic context, repetitive DNA
- MeSH terms
- Animals, DNA Transposable Elements, Gene Expression Regulation, Mammals, Promoter Regions, Genetic, Regulatory Sequences, Nucleic Acid, Transcription Factors, Evolution, Molecular
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