The DOI matches its Crossref record; 39 of the 39 references it cites were found in a registry or an index.
Fragile X-Related Proteins Regulate Mammalian Circadian Behavioral Rhythms
Open accessAbstract
Fragile X syndrome results from the absence of the fragile X mental retardation 1 (FMR1) gene product (FMRP). FMR1 has two paralogs in vertebrates: fragile X related gene 1 and 2 (FXR1 and FXR2). Here we show that Fmr1/Fxr2 double knockout (KO) and Fmr1 KO/Fxr2 heterozygous animals exhibit a loss of rhythmic activity in a light:dark (LD) cycle, and that Fmr1 or Fxr2 KO mice display a shorter free-running period of locomotor activity in total darkness (DD). Molecular analysis and in vitro electrophysiological studies suggest essentially normal function of cells in the suprachiasmatic nucleus (SCN) in Fmr1/Fxr2 double KO mice. However, the cyclical patterns of abundance of several core clock component messenger (m) RNAs are altered in the livers of double KO mice. Furthermore, FXR2P alone or FMRP and FXR2P together can increase PER1- or PER2-mediated BMAL1-Neuronal PAS2 (NPAS2) transcriptional activity in a dose-dependent manner. These data collectively demonstrate that FMR1 and FXR2 are required for the presence of rhythmic circadian behavior in mammals and suggest that this role may be relevant to sleep and other behavioral alterations observed in fragile X patients.
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
“This effect could be due to the fact that the absence of FMRP is likely compensated by FXR1P and/or FXR2P, as reported for other phenotypes (Zhang et al., 2008).”
From New insights into the regulatory function of CYFIP1 in the context of WAVE- and FMRP-containing complexes (2017) · cites this paper as Zhang et al., 2008
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease
Chirgwin, J. M., Przybyla, A., MacDonald, R. J., & Rutter, W. J. (1979) · Biochemistry · doi:10.1021/bi00591a005 · Cited by 21,460
Coordination of circadian timing in mammals
Reppert, S. M., & Weaver, D. R. (2002) · Nature · doi:10.1038/nature00965 · Cited by 4,379
Verkerk, A. J. M. H., Pieretti, M., Sutcliffe, J. S., Fu, Y.-H., Kuhl, D. P. A., Pizzuti, A., Reiner, O., Richards, S., Victoria, M. F., Zhang, F., et al. (1991) · Cell · doi:10.1016/0092-8674(91)90397-h · Cited by 3,481
Self-citationCoordinated memory replay in the visual cortex and hippocampus during sleep
Ji, D., & Wilson, M. A. (2007) · Nature Neuroscience · doi:10.1038/nn1825 · Cited by 1,669
The mGluR theory of fragile X mental retardation
Bear, M. F., Huber, K. M., & Warren, S. T. (2004) · Trends in Neurosciences · doi:10.1016/j.tins.2004.04.009 · Cited by 1,580
Fmr1 knockout mice: A model to study fragile X mental retardation
THEDUTCHBELGIANFRAGILEXCONSOR (1994) · Cell · doi:10.1016/0092-8674(94)90569-x · Cited by 1,108
Mammalian circadian biology: elucidating genome-wide levels of temporal organization
Lowrey, P. L., & Takahashi, J. S. (2004) · Annual Review of Genomics and Human Genetics · doi:10.1146/annurev.genom.5.061903.175925 · Cited by 976
Post-translational modifications regulate the ticking of the circadian clock
Gallego, M., & Virshup, D. M. (2007) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2106 · Cited by 881
A Differential Response of Two Putative Mammalian Circadian Regulators, mper1and mper2, to Light
Albrecht, U., Sun, Z. S., Eichele, G., & Lee, C. C. (1997) · Cell · doi:10.1016/s0092-8674(00)80495-x · Cited by 879
Self-citationDevys, D., Lutz, Y., Rouyer, N., Bellocq, J., & Mandel, J. (1993) · Nature Genetics · doi:10.1038/ng0893-335 · Cited by 781
Flagged first, then by citations
Cited by
Sorted by citations
Items 101–131 of 131
Effect of Epigenetic Differences in Identical Twins
Schwab, T. L., & Hogenson, T. L. (2019) · Handbook of Nutrition, Diet, and Epigenetics · doi:10.1007/978-3-319-55530-0_65 · Cited by 3
Wang, H. B., Smale, N. E., Brown, S. H., Villanueva, S. A. M. B., Zhou, D., Mulji, A., Bhandal, D. S., Nguyen-Ngo, K., Harvey, J. R., Ghiani, C. A., et al. (2025) · eLife · doi:10.7554/elife.104720 · Cited by 3
FMRP binds Per1 mRNA and downregulates its protein expression in mice
Tang, X., Zhang, J., Li, X., Hu, Y., Liu, D., Li, J., & Lu, R. (2023) · Molecular Brain · doi:10.1186/s13041-023-01023-z · Cited by 2
Self-citationDo metabolic deficits contribute to sleep disruption in monogenic intellectual disability syndromes?
Valencia, M. L., Sofela, F. A., Jongens, T. A., & Sehgal, A. (2024) · Trends in Neurosciences · doi:10.1016/j.tins.2024.06.006 · Cited by 2
Role of microRNAs in Autism Spectrum Disorder
Sarachana, T., & Hu, V. W. (2013) · Wiley eBooks · doi:10.1002/9781118695999.ch14 · Cited by 2
Milojević, S., Ghosh, A., Makević, V., Stojković, M., Capovilla, M., Tosti, T. B., Budimirovic, D. B., & Protic, D. D. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25147949 · Cited by 1
Co-designing Nova Sleepcare: identifying priority areas for implementation
Nahal, I. K., Estes, M. L., Currie, G., Heathcote, C., Heathcote, G., Deliscar, E., Deliscar, S., Thomas, M. R., Richardson, A., Dewey, D., et al. (2026) · Frontiers in Pediatrics · doi:10.3389/fped.2026.1760214 · Cited by 1
Sleep-dependent cellular chemical changes in the aging brain
Wang, G. X., & Mourrain, P. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-800136-3.00006-5 · Cited by 1
Sleep in Children with Neurodevelopmental Disorders
Richdale, A. L., Baker, E. K., & Sciberras, E. (2022) · Springer eBooks · doi:10.1007/978-981-19-5791-8_20 · Cited by 1
Effect of Epigenetic Differences in Identical Twins
Schwab, T. L., & Hogenson, T. L. (2017) · Springer eBooks · doi:10.1007/978-3-319-31143-2_65-1 · Cited by 1
Insights into the human Fragile X syndrome gene family using Drosophila melanogaster
Coffee, R. L. (2011) · Cited by 1
Daily oscillation of the excitation/inhibition ratio is disrupted in two mouse models of autismPreprint
Bridi, M., Luo, N., Kim, G., O’Ferrall, C., Patel, R. V., Bertrand, S. J., Kannan, S., & Kirkwood, A. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.07.05.451213 · Cited by 1
Wang, H. B., Smale, N. E., Brown, S. H., Villanueva, S. A. M. B., Zhou, D., Mulji, A., Bhandal, D. S., Nguyen-Ngo, K., Harvey, J. R., Ghiani, C. A., et al. (2025) · eLife · doi:10.7554/elife.104720.1 · Cited by 1
Wang, H. B., Smale, N. E., Brown, S. H., Villanueva, S. A. M. B., Zhou, D., Mulji, A., Bhandal, D. S., Nguyen-Ngo, K., Harvey, J. R., Ghiani, C. A., et al. (2025) · eLife · doi:10.7554/elife.104720.3 · Cited by 1
Clocks, Brain Function, and Dysfunction
Feillet, C. A., & Albrecht, U. (2009) · Springer eBooks · doi:10.1007/978-1-4419-1262-6_10
Self-citationSocial dysfunction and mental retardation
Pietropaolo, S., Sluyter, F., & Crusio, W. E. (2014) · Cambridge University Press eBooks · doi:10.1017/cbo9781107360556.010
Strumbos, J. G., & Brown, M. R. (2010)
Exploring a Role for Sleep in Neural Development and Psychiatric Disease
Kayser, M. S. (2013) · Journal of Sleep Disorders & Therapy · doi:10.4172/2167-0277.1000106
Sleep in children with genetic disorders
Licis, A. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-822963-7.00224-3
Wang, H. B., Smale, N. E., Brown, S. H., Villanueva, S. A. M. B., Zhou, D., Mulji, A., Bhandal, D. S., Nguyen-Ngo, K., Harvey, J. R., Ghiani, C. A., et al. (2025) · eLife · doi:10.7554/elife.104720.2
Sleep in a mouse model of fragile X syndrome is resistant to metabolic manipulations
Valencia, M. L., Aponte, R. A. V., Baur, J. A., Jongens, T. A., & Sehgal, A. (2025) · Human Molecular Genetics · doi:10.1093/hmg/ddaf149
Current and emerging tools for studying animal models of sleep and autism
Kyriakakis, P., & Gonzalez, O. C. (2025) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2025.11.031
Additional file 1 of FMRP binds Per1 mRNA and downregulates its protein expression in mice
Tang, X., Zhang, J., Li, X., Hu, Y., Liu, D., Li, J.-D., & Lu, R. (2024) · Figshare · doi:10.6084/m9.figshare.26580590
Self-citationAdditional file 1 of Tau reduction attenuates autism-like features in Fmr1 knockout mice
Zhao, S., Jiang, X., Han, L., Jiang, Y., Wang, Y., Meng, J., Zhu, X., Zhang, X., Luo, H., & Zhang, Y.-W. (2023) · Figshare · doi:10.6084/m9.figshare.24522666
Rôle du long ARN non codant Neat1 dans la rythmicité circadienne hypophysaire
Torres, M. (2018) · theses.fr (ABES) · doi:10.70675/0be62982z380ez416dzbc04zb92ab61b6e88
Felgerolle, C. (2019) · theses.fr (ABES) · doi:10.70675/fbd5cf69zed5az4a57zbfdez48e26a937a72
Spatial control of nucleoporin condensation by Fragile X-related proteins
Agote‐Arán, A. (2020) · theses.fr (ABES) · doi:10.70675/4a7c9911z5df2z4b98zaf99z156d40ddf6f7
Bmal2, a circadian-related gene as candidate in obesity and diabetes
Philippe, M. (2023) · theses.fr (ABES) · doi:10.70675/0649c89czc015z4d7fz8832z596152e96dc1
Pathophysiology of the FMRP-R138Q Fragile X Syndrome missense mutation in mice
Chato-Astrain, I. (2025) · theses.fr (ABES) · doi:10.70675/ce8d1ccfz4554z4c55z8782z624e392f72a1
Wu, Y., Wu, D., Zhong, W., & Ma, J. (2026) · ALPHA PSYCHIATRY · doi:10.31083/ap52264
Palacios-Muñoz, A. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27188129
Metadata
- Authors
- Zhang, J., Fang, Z., Jud, C., Vansteensel, M. J., Kaasik, K., Lee, C. C., Albrecht, U., Tamanini, F., Meijer, J. H., Oostra, B. A., & Nelson, D. L.
- Affiliations
- Baylor College of Medicine (US)
- University of Fribourg (CH)
- Leiden University Medical Center (NL)
- The University of Texas Health Science Center at Houston (US)
- Erasmus MC (NL)
- Corresponding author
- Nelson, David L.
- ORCID
- Venue
- The American Journal of Human Genetics
- Publisher
- Elsevier BV
- Published
- 2008-07
- Volume
- 83
- Issue
- 1
- Pages
- 43-52
- ISSN
- 0002-9297 (ISSN-L)
- PMC
- PMC2443847
- OpenAlex
- W2107880079
- Cited by
- 131
- References
- 39
- Citations by year
- 2026: 3 · 2025: 9 · 2024: 7 · 2023: 8 · 2022: 5 · 2021: 5 · 2020: 6 · 2019: 8 · 2018: 8 · 2017: 8 · 2016: 6 · 2015: 6 · 2014: 9 · 2013: 8 · 2012: 4
- FWCI
- 4.59
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- The American Journal of Human Genetics (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- EUR Research Repository (Erasmus University Rotterdam) (publishedVersion)
- reroDoc Digital Library (submittedVersion)
- EUR Research Repository (Erasmus University Rotterdam) (submittedVersion)
- RePub (Erasmus University Rotterdam) (submittedVersion, other-oa)
- RePub (Erasmus University Rotterdam) (submittedVersion)
- Funders
- Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
- National Institutes of Health
- Intellectual and Developmental Disabilities Research Center
- National Institute of Child Health and Human Development
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (HD 24064, HD-38038, P30HD024064, R01HD038038)
- Topics
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Circadian rhythm and melatonin
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
- Life Sciences › Neuroscience › Cognitive Neuroscience › Sleep and Wakefulness Research
- Keywords
- fragile X syndrome, FMRP, FXR1, FXR2, circadian rhythm, locomotor activity, suprachiasmatic nucleus, clock genes, Per1, Per2, Bmal1, NPAS2, sleep, liver transcriptome
- MeSH terms
- Animals, Behavior, Animal, Circadian Rhythm, Electrophysiology, Flavoproteins, Fragile X Syndrome, Gene Expression Regulation, Heterozygote, Liver, Male, Mammals, Mice, Inbred C57BL, Motor Activity, Nerve Tissue Proteins, Neurons, Nuclear Proteins, RNA, Messenger, Suprachiasmatic Nucleus, Time Factors, Transcription Factors, RNA-Binding Proteins, In Situ Hybridization, Mice, Knockout, Cell Cycle Proteins, Mice, Basic Helix-Loop-Helix Transcription Factors, Basic Helix-Loop-Helix Proteins, ARNTL Transcription Factors, Cryptochromes, Period Circadian 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