The DOI matches its Crossref record; 24 of the 24 references it cites were found in a registry or an index.
Activation of transposable elements during aging and neuronal decline in Drosophila
Open accessAbstract
We found that several transposable elements were highly active in Drosophila brain during normal aging. In addition, we found that mutations in Drosophila Argonaute 2 (Ago2) resulted in exacerbated transposon expression in the brain, progressive and age-dependent memory impairment, and shortened lifespan. These findings suggest that transposon activation may contribute to age-dependent loss of neuronal function.
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 source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“DNA damage-mediated cell death104 might thus be a predominant cause of deleterious effects exerted by retrotransposons in flies.”
From The role of retrotransposable elements in ageing and age-associated diseases (2021) · cites this paper as [104]
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“Sample sizes are similar to or greater than those reported in previous publications4,5,10.”
From Pathogenic tau-induced piRNA depletion promotes neuronal death through transposable element dysregulation in neurodegenerative tauopathies (2018) · cites this paper as [4]
In the citing paper
“studies in yeast, flies and mammals have noted an age-associated increase in the activation of transposable elements, contributing to genomic instability49–51.”
From Stem cell aging: mechanisms, regulators and therapeutic opportunities (2014) · cites this paper as [50]
In the citing paper
“with aging, the efficacy of these systems is known to be reduced, providing a genomic environment in which TEs may become activated and contribute to somatic mutagenesis [244, 245]”
From Genetic architecture of Alzheimer's disease (2020) · cites this paper as [245]
In the citing paper
“Neuropathologies such as tau have been observed to promote activation of TEs”
From Genetic architecture of Alzheimer's disease (2020) · cites this paper as [245]
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
Somatic mosaicism in neuronal precursor cells mediated by L1 retrotransposition
Muotri, A. R., Chu, V. T., Marchetto, M. C. N., Deng, W., Moran, J. V., & Gage, F. H. (2005) · Nature · doi:10.1038/nature03663 · Cited by 942
Genetic dissection of consolidated memory in Drosophila
Tully, T., Preat, T., Boynton, S. C., & Del Vecchio, M. (1994) · Cell · doi:10.1016/0092-8674(94)90398-0 · Cited by 924
L1 retrotransposition in human neural progenitor cells
Coufal, N. G., Garcia-Perez, J. L., Peng, G. E., Yeo, G. W., Mu, Y., Lovci, M. T., Morell, M., O’Shea, K. S., Moran, J. V., & Gage, F. H. (2009) · Nature · doi:10.1038/nature08248 · Cited by 814
Somatic retrotransposition alters the genetic landscape of the human brain
Baillie, J. K., Barnett, M. W., Upton, K. R., Gerhardt, D. J., Richmond, T. A., De Sapio, F., Brennan, P. M., Rizzu, P., Smith, S., Fell, M., et al. (2011) · Nature · doi:10.1038/nature10531 · Cited by 684
Retrotransposons Revisited: The Restraint and Rehabilitation of Parasites
Goodier, J. L., & Kazazian, H. H. (2008) · Cell · doi:10.1016/j.cell.2008.09.022 · Cited by 659
L1 retrotransposition in neurons is modulated by MeCP2
Muotri, A. R., Marchetto, M. C. N., Coufal, N. G., Oefner, R., Yeo, G., Nakashima, K., & Gage, F. H. (2010) · Nature · doi:10.1038/nature09544 · Cited by 626
Small RNA sorting: matchmaking for Argonautes
Czech, B., & Hannon, G. J. (2011) · Nature Reviews Genetics · doi:10.1038/nrg2916 · Cited by 605
DICER1 deficit induces Alu RNA toxicity in age-related macular degeneration
Kaneko, H., Dridi, S., Tarallo, V., Gelfand, B. D., Fowler, B. J., Cho, W. G., Kleinman, M. E., Ponicsan, S. L., Hauswirth, W. W., Chiodo, V. A., et al. (2011) · Nature · doi:10.1038/nature09830 · Cited by 601
The microRNA miR-34 modulates ageing and neurodegeneration in Drosophila
Liu, N., Landreh, M., Cao, K., Abe, M., Hendriks, G.-J., Kennerdell, J. R., Zhu, Y., Wang, L.-S., & Bonini, N. M. (2012) · Nature · doi:10.1038/nature10810 · Cited by 356
Douville, R. N., Liu, J., Rothstein, J., & Nath, A. (2010) · Annals of Neurology · doi:10.1002/ana.22149 · Cited by 327
Cited by
Sorted by citations
Regulatory activities of transposable elements: from conflicts to benefits
Chuong, E. B., Elde, N. C., & Feschotte, C. (2017) · Nature Reviews Genetics · doi:10.1038/nrg.2016.139 · Cited by 1,489
Pal, S., & Tyler, J. K. (2016) · Science Advances · doi:10.1126/sciadv.1600584 · Cited by 860
Stem cell aging: mechanisms, regulators and therapeutic opportunities
Oh, J., Lee, Y. D., & Wagers, A. J. (2014) · Nature Medicine · doi:10.1038/nm.3651 · Cited by 796
Jin, Y., Tam, O. H., Paniagua, E., & Hammell, M. (2015) · Bioinformatics · doi:10.1093/bioinformatics/btv422 · Cited by 753
Epigenetic regulation of ageing: linking environmental inputs to genomic stability
Benayoun, B. A., Pollina, E. A., & Brunet, A. (2015) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm4048 · Cited by 610
Booth, L. N., & Brunet, A. (2016) · Molecular Cell · doi:10.1016/j.molcel.2016.05.013 · Cited by 499
Restricting retrotransposons: a review
Goodier, J. L. (2016) · Mobile DNA · doi:10.1186/s13100-016-0070-z · Cited by 436
The role of retrotransposable elements in ageing and age-associated diseases
Gorbunova, V., Seluanov, A., Mita, P., McKerrow, W., Fenyö, D., Boeke, J. D., Linker, S. B., Gage, F. H., Kreiling, J. A., Petrashen, A. P., et al. (2021) · Nature · doi:10.1038/s41586-021-03542-y · Cited by 446
Resurrection of endogenous retroviruses during aging reinforces senescence
Liu, X., Liu, Z., Wu, Z., Ren, J., Fan, Y., Sun, L., Cao, G., Niu, Y., Zhang, B., Ji, Q., et al. (2023) · Cell · doi:10.1016/j.cell.2022.12.017 · Cited by 390
Self-citationTransposable elements become active and mobile in the genomes of aging mammalian somatic tissues
De Cecco, M., Criscione, S. W., Peterson, A. L., Neretti, N., Sedivy, J. M., & Kreiling, J. A. (2013) · Aging · doi:10.18632/aging.100621 · Cited by 365
Ubiquitous L1 Mosaicism in Hippocampal Neurons
Upton, K. R., Gerhardt, D. J., Jesuadian, J. S., Richardson, S. R., Sánchez-Luque, F. J., Bodea, G. O., Ewing, A. D., Salvador-Palomeque, C., van der Knaap, M. S., Brennan, P. M., et al. (2015) · Cell · doi:10.1016/j.cell.2015.03.026 · Cited by 320
The Influence of LINE-1 and SINE Retrotransposons on Mammalian Genomes
Richardson, S. R., Doucet, A. J., Kopera, H. C., Moldovan, J. B., Garcia-Perez, J. L., & Moran, J. V. (2015) · Microbiology Spectrum · doi:10.1128/microbiolspec.mdna3-0061-2014 · Cited by 338
Tau Activates Transposable Elements in Alzheimer’s Disease
Guo, C., Jeong, H.-H., Hsieh, Y.-C., Klein, H.-U., Bennett, D. A., De Jager, P. L., Liu, Z., & Shulman, J. M. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.05.004 · Cited by 315
Sun, W., Samimi, H., Gamez, M., Zare, H., & Frost, B. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0194-1 · Cited by 300
Cytoplasmic DNA: sources, sensing, and role in aging and disease
Miller, K. N., Victorelli, S. G., Salmonowicz, H., Dasgupta, N., Liu, T., Passos, J. F., & Adams, P. D. (2021) · Cell · doi:10.1016/j.cell.2021.09.034 · Cited by 288
Mobile DNA elements in the generation of diversity and complexity in the brain
Erwin, J. A., Marchetto, M. C., & Gage, F. H. (2014) · Nature reviews. Neuroscience · doi:10.1038/nrn3730 · Cited by 277
Loss of Nuclear TDP-43 Is Associated with Decondensation of LINE Retrotransposons
Liu, E. Y., Russ, J., Cali, C. P., Phan, J. M., Amlie-Wolf, A., & Lee, E. B. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.04.003 · Cited by 231
“Furthermore, activation of transposable elements has been observed in an age-dependent fashion in Drosophila brain, contributing to memory decline and mortality (Li et al., 2013).”
BackgroundPetersen, M., Armisén, D., Gibbs, R. A., Hering, L., Khila, A., Mayer, G., Richards, S., Niehuis, O., & Misof, B. Y. (2019) · BMC Ecology and Evolution · doi:10.1186/s12862-018-1324-9 · Cited by 230
Wood, J. G., Jones, B. C., Jiang, N., Chang, C., Hosier, S., Wickremesinghe, P., Garcia, M., Hartnett, D. A., Burhenn, L., Neretti, N., et al. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1604621113 · Cited by 214
Retrotransposon activation contributes to neurodegeneration in a Drosophila TDP-43 model of ALS
Krug, L., Chatterjee, N., Borges-Monroy, R., Hearn, S., Liao, W.-W., Morrill, K., Prazak, L., Rozhkov, N., Theodorou, D., Hammell, M., et al. (2017) · PLOS Genetics · doi:10.1371/journal.pgen.1006635 · Cited by 201
Self-citationHe, J., Babarinde, I. A., Sun, L., Xu, S., Chen, R., Shi, J., Wei, Y., Li, Y., Ma, G., Zhuang, Q., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-21808-x · Cited by 205
SQuIRE reveals locus-specific regulation of interspersed repeat expression
Yang, W. R., Ardeljan, D., Pacyna, C. N., Payer, L. M., & Burns, K. H. (2019) · Nucleic Acids Research · doi:10.1093/nar/gky1301 · Cited by 204
Gene expression hallmarks of cellular ageing
Frenk, S., & Houseley, J. (2018) · Biogerontology · doi:10.1007/s10522-018-9750-z · Cited by 181
The Metabolic Impact on Histone Acetylation and Transcription in Ageing
Peleg, S., Feller, C., Ladurner, A. G., & Imhof, A. (2016) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2016.05.008 · Cited by 178
L1 Retrotransposons and Somatic Mosaicism in the Brain
Richardson, S. R., Morell, S., & Faulkner, G. J. (2014) · Annual Review of Genetics · doi:10.1146/annurev-genet-120213-092412 · Cited by 185
The Role of Transposable Elements in Health and Diseases of the Central Nervous System
Reilly, M. T., Faulkner, G. J., Dubnau, J., Ponomarev, I., & Gage, F. H. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.3369-13.2013 · Cited by 175
Self-citationPopulation Genomics of Transposable Elements in Drosophila
Barrón, M. G., Fiston-Lavier, A.-S., Petrov, D. A., & González, J. (2014) · Annual Review of Genetics · doi:10.1146/annurev-genet-120213-092359 · Cited by 168
TRIM28 Represses Transcription of Endogenous Retroviruses in Neural Progenitor Cells
Fasching, L., Kapopoulou, A., Sachdeva, R., Petri, R., Jönsson, M. E., Männe, C., Turelli, P., Jern, P., Cammas, F. M., Trono, D., et al. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.12.004 · Cited by 150
Stress and the dynamic genome: Steroids, epigenetics, and the transposome
Hunter, R. G., Gagnidze, K., McEwen, B. S., & Pfaff, D. W. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1411260111 · Cited by 137
Widespread sex dimorphism in aging and age-related diseases
Sampathkumar, N. K., Bravo, J. I., Chen, Y., Danthi, P. S., Donahue, E. K., Lai, R. W., Lu, R. J., Randall, L. T., Vinson, N. M., & Benayoun, B. A. (2019) · Human Genetics · doi:10.1007/s00439-019-02082-w · Cited by 130
A somatic piRNA pathway in the Drosophila fat body ensures metabolic homeostasis and normal lifespan
Jones, B. C., Wood, J. G., Chang, C., Tam, A. D., Franklin, M. J., Siegel, E. R., & Helfand, S. L. (2016) · Nature Communications · doi:10.1038/ncomms13856 · Cited by 130
Chromatin structure and transposable elements in organismal aging
Wood, J. G., & Helfand, S. L. (2013) · Frontiers in Genetics · doi:10.3389/fgene.2013.00274 · Cited by 131
Gamdzyk, M., Doycheva, D. M., Araujo, C., Ocak, U., Luo, Y., Tang, J., & Zhang, J. H. (2020) · Molecular Neurobiology · doi:10.1007/s12035-020-01904-7 · Cited by 127
Genetic architecture of Alzheimer's disease
Neuner, S. M., TCW, J., & Goate, A. M. (2020) · Neurobiology of Disease · doi:10.1016/j.nbd.2020.104976 · Cited by 126
“However, with aging, the efficacy of these systems is known to be reduced, providing a genomic environment in which TEs may become activated and contribute to somatic mutagenesis (Maxwell et al., 2011; Li et al., 2013).”
BackgroundRepetitive element transcripts are elevated in the brain of C9orf72 ALS/FTLD patients
Prudencio, M., Gonzales, P. K., Cook, C. N., Gendron, T. F., Daughrity, L. M., Song, Y., Ebbert, M. T. W., van Blitterswijk, M., Zhang, Y.-J., Jansen-West, K., et al. (2017) · Human Molecular Genetics · doi:10.1093/hmg/ddx233 · Cited by 122
Transposable Elements: A Common Feature of Neurodevelopmental and Neurodegenerative Disorders
Jönsson, M. E., Garza, R., Johansson, P. A., & Jakobsson, J. (2020) · Trends in Genetics · doi:10.1016/j.tig.2020.05.004 · Cited by 122
Kuintzle, R., Chow, E. S., Westby, T. N., Gvakharia, B. O., Giebultowicz, J. M., & Hendrix, D. A. (2017) · Nature Communications · doi:10.1038/ncomms14529 · Cited by 119
Are there roles for brain cell senescence in aging and neurodegenerative disorders?
Tan, F. C. C., Hutchison, E. R., Eitan, E., & Mattson, M. P. (2014) · Biogerontology · doi:10.1007/s10522-014-9532-1 · Cited by 116
Chronic social isolation signals starvation and reduces sleep in Drosophila
Li, W., Wang, Z., Syed, S., Lyu, C., Lincoln, S., O'Neil, J. L., Nguyen, A. D., Feng, I., & Young, M. W. (2021) · Nature · doi:10.1038/s41586-021-03837-0 · Cited by 117
Self-citationUnique transposon landscapes are pervasive acrossDrosophila melanogastergenomes
Rahman, R., Chirn, G., Kanodia, A., Sytnikova, Y. A., Brembs, B., Bergman, C., & Lau, N. C. (2015) · Nucleic Acids Research · doi:10.1093/nar/gkv1193 · Cited by 111
L1 Mosaicism in Mammals: Extent, Effects, and Evolution
Faulkner, G. J., & Garcia-Perez, J. L. (2017) · Trends in Genetics · doi:10.1016/j.tig.2017.07.004 · Cited by 118
Chen, H., Zheng, X., Xiao, D., & Zheng, Y. (2016) · Aging Cell · doi:10.1111/acel.12465 · Cited by 107
The Emerging Field of Epitranscriptomics in Neurodevelopmental and Neuronal Disorders
Angelova, M. T., Dimitrova, D. G., Dinges, N., Lenče, T., Worpenberg, L., Carré, C., & Roignant, J. (2018) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2018.00046 · Cited by 109
Aging in the Brain: New Roles of Epigenetics in Cognitive Decline
Barter, J., & Foster, T. C. (2018) · The Neuroscientist · doi:10.1177/1073858418780971 · Cited by 105
Brusslan, J. A., Bonora, G., Alvarez-Canterbury, A. M. R., Tariq, F., Jaroszewicz, A., & Pellegrini, M. A. (2015) · PLANT PHYSIOLOGY · doi:10.1104/pp.114.252999 · Cited by 101
Roles for small noncoding RNAs in silencing of retrotransposons in the mammalian brain
Nandi, S., Chandramohan, D., Fioriti, L., Melnick, A. M., Hébert, J. M., Mason, C. E., Rajasethupathy, P., & Kandel, E. R. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1609287113 · Cited by 96
Engrailed homeoprotein blocks degeneration in adult dopaminergic neurons through LINE‐1 repression
de Thé, F.-X. B., Rekaik, H., Pezé-Heidsieck, E., Massiani-Beaudoin, O., Joshi, R. L., Fuchs, J., & Prochiantz, A. (2018) · The EMBO Journal · doi:10.15252/embj.201797374 · Cited by 104
The Future of Regulatory T Cell Therapy: Promises and Challenges of Implementing CAR Technology
Mohseni, Y. R., Tung, S. L., Dudreuilh, C., Lechler, R. I., Fruhwirth, G. O., & Lombardi, G. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.01608 · Cited by 95
Hazen, J. L., Faust, G. G., Rodriguez, A. R., Ferguson, W. C., Shumilina, S., Clark, R. A., Boland, M. J., Martin, G., Chubukov, P., Tsunemoto, R. K., et al. (2016) · Neuron · doi:10.1016/j.neuron.2016.02.004 · Cited by 95
Epigenetic Mechanisms Impacting Aging: A Focus on Histone Levels and Telomeres
Song, S., & Johnson, F. B. (2018) · Genes · doi:10.3390/genes9040201 · Cited by 95
Piwi Is Required to Limit Exhaustion of Aging Somatic Stem Cells
Sousa‐Victor, P., Ayyaz, A., Hayashi, R., Qi, Y., Madden, D. T., Lunyak, V. V., & Jasper, H. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.08.059 · Cited by 92
Role of Transposable Elements in Genome Stability: Implications for Health and Disease
Bhat, A., Ghatage, T., Bhan, S., Lahane, G. P., Dhar, A., Kumar, R., PANDITA, R. K., Bhat, K. M., Ramos, K. S., & Pandita, T. K. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23147802 · Cited by 82
Dysregulation of RNA Splicing in Tauopathies
Apicco, D. J., Zhang, C., Maziuk, B. F., Jiang, L., Ballance, H. I., Boudeau, S., Ung, C. Y., Li, H., & Wolozin, B. L. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.11.093 · Cited by 83
Ancient Endo-siRNA Pathways Reveal New Tricks
Claycomb, J. M. (2014) · Current Biology · doi:10.1016/j.cub.2014.06.009 · Cited by 92
Resolving the prevalence of somatic transposition in Drosophila
Treiber, C. D., & Waddell, S. (2017) · eLife · doi:10.7554/elife.28297 · Cited by 80
Activation of endogenous retroviruses during brain development causes an inflammatory response
Jönsson, M. E., Garza, R., Sharma, Y., Petri, R., Södersten, E., Johansson, J. G., Johansson, P. A., Atacho, D. A., Pircs, K., Madsen, S., et al. (2021) · The EMBO Journal · doi:10.15252/embj.2020106423 · Cited by 80
L1 retrotransposition in the soma: a field jumping ahead
Faulkner, G. J., & Billon, V. (2018) · Mobile DNA · doi:10.1186/s13100-018-0128-1 · Cited by 85
Ramirez, P., Zuniga, G., Sun, W., Beckmann, A., Ochoa, E., DeVos, S. L., Hyman, B., Chiu, G., Roy, E. R., Cao, W., et al. (2022) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2021.102181 · Cited by 79
The Y chromosome may contribute to sex-specific ageing in Drosophila
Brown, E. J., Nguyen, A. H., & Bachtrog, D. (2020) · Nature Ecology & Evolution · doi:10.1038/s41559-020-1179-5 · Cited by 84
Retrotransposon-induced mosaicism in the neural genome
Bodea, G. O., McKelvey, E. G. Z., & Faulkner, G. J. (2018) · Open Biology · doi:10.1098/rsob.180074 · Cited by 80
Epigenetic mechanisms related to cognitive decline during aging
Harman, M. F., & Martín, M. G. (2019) · Journal of Neuroscience Research · doi:10.1002/jnr.24436 · Cited by 83
The Epigenetic Control of the Transposable Element Life Cycle in Plant Genomes and Beyond
Liu, P., Cuerda-Gil, D., Shahid, S., & Slotkin, R. K. (2022) · Annual Review of Genetics · doi:10.1146/annurev-genet-072920-015534 · Cited by 69
LINE‐1 retrotransposons in healthy and diseased human brain
Suarez, N. A., Macia, Á., & Muotri, A. R. (2017) · Developmental Neurobiology · doi:10.1002/dneu.22567 · Cited by 80
Direct interrogation of the role of H3K9 in metazoan heterochromatin function
Penke, T. J. R., McKay, D. J., Strahl, B. D., Matera, A. G., & Duronio, R. J. (2016) · Genes & Development · doi:10.1101/gad.286278.116 · Cited by 74
Functional conservation in genes and pathways linking ageing and immunity
Fabian, D. K., Fuentealba, M., Dönertaş, H. M., Partridge, L., & Thornton, J. M. (2021) · Immunity & Ageing · doi:10.1186/s12979-021-00232-1 · Cited by 75
Pathogenic tau–induced transposable element–derived dsRNA drives neuroinflammation
Ochoa, E., Ramirez, P., Gonzalez, E., De Mange, J., Ray, W. J., Bieniek, K. F., & Frost, B. (2023) · Science Advances · doi:10.1126/sciadv.abq5423 · Cited by 73
Terry, D. M., & Devine, S. E. (2020) · Frontiers in Genetics · doi:10.3389/fgene.2019.01244 · Cited by 76
Repetitive elements in aging and neurodegeneration
Copley, K. E., & Shorter, J. (2023) · Trends in Genetics · doi:10.1016/j.tig.2023.02.008 · Cited by 70
The evolutionary arms race between transposable elements and piRNAs in Drosophila melanogaster
Luo, S., Zhang, H., Duan, Y., Yao, X., Clark, A. G., & Lü, J. (2020) · BMC Evolutionary Biology · doi:10.1186/s12862-020-1580-3 · Cited by 74
Chang, Y.-H., & Dubnau, J. (2019) · Current Biology · doi:10.1016/j.cub.2019.07.071 · Cited by 68
Self-citationAbe, M., Naqvi, A., Hendriks, G.-J., Feltzin, V., Zhu, Y., Grigoriev, A., & Bonini, N. M. (2014) · Genes & Development · doi:10.1101/gad.226654.113 · Cited by 68
Transposable elements as new players in neurodegenerative diseases
Ravel‐Godreuil, C., Znaidi, R., Bonnifet, T., Joshi, R. L., & Fuchs, J. (2021) · FEBS Letters · doi:10.1002/1873-3468.14205 · Cited by 77
Endogenous retroviruses in development and health
Wang, J., Lu, X., Zhang, W., & Liu, G. (2023) · Trends in Microbiology · doi:10.1016/j.tim.2023.09.006 · Cited by 72
The mechanism of ageing: primary role of transposable elements in genome disintegration
Sturm, Á., Ivics, Z., & Vellai, T. (2015) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-015-1896-0 · Cited by 75
Impact of transposable elements on insect genomes and biology
Maumus, F., Fiston-Lavier, A.-S., & Quesneville, H. (2015) · Current Opinion in Insect Science · doi:10.1016/j.cois.2015.01.001 · Cited by 63
The exonuclease Nibbler regulates age‐associated traits and modulates pi RNA length in D rosophila
Feltzin, V., Khaladkar, M., Abe, M., Parisi, M. J., Hendriks, G., Kim, J., & Bonini, N. M. (2015) · Aging Cell · doi:10.1111/acel.12323 · Cited by 62
Illuminating spatial A-to-I RNA editing signatures within the Drosophila brain
Sapiro, A. L., Shmueli, A., Henry, G. L., Li, Q., Shalit, T., Yaron, O., Paas, Y., Li, J. B., & Shohat-Ophir, G. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1811768116 · Cited by 63
Cell Cycle Re-entry in the Nervous System: From Polyploidy to Neurodegeneration
Nandakumar, S., Rozich, E., & Buttitta, L. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.698661 · Cited by 64
Gorbunova, V. A., Boeke, J. D., Helfand, S. L., & Sedivy, J. M. (2014) · Science · doi:10.1126/science.aaa3177 · Cited by 63
Death by transposition – the enemy within?
Sedivy, J. M., Kreiling, J. A., Neretti, N., Cecco, M. D., Criscione, S. W., Hofmann, J. W., Zhao, X., Ito, T., & Peterson, A. L. (2013) · BioEssays · doi:10.1002/bies.201300097 · Cited by 62
Dynamic expression of long noncoding RNAs and repeat elements in synaptic plasticity
Mååg, J. L. V., Panja, D., Sporild, I., Patil, S. S., Kaczorowski, D. C., Bramham, C. R., Dinger, M. E., & Wibrand, K. (2015) · Frontiers in Neuroscience · doi:10.3389/fnins.2015.00351 · Cited by 59
Scopa, C., Barnada, S. M., Cicardi, M. E., Singer, M., Trotti, D., & Trizzino, M. (2023) · Nature Communications · doi:10.1038/s41467-023-43728-8 · Cited by 64
Böhne, A., Sengstag, T., & Salzburger, W. (2014) · Genome Biology and Evolution · doi:10.1093/gbe/evu200 · Cited by 59
Andrenacci, D., Cavaliere, V., & Lattanzi, G. (2019) · Ageing Research Reviews · doi:10.1016/j.arr.2019.100995 · Cited by 64
Analysis of RNA-Seq Data Using TEtranscripts
Jin, Y., & Hammell, M. (2018) · Methods in molecular biology · doi:10.1007/978-1-4939-7710-9_11 · Cited by 57
Unraveling the features of somatic transposition in the Drosophila intestine
Siudeja, K., van den Beek, M., Riddiford, N., Boumard, B., Wurmser, A., Stefanutti, M., Lameiras, S., & Bardin, A. J. (2021) · The EMBO Journal · doi:10.15252/embj.2020106388 · Cited by 54
RNA editing regulates transposon-mediated heterochromatic gene silencing
Savva, Y. A., Jepson, J. E. C., Chang, Y.-J., Whitaker, R., Jones, B. C., Laurent, G. S., Tackett, M., Kapranov, P., Jiang, N., Du, G., et al. (2013) · Nature Communications · doi:10.1038/ncomms3745 · Cited by 51
The aging proteostasis decline: From nematode to human
Meller, A., & Shalgi, R. (2021) · Experimental Cell Research · doi:10.1016/j.yexcr.2021.112474 · Cited by 51
Yan, Z., Zhou, Z., Wu, Q., Chen, Z. B., Koo, E. H., & Zhong, S. (2020) · Current Biology · doi:10.1016/j.cub.2020.02.084 · Cited by 55
Endogenous retroviruses are associated with hippocampus-based memory impairment
Sankowski, R., Strohl, J. J., Huerta, T. S., Nasiri, E., Mazzarello, A. N., d’Abramo, C., Cheng, K. F., Staszewski, O., Prinz, M., Huerta, P. T., et al. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1822164116 · Cited by 49
tRNA 2′-O-methylation by a duo of TRM7/FTSJ1 proteins modulates small RNA silencing in Drosophila
Angelova, M. T., Dimitrova, D. G., Silva, B. D., Marchand, V., Jacquier, C., Achour, C., Brazane, M., Goyenvalle, C., Bourguignon‐Igel, V., Shehzada, S., et al. (2020) · Nucleic Acids Research · doi:10.1093/nar/gkaa002 · Cited by 58
Chang, Y.-H., & Dubnau, J. (2023) · Nature Communications · doi:10.1038/s41467-023-36649-z · Cited by 49
Self-citationSilencing of Transposable Elements by piRNAs in Drosophila : An Evolutionary Perspective
Luo, S., & Lü, J. (2017) · Genomics Proteomics & Bioinformatics · doi:10.1016/j.gpb.2017.01.006 · Cited by 51
The Role of Transposable Elements of the Human Genome in Neuronal Function and Pathology
Chesnokova, E., Beletskiy, A., & Kolosov, P. M. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23105847 · Cited by 51
The Piwi‐pi RNA pathway: road to immortality
Sturm, Á., Perczel, A., Ivics, Z., & Vellai, T. (2017) · Aging Cell · doi:10.1111/acel.12630 · Cited by 49
Retrotransposons in the development and progression of amyotrophic lateral sclerosis
Savage, A. L., Schumann, G. G., Breen, G. D., Bubb, V. J., Al‐Chalabi, A., & Quinn, J. P. (2018) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp-2018-319210 · Cited by 53
Romano, G., Klima, R., & Feiguin, F. (2020) · BMC Biology · doi:10.1186/s12915-020-00816-1 · Cited by 47
Viruses and Endogenous Retroviruses as Roots for Neuroinflammation and Neurodegenerative Diseases
Römer, C. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.648629 · Cited by 48
Nguyen, A. H., & Bachtrog, D. (2021) · PLoS Genetics · doi:10.1371/journal.pgen.1009438 · Cited by 47
The Physiology of Homeoprotein Transduction
Nardo, A. A. D., Fuchs, J., Joshi, R. L., Moya, K. L., & Prochiantz, A. (2018) · Physiological Reviews · doi:10.1152/physrev.00018.2017 · Cited by 52
Metadata
- Authors
- Li, W., Prazak, L., Chatterjee, N., Grüninger, S., Krug, L., Theodorou, D., & Dubnau, J.
- Affiliations
- Cold Spring Harbor Laboratory (US)
- University of Zurich (CH)
- Sorbonne Paris Cité (FR)
- Corresponding author
- Dubnau, Josh
- ORCID
- Venue
- Nature Neuroscience
- Published
- 2013-04-07
- Volume
- 16
- Issue
- 5
- Pages
- 529-531
- ISSN
- 1097-6256 (ISSN-L)
- 1546-1726
- PMC
- PMC3821974
- OpenAlex
- W2089023364
- Cited by
- 346
- References
- 24
- Citations by year
- 2026: 15 · 2025: 25 · 2024: 30 · 2023: 22 · 2022: 32 · 2021: 39 · 2020: 38 · 2019: 27 · 2018: 23 · 2017: 22 · 2016: 22 · 2015: 25 · 2014: 20 · 2013: 6
- FWCI
- 8.63
- Type
- journal article
- Language
- en
- Open access
- green
- www.zora.uzh.ch
- Licence
- other-oa
- www.springer.com/tdm (tdm)
- Locations
- Nature Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- Zurich Open Repository and Archive (University of Zurich) (acceptedVersion, other-oa)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Cold Spring Harbor Laboratory Institutional Repository (Cold Spring Harbor Laboratory) (acceptedVersion)
- Zurich Open Repository and Archive (University of Zurich) (submittedVersion, other-oa)
- Zurich Open Repository and Archive (University of Zurich)
- Funders
- National Institute of Neurological Disorders and Stroke (TR01 5R01NS067690-03, R01NS067690)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Chromosomal and Genetic Variations
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurobiology and Insect Physiology Research
- Keywords
- transposable elements, transposon activation, aging, Argonaute 2, RNA interference, memory impairment, lifespan, Drosophila brain, age-related neurodegeneration
- MeSH terms
- Aging, Analysis of Variance, Animals, Avoidance Learning, Brain, Conditioning, Classical, DNA Transposable Elements, Drosophila, Longevity, Mutation, Neurons, Drosophila Proteins, Animals, Genetically Modified, Green Fluorescent Proteins, Argonaute Proteins
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