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 201–300 of 475
de Oliveira, F. S., Brann, T., Wolf, I. R., Nogaroto, V., Martins, C., Protasio, A. V., & Vicari, M. R. (2025) · Chromosome Research · doi:10.1007/s10577-025-09765-3 · Cited by 4
Transposable Elements Drive Regulatory and Functional Innovation of F-box Genes
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. (2025) · Molecular Biology and Evolution · doi:10.1093/molbev/msaf097 · Cited by 5
Wang, H., Chen, X., Li, Y., Xiao, S., Teng, T., Yang, S., Wang, K., & Zhang, M. (2025) · Non-coding RNA Research · doi:10.1016/j.ncrna.2025.08.006 · Cited by 4
Transposable elements drive evolution and perturb gene expression in Brassica rapa and B. oleracea
Zheng, P., Ko, C., Ou, J., Zuccolo, A., & Lin, Y. (2025) · The Plant Journal · doi:10.1111/tpj.70452 · Cited by 5
Population genetic analysis based on the polymorphisms mediated by transposons in the genomes of pig
Zong, W., Zhao, R., Wang, X., Zhou, C., Wang, J., Chen, C., Niu, N., Zheng, Y., Chen, L., Liu, X., et al. (2024) · DNA Research · doi:10.1093/dnares/dsae008 · Cited by 5
Structural and biochemical studies of mobile retrotransposon proteins in action
Thawani, A., Collins, K., & Nogales, E. (2025) · Current Opinion in Structural Biology · doi:10.1016/j.sbi.2025.103053 · Cited by 5
Hamann, M. V., Adiba, M., & Lange, U. C. (2023) · BMC Medical Genomics · doi:10.1186/s12920-023-01486-y · Cited by 4
Fukuda, K. (2023) · Genes & Genetic Systems · doi:10.1266/ggs.23-00140 · Cited by 5
Stévant, I., Gonen, N., & Poulat, F. (2024) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1327410 · Cited by 4
Crawford, B. I., Talley, M. J., Russman, J., Riddle, J., Torres, S., Williams, T., & Longworth, M. S. (2024) · Nature Communications · doi:10.1038/s41467-024-47042-9 · Cited by 5
Insertion of short L1 sequences generates inter-strain histone acetylation differences in the mouse
Boyboy, B. A. G., & Ichiyanagi, K. (2024) · Mobile DNA · doi:10.1186/s13100-024-00321-0 · Cited by 4
Li, Y., Xiao, P., Boadu, F., Goldkamp, A. K., Nirgude, S., Cheng, J. J., Hagen, D. E., Kalish, J. M., & Rivera, R. M. (2023) · medRxiv · doi:10.1101/2023.12.14.23299981 · Cited by 4
Transcriptional perturbation of LINE-1 elements reveals their cis -regulatory potentialPreprint
Perez-Rico, Y. A., Bousard, A., Misikova, L. H., Mulugeta, E., de Almeida, S. F., Muotri, A. R., Heard, É., & Gendrel, A.-V. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.02.20.581275 · Cited by 4
What would it take to prove that a chronic infection is a causal agent in Alzheimer’s disease?
Brutkiewicz, R. R., Cao, W., Morgan, D., Reis, R. S. D., Suryadevara, V., Willette, A. A., Willette, S. A., Wyatt-Johnson, S. K., & Duggan, M. R. (2025) · Trends in Neurosciences · doi:10.1016/j.tins.2025.05.009 · Cited by 3
Hominoid-specific transposable elements reshaped neural crest migration in craniofacial development
Deelen, L., Mitchell, Z. H., Demurtas, M., Koulle, A., Valle, B. G. D., & Trizzino, M. (2025) · Molecular Systems Biology · doi:10.1038/s44320-025-00151-z · Cited by 5
Jiao, Z., Mukiibi, R., Gundappa, M. K., Babbucci, M., Prendergast, J. G. D., Robledo, D., Bargelloni, L., & Macqueen, D. J. (2025) · BMC Biology · doi:10.1186/s12915-025-02404-7 · Cited by 4
You, J. S., Pierce, S., Liang, G., & Jones, P. A. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2502963122 · Cited by 6
panHiTE: A comprehensive and accurate pipeline for TE detection in large-scale population genomes
Hu, K., Xu, M., Ding, L., Zou, Y. F., Gao, X., & Wang, J. (2025) · Plant Communications · doi:10.1016/j.xplc.2025.101669 · Cited by 4
Double stranded RNA sensing is silenced during early embryonic development
Witteveldt, J., Liu, Z., Ariza‐Cosano, A., Ramirez, C., Walters, J. L. H., Marchante, P. G., van der Maas, L. N., Friman, E. T., Ivens, A. C., Tebaldi, T., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-66352-0 · Cited by 3
Transposons disrupt genomic stability and trigger cancers
Dong, W., Li, M., Li, P., Hou, X. S., He, F., & Ji, S. (2025) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2025.1704405 · Cited by 3
Transposable elements as drivers of genome evolution in Drosophila virilis
Rezvykh, A. P., Kulikova, D. A., Zelentsova, E. S., Protsenko, L., Bespalova, A. V., Guseva, I. O., Blumenstiel, J. P., Евгеньев, М. Б., & Funikov, S. Y. (2026) · Nucleic Acids Research · doi:10.1093/nar/gkag139 · Cited by 4
Chen, C., Du, Z., Zheng, Y., Chen, H., Saleh, A. A., Yang, N., Wang, M., Azele, P., Wang, X., & Song, C. (2024) · Viruses · doi:10.3390/v16111801 · Cited by 3
The nuclear exosome co-factor MTR4 shapes the transcriptome for meiotic initiation
Zhang, L., Wang, J., Tang, Z., Lin, Z., Su, R., Hu, N., Tang, Y., Ge, G., Fan, J., Tong, M., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-57898-0 · Cited by 5
Ruiz‐Pérez, S., Alcaraz, N., Torres‐Arciga, K., Ocampo‐Cervantes, J. A., Cervera, A., Hernández, C. C., Sámano, C., Soto‐Reyes, E., & González‐Barrios, R. (2025) · Advanced Biology · doi:10.1002/adbi.202400502 · Cited by 3
Sano, R., Fukuda, H., Kubo, R., Oishi, T., Miyabe‐Nishiwaki, T., Kaneko, A., Masato, H., Takahashi, Y., Hayakawa, A., Yazawa, S., et al. (2023) · Scientific Reports · doi:10.1038/s41598-023-31961-6 · Cited by 3
Deaville, L. A., & Berrens, R. V. (2024) · Biochemical Society Transactions · doi:10.1042/bst20231262 · Cited by 3
Inter-chromosomal insertions into wild-type chromosomes induced by SCRaMbLE
Zhou, S., Li, J., Cui, X., Wang, Y., & Yuan, Y. (2024) · Frontiers of Chemical Science and Engineering · doi:10.1007/s11705-024-2458-5 · Cited by 3
The silent guardian: unraveling the roles of H3K9me3 in genome maintenance
Li, Z., & Zhang, Z. (2024) · Genome Instability & Disease · doi:10.1007/s42764-024-00131-x · Cited by 3
Schettini, G. P., Morozyuk, M., & Biase, F. H. (2024) · BMC Genomics · doi:10.1186/s12864-024-10685-5 · Cited by 3
Transposable element activity captures human pluripotent cell states
Levin-Ferreyra, F., Kodali, S., Cui, Y., Swearingen, A. R., Pessina, P., Brumbaugh, J., & Stefano, B. D. (2024) · EMBO Reports · doi:10.1038/s44319-024-00343-y · Cited by 4
Near-chromosome level genome assembly of devil firefish, Pterois miles
Kitsoulis, C. V., Papadogiannis, V., Kristoffersen, J. B., Kaitetzidou, E., Sterioti, A., Tsigenopoulos, C. S., & Manousaki, T. (2023) · Peer Community Journal · doi:10.24072/pcjournal.295 · Cited by 3
Comprehensive Hierarchical Classification of Transposable Elements based on Deep LearningPreprint
Qi, Y., Chen, Y., Wu, Y., Li, Y., Gao, M., Zhang, F., Liao, X., & Shang, X. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.01.27.577599 · Cited by 3
Germline ecology: Managed herds, tolerated flocks, and pest control
Haig, D. (2024) · Journal of Heredity · doi:10.1093/jhered/esae004 · Cited by 2
Human lncRNAs harbor conserved modules embedded in different sequence contexts
Ballesio, F., Pepe, G., Ausiello, G., Novelletto, A., Helmer‐Citterich, M., & Gherardini, P. F. (2024) · Non-coding RNA Research · doi:10.1016/j.ncrna.2024.06.013 · Cited by 2
Hu, J., Gui, L., Wu, Z., & Huang, L. (2024) · Journal of Animal Science and Biotechnology/Journal of animal science and biotechnology · doi:10.1186/s40104-024-01121-5 · Cited by 2
Pogo transposons provide tools to restrict cancer growth
Zueva, E., & Burbage, M. (2025) · Molecular Oncology · doi:10.1002/1878-0261.13801 · Cited by 2
Zhuang, Q. K.-W., Bauermeister, K., Gálvez, J. H., AlOgayil, N., Batdorj, E., de Villena, F. P., Taketo, T., Bourque, G., & Naumova, A. K. (2025) · Genome biology · doi:10.1186/s13059-025-03547-0 · Cited by 2
Biomolecular liquid‒liquid phase separation associated with repetitive genomic elements
Asamitsu, S., & Iwasaki, Y. W. (2025) · Polymer Journal · doi:10.1038/s41428-025-01036-6 · Cited by 3
Behm, R., & Sharanowski, B. J. (2025) · Mobile DNA · doi:10.1186/s13100-025-00360-1 · Cited by 2
DDX55 safeguards naïve T cell homeostasis by suppressing activation-promoting transposable elements
Wu, M., Linghu, K., Yin, Q.-S., He, P., Yu, X., Hu, P., He, R., Du, Q., Wang, S., Chen, X. X., et al. (2025) · Science Immunology · doi:10.1126/sciimmunol.adq0457 · Cited by 2
Serebrovska, Z. O., Xi, L., Khetsuriani, M., Protsenko, O. V., Morozova, N., Tolstun, D. A., & Maksymchuk, O. (2025) · Brain Research · doi:10.1016/j.brainres.2025.149953 · Cited by 2
Arteaga-Vazquez, L. J., Sepúlveda, H., Reveles, B. V., Suzuki, K., KALUNIAN, K. C., Ay, F., Boothby, M. R., & Rao, A. (2025) · Mobile DNA · doi:10.1186/s13100-025-00377-6 · Cited by 5
Transcriptional regulation of human NMNAT2 : insights from 3D genome sequencing and bioinformatics
Chang, Y. C., Yang, S., Cho, M., Nho, K. T., Baizabal, J., & Lu, H. (2025) · FEBS Journal · doi:10.1111/febs.70322 · Cited by 4
Molecular effects of transposable element sequences in mammalian cells
Wen, M., & Welch, J. D. (2025) · Genome biology · doi:10.1186/s13059-025-03883-1 · Cited by 2
Major waves of H2A.Z incorporation during mouse oogenesis and preimplantation embryo development
Fosslie, M., Ilaslan, E., Skuland, T., Choudalakis, M., Soegaard, M. D., Halliwell, J. A., Khan, S., Indahl, M., Vera-Rodríguez, M., Manaf, A., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-66919-x · Cited by 2
Nakakita, B., Mizuta, K., Katou, Y., Tasaki, H., Nakamura, T., Yabuta, Y., Iwatani, C., Tsuchiya, H., Kawamoto, I., Tsukiyama, T., et al. (2026) · Development · doi:10.1242/dev.205241 · Cited by 2
Expression spectrum of TE-driven transcripts in human adult tissues
Miao, B., Luo, X., Ademovic, A., Yang, Y., Wu, T. P., & Zhang, B. A. (2026) · Genome biology · doi:10.1186/s13059-025-03898-8 · Cited by 3
Nishihara, H., & Komiya, A. (2026) · Genome biology · doi:10.1186/s13059-026-04050-w · Cited by 2
Wang, L., Liang, Y., Wu, S., Deng, Y., Wu, W., Zhang, Z. Z. Z., Wu, W., & Wang, L. (2026) · Molecular Cell · doi:10.1016/j.molcel.2026.05.022 · Cited by 3
Matoba, N., McAfee, J. C., Krupa, O., Beltran, A. A., Bell, J., Le, B. D., Valone, J. M., Min, H.-G., Crawford, G. E., Raab, J. R., et al. (2026) · Nature Neuroscience · doi:10.1038/s41593-026-02454-2 · Cited by 5
ZMYM2 controls human transposable element transcription through distinct co-regulatory complexes
Owen, D. J., Aguilar-Martínez, E., Ji, Z., Li, Y., & Sharrocks, A. D. (2023) · eLife · doi:10.7554/elife.86669.3 · Cited by 2
Retrotransposons and Diabetes Mellitus
Katsanou, A., Kostoulas, C., Liberopoulos, E. N., Tsatsoulis, A. A., Georgiou, I. A., & Tigas, S. K. (2024) · Epigenomes · doi:10.3390/epigenomes8030035 · Cited by 4
Ferreira, G. R., Emond-Rhéault, J.-G., Alves, L. R., Leprohon, P., Smith, M. A., & Papadopoulou, B. (2024) · BMC Biology · doi:10.1186/s12915-024-02051-4 · Cited by 2
Eskier, D., Yetkin, S., Arslan, N., Karakülah, G., & Alotaibi, H. (2024) · Journal of Molecular Biology · doi:10.1016/j.jmb.2024.168887 · Cited by 2
Core factor of NEXT complex, ZCCHC8, governs the silencing of LINE1 during spermatogenesis
Yan, R., Qi, M., Zhang, P., Shen, B., Yin, J., Chen, C., Tian, S., Chen, L., Huang, X., Wang, H., et al. (2024) · National Science Review · doi:10.1093/nsr/nwae407 · Cited by 2
PIF/harbinger transposon-derived protein promotes 7SL expression to enhance pathogen resistance
Geng, S., Lv, X., & Xu, T. (2025) · EMBO Reports · doi:10.1038/s44319-025-00379-8 · Cited by 2
A plan or pandemonium? The conundrum of retrotransposon activation in cancer
Zueva, E. (2025) · Mobile DNA · doi:10.1186/s13100-025-00368-7 · Cited by 3
Souaifan, H., Costallat, M., Sitkiewicz, L., Godest, K., Cammas, F. M., Mann, C., Muchardt, C., & Rachez, C. (2026) · Nature Communications · doi:10.1038/s41467-026-72504-7 · Cited by 2
Lee, D. H., Park, E. G., Kim, J.-M., Shin, H. J., Lee, Y. J., Jeong, H.-S., Roh, H.-Y., Kim, W. R., Ha, H., Kim, S.-W., et al. (2024) · Genes & Genomics · doi:10.1007/s13258-024-01547-1 · Cited by 3
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) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.01.24.525372 · Cited by 2
Wang, K., Hua, G., Li, J., Yu, Y., Zhang, C., Yang, L., Hu, X., Scheben, A., Wu, Y., Gong, P., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.01.28.526061 · Cited by 2
ZMYM2 controls 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.86669.1 · Cited by 2
Cryptic endogenous retrovirus subfamilies in the primate lineagePreprint
Chen, X., Zhang, Z., Yan, Y.-Z., Goubert, C., Bourque, G., & Inoue, F. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.12.07.570592 · Cited by 2
Barai, P., Biswas, S. K., Verma, P., & Duncan, E. M. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.07.20.604429 · Cited by 2
Fagundes, W. C., Möller, M., Feurtey, A., Hansen, R., Haueisen, J., Salimi, F., Alizadeh, A., & Stukenbrock, E. H. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.10.03.616481 · Cited by 2
Zinc-finger proteins with a co-opted capsid domain anchor nucleosomes over transposon sequencesPreprint
Matsushima, W., Duc, J., Sheppard, S., Pulver, C., Grün, D., Offner, S., Raclot, C., Planet, E., & Trono, D. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.03.03.638093 · Cited by 2
Double stranded RNA sensing drives interferon silencing in early developmentPreprint
Witteveldt, J., Liu, Z., Ariza‐Cosano, A., Ramirez, C., Walters, J. L. H., Marchante, P. G., van der Maas, L. N., Ivens, A. C., Tebaldi, T., Heras, S. R., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.03.10.642424 · Cited by 2
Zheng, Y., Yang, N., Chen, C., Zong, W., Chen, H., Shi, S., Wang, X., Muráni, E., Reyer, H., Gao, B., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.05.21.653756 · Cited by 2
Arteaga-Vazquez, L. J., Sepúlveda, H., Reveles, B. V., Suzuki, K., KALUNIAN, K. C., Ay, F., Boothby, M. R., & Rao, A. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.05.30.657099 · Cited by 2
Transposons as Environmental Stress Detectors, Are Eukaryotic Genomes Evolved to Evolve?
Hunter, R. G. (2024) · Springer eBooks · doi:10.1007/978-3-031-59286-7_13 · Cited by 1
Baptista, H. S., Portela, L. M. F., Fioretto, M. N., Mattos, R., Ribeiro, I. T., Lorente, A. B. L., Oliveira, J. I. N., & Justulin, L. A. (2024) · Scientific Reports · doi:10.1038/s41598-024-77901-w · Cited by 1
Navigating a Fine Balance: Point-Mutant Cheater Viruses Disrupt the Viral Replication Cycle
Meir, M., Kahn, A., Farage, C., Maoz, Y., Harel, N., Zvi, A. B., Segev, S., Volkov, M., Yahud, R., Gophna, U., et al. (2024) · Molecular Biology and Evolution · doi:10.1093/molbev/msae258 · Cited by 1
Yang, Z., Guo, Z., Qin, B., Zhang, H., Chen, J., Zheng, G.-D., & Zou, S. (2025) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2025.110206 · Cited by 1
Expression of LTR and LINE1 transposable elements defines atypical teratoid/rhabdoid tumor subtypes
Hamann, M. V., Godbole, S., Adiba, M., Leddy, S. M., Navolić, J., Tabatabai, G., Merk, D. J., Lange, U. C., & Neumann, J. E. (2025) · Acta Neuropathologica Communications · doi:10.1186/s40478-025-02078-w · Cited by 2
Lim, C., An, H., & Park, J. (2025) · Genomics & Informatics · doi:10.1186/s44342-025-00048-1 · Cited by 1
Shen, Y., Li, L., Ni, H., Li, H., Xu, M., Tan, X., Li, Z., Li, P., Chen, F., Mao, S., et al. (2025) · Nucleic Acids Research · doi:10.1093/nar/gkaf797 · Cited by 1
Analysis of human endogenous retrovirus in hepatocellular carcinomas using HERV-Fcount
Chang, Y., Hsu, M.-H., Chung, C., Lai, I., Lee, Y.-T., Yen, J.-C., Chang, C., Liu, T., & Chang, J. (2025) · BMC Microbiology · doi:10.1186/s12866-025-04358-w · Cited by 1
Zhang, M., Wang, X., Liu, Y., Bao, C., Gao, Q., & Mao, L. (2025) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2025.1677212 · Cited by 1
Epigenetic lockdown of type I interferon sensing and signalling in human pluripotent cells
Holt, J. H., Enriquez-Gasca, R., Wilson, R. P., Bochukova, E. G., Maillard, P. V., & Rowe, H. M. (2026) · Nature Communications · doi:10.1038/s41467-026-74147-0 · Cited by 2
Structural heterogeneity and functional convergence of transposable elements
Kosovsky, G. Y., Glazko, G. V., & Glazko, T. T. (2025) · Frontiers in Genetics · doi:10.3389/fgene.2025.1605675 · Cited by 1
Transposable Elements and Genome Evolution in Vertebrates
Fard, V. N., & Tollis, M. (2025) · Epigenetics and human health · doi:10.1007/978-3-032-04125-8_1 · Cited by 1
Shi, P., Jin, K., Yin, G., & Liu, L. (2026) · Stem Cell Reports · doi:10.1016/j.stemcr.2026.102824 · Cited by 1
Host-transposon mutualism supports regeneration in planarians
Lee, H.-L., Poulet, A., Parambil, S. A., & van Wolfswinkel, J. C. (2026) · Developmental Cell · doi:10.1016/j.devcel.2026.03.001 · Cited by 1
Host-transposable element coexistence: a matter of resistance, tolerance and trade-off
Chambeyron, S., Pélisson, A., Koga, Y., Grimaud, C., & Siomi, M. C. (2026) · The EMBO Journal · doi:10.1038/s44318-026-00795-z · Cited by 2
New genomic and transposable element annotation of the microsporidian parasite Anncaliia algerae
Akossi, R. F., Rochette, L., Lerat, E., Alaoui, H. E., Courtine, D., Tournayre, J., Delbac, F., Peyretaillade, É., & Wawrzyniak, I. (2026) · Genomics · doi:10.1016/j.ygeno.2026.111322 · Cited by 1
Zhang, T., Li, X., Zhou, W., Zhao-lu, L., Bi, J., Ma, X., Li, X., Fan, Y., Hong, Y., Wang, S., et al. (2026) · Cell · doi:10.1016/j.cell.2026.07.006 · Cited by 1
The role of transposable elements-endogenous retroviruses in embryonic development and regeneration
Li, Z., Huang, Y., Ju, Z., Le, R., & Chen, Z. (2026) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2026.102517 · Cited by 2
Endogenous retrovirus control of calbindin is essential for human early embryogenesis
Pape, J., McCarthy, A., Serna-Morales, E., Gharibi, B., Plowman, T., Copin, E., Thompson, R., Doglio, L. E., Meleckyte, R., Healy, L. E., et al. (2026) · Science Advances · doi:10.1126/sciadv.aee4523 · Cited by 1
Endogenous retroviruses control human placental gene expression
Branco, M., & Frost, J. (2023) · Nature Structural & Molecular Biology · doi:10.1038/s41594-023-00965-1 · Cited by 1
Retrotransposons and telomeres
Kalmykova, A. I., & Sokolova, O. A. (2023) · Biochemistry (Moscow) · doi:10.31857/s0320972523110076 · Cited by 1
Associated technologies for genome editing
Li, K., Mu, Y., Wang, B., Ju, H., Zhou, R., Liu, Z., Wu, T., Song, C., Zhang, Y., & Xie, T. (2024) · Elsevier eBooks · doi:10.1016/b978-0-12-819099-9.00005-4 · Cited by 1
Majid, M., Liu, X., Khan, H., & Huang, Y. (2024) · Gene · doi:10.1016/j.gene.2024.149090 · Cited by 1
Transposon expression and repression in skeletal muscle
Borok, M. J., Zaidan, L. R., & Relaix, F. (2025) · Mobile DNA · doi:10.1186/s13100-025-00352-1 · Cited by 1
The Xenopus model as a tool for investigating craniofacial developmental disorders
Kong, Q., Peng, H., Zhao, Q., Jiang, H., & Zhu, X. (2025) · Frontiers in Medicine · doi:10.3389/fmed.2025.1671687 · Cited by 2
Pathway to Independence: a forecast for the future of developmental biology
Ewe, C. K., Farnworth, M. S., Miller, A., Acedo, J. N., Oomen, M. E., Paci, G., Widen, S. A., & Yamada, T. (2025) · Development · doi:10.1242/dev.205224 · Cited by 1
A histone H2A and H2B point mutant library defines essential in vivo functions in Drosophila
Sun, A., Guo, Y., Wei, Z., Zheng, J., Zhang, X., & Gao, G. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.116692 · Cited by 1
Inferring Protein-DNA Binding Profiles at Interspersed Repeats Using HiChIP and PAtChER
Taylor, D., & Branco, M. R. (2022) · Methods in molecular biology · doi:10.1007/978-1-0716-2883-6_11 · Cited by 1
Wang, L., Taylor, T., Rathnakumar, K., Khyzha, N., Liang, M., Alizada, A., Campitelli, L., Pour, S. E., Patel, Z. M., Antounians, L., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.10.25.513724 · Cited by 2
Nguyen, L. L., Watson, Z. L., Ortega, R., Woodruff, E. R., Jordan, K. R., Iwanaga, R., Yamamoto, T. M., Bailey, C. A., Jeong, A. D., Guntupalli, S. R., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.02.23.529773 · Cited by 1
ADNP Modulates SINE B2-Derived CTCF-Binding Sites during Blastocyst Formation in MousePreprint
Wang, W., Gao, R., Yang, D., Ma, M., Zang, R., Wang, X., Chen, C., Chen, J., Kou, X., Zhao, Y., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.11.24.567719 · Cited by 1
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