The DOI matches its Crossref record; 128 of the 130 references it cites were found in a registry or an index.
The roles of microRNAs in mouse development
Abstract
Hundreds of microRNAs (miRNAs) are expressed in distinct spatial and temporal patterns during embryonic and postnatal mouse development. The loss of all miRNAs through the deletion of critical miRNA biogenesis factors results in early lethality. The function of each miRNA stems from their cumulative negative regulation of multiple mRNA targets expressed in a particular cell type. During development, miRNAs often coordinate the timing and direction of cell fate transitions. In adults, miRNAs frequently contribute to organismal fitness through homeostatic roles in physiology. Here, we review how the recent dissection of miRNA-knockout phenotypes in mice as well as advances related to their targets, dosage, and interactions have collectively informed our understanding of the roles of miRNAs in mammalian development and adaptive responses.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
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?
In the citing paper
“Many miRNAs also display tissue-, cell type-, or conditionspecific expression patterns and play key roles in the regulation of developmental programs (DeVeale et al., 2021;Manakov et al., 2009).”
From Scalable and deep profiling of mRNA targets for individual microRNAs with chimeric eCLIP (2022) · cites this paper as DeVeale et al., 2021
Citations
Cites
Bartel (2004) · doi:10.1016/s0092-8674(04)00045-5 · Cited by 34,714
The C. elegans heterochronic gene lin-4 encodes small RNAs with antisense complementarity to lin-14
Lee, R. C., Feinbaum, R. L., & Ambros, V. (1993) · Cell · doi:10.1016/0092-8674(93)90529-y · Cited by 12,948
Most mammalian mRNAs are conserved targets of microRNAs
Friedman, R. C., Farh, K. K.-H., Burge, C. B., & Bartel, D. P. (2009) · Genome Research · doi:10.1101/gr.082701.108 · Cited by 8,462
Natural RNA circles function as efficient microRNA sponges
Hansen, T. B., Jensen, T. I., Clausen, B. H., Bramsen, J. B., Finsen, B., Damgaard, C. K., & Kjems, J. (2013) · Nature · doi:10.1038/nature11993 · Cited by 7,985
Predicting effective microRNA target sites in mammalian mRNAs
Agarwal, V., Bell, G. W., Nam, J.-W., & Bartel, D. P. (2015) · eLife · doi:10.7554/elife.05005 · Cited by 7,318
The 21-nucleotide let-7 RNA regulates developmental timing in Caenorhabditis elegans
Reinhart, B. J., Slack, F. J., Basson, M., Pasquinelli, A. E., Bettinger, J. C., Rougvie, A. E., Horvitz, H. R., & Ruvkun, G. (2000) · Nature · doi:10.1038/35002607 · Cited by 4,989
Korn, T., Bettelli, E., Oukka, M., & Kuchroo, V. K. (2009) · Annual Review of Immunology · doi:10.1146/annurev.immunol.021908.132710 · Cited by 4,873
The widespread regulation of microRNA biogenesis, function and decay
Krol, J., Loedige, I., & Filipowicz, W. (2010) · Nature Reviews Genetics · doi:10.1038/nrg2843 · Cited by 4,672
MicroRNA Targeting Specificity in Mammals: Determinants beyond Seed Pairing
Grimson, A., Farh, K. K.-H., Johnston, W. K., Garrett-Engele, P., Lim, L. P., & Bartel, D. P. (2007) · Molecular Cell · doi:10.1016/j.molcel.2007.06.017 · Cited by 3,766
Bartel, D. P. (2018) · Cell · doi:10.1016/j.cell.2018.03.006 · Cited by 3,751
Cited by
Sorted by citations
Items 101–122 of 122
Wu, Q., Zhang, Y., Bai, F., Wu, Y., Hu, Y., & Wu, J. (2025) · Cell & Bioscience · doi:10.1186/s13578-025-01468-w · Cited by 1
Hu, Z., Guo, L., Xu, H., Yang, T., Chen, J., Yang, S., Liu, Y., & Wang, Y. N. (2026) · Poultry Science · doi:10.1016/j.psj.2026.107197 · Cited by 1
He, F. F., Li, M., Chen, F., Zhou, R., Qi, M., Fu, B., Zhang, H., Li, Q., Bi, Y., & Huang, T. (2024) · Animals · doi:10.3390/ani15010046 · Cited by 1
Campos‐Melo, D., Droppelmann, C. A., & Zhu, L. Q. (2023) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2023.1166943 · Cited by 1
Morphological profiling of all human and mouse miRNAs in 24M cellsPreprint
Wagner, J., Smillie, C. L., Sirey, T., Khamseh, A., Ponting, C. P., & Beentjes, S. V. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.11.14.687149 · Cited by 1
González‐Martínez, J., Sánchez-Belmonte, A., Ayala, E., García, A., Nogueira, E., Muñoz, J., Melati, A., Giménez-Llorente, D., Losada, A., Ortega, S., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.02.06.579214
Романюк, С. И., & Комісаренко, С. В. (2024) · Visnik Nacional noi academii nauk Ukrai ni · doi:10.15407/visn2024.12.003
Wang, W., Zhang, F., Lu, M., Wu, X., Yu, Z., Yang, J., Cai, X., Lin, Q., Fan, Y., Xu, J. Y., et al. (2025) · Life Science and Technology · doi:10.57237/j.life.2025.01.002
Yamakawa, S., Yamazaki, A. K., Morino, Y., & Wada, H. (2024) · Figshare · doi:10.6084/m9.figshare.26584965
In vivo AGO-APP for cell-type- and compartment-specific miRNA profiling in the mouse brain
Surbhi, S., Erni, A., Vincenzi, F., Tessier, B., Venugopal, V., Meister, G., Favereaux, A., Cremer, H., & Béclin, C. (2025) · Cell Reports Methods · doi:10.1016/j.crmeth.2025.101267
The Epigenetic Angle in the Precision Medicine Era for Blood Disorder Advancements
Hamdy, N. Μ., Abulsoud, A. I., Rizk, N. I., AL‐Noshokaty, T. M., Zaki, M. B., Sultan, A. S., & Doghish, A. S. (2026) · Sub-cellular biochemistry/Subcellular biochemistry · doi:10.1007/978-3-032-08530-6_6
The harmonies played by miR-302/367 cluster in pluripotency, reprogramming, and rejuvenation
Zamanian, M., Moradi, S., & Baharvand, H. (2026) · Stem Cells Translational Medicine · doi:10.1093/stcltm/szaf072
Non-Coding RNA: Architects of Cellular Complexity and Agents of Malignancy
Shah, A. (2026) · Genes · doi:10.3390/genes17030304
Kanlı, Z., Eyüboğlu, İ. P., Arğa, K. Y., Aydın, B., Erzık, C., & Cabadak, H. (2026) · Biochemical Genetics · doi:10.1007/s10528-026-11412-3
Cerebellar microRNA-206 Tunes Purkinje Neuron Firing Dynamics to Control Sensorimotor GatingPreprint
Heyer, M. P., Ishikawa, M., Wang, J., Evangelista, J. E., Fakira, A. K., Ma’ayan, A., Feng, G., & Kenny, P. J. (2026) · SSRN Electronic Journal · doi:10.64898/2026.06.29.734826
Functional delivery of commercially available microRNA mimics to the organs of developing mice
Willen, S., Myti, D., Obeidat, R. M., Casado, F., Khaghani-Razi-Abad, S., Nardiello, C., Günther, S., Haberkant, P., Stein, F., Khan, M. M., et al. (2026) · RNA · doi:10.1261/rna.081174.126
DGCR8 promotes nascent transcription independently of DROSHA
Wang, J., Cai, Y., Wang, D., Shen, H., & Xu, W. (2026) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2026.154379
Chu, Q., Zhou, J., Bai, Y., Zhang, L., Li, M., Su, X., & Wang, K. (2026) · Comparative Biochemistry and Physiology Part D Genomics and Proteomics · doi:10.1016/j.cbd.2026.101963
Guo, X., Gao, C., Chen, Z., Lu, S., Wang, L., Li, W., He, X., Yang, C., Li, J., & Chen, S. (2026) · Biology · doi:10.3390/biology15161379
Canonical and isomiR products of miR-142 enhance dendritic cell reprogramming
Arh, N., Курочкин, И., Vaz, B. L., Schaefer, D., Geukens, C., Rosa, F. A., & Pereira, C. (2026) · Cell Reports · doi:10.1016/j.celrep.2026.117825
Zhou, J., Wu, Y., Chai, Y., Zhang, P., & Yuan, R. (2026) · Biosensors and Bioelectronics · doi:10.1016/j.bios.2026.119150
Behdani, M., Hashemi, M., Kaykhaei, M. A., Bahari, M., Taheri, M., & Bahari, G. (2026) · BioMed Research International · doi:10.1155/bmri/8927160
Metadata
- Authors
- DeVeale, B., Swindlehurst-Chan, J., & Blelloch, R.
- Affiliations
- University of California, San Francisco (US)
- Corresponding author
- Blelloch, Robert
- Venue
- Nature Reviews Genetics
- Published
- 2021-01-15
- Volume
- 22
- Issue
- 5
- Pages
- 307-323
- ISSN
- 1471-0056 (ISSN-L)
- 1471-0064
- OpenAlex
- W3123282374
- Cited by
- 121
- References
- 130
- Citations by year
- 2026: 15 · 2025: 21 · 2024: 23 · 2023: 27 · 2022: 23 · 2021: 12
- FWCI
- 2.59
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- Locations
- Nature Reviews Genetics (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Canadian Institutes of Health Research
- National Institute of General Medical Sciences (R01GM122439, R01GM125089)
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (R21HD093084, P50HD055764)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › MicroRNA in disease regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Molecular Biology Research
- Keywords
- microRNA, mouse development, microRNA biogenesis, miRNA target genes, cell fate transitions, embryonic development, postnatal development, non-coding RNA, homeostasis, adaptive response
- MeSH terms
- Animals, Cell Differentiation, Growth, Cell Lineage, MicroRNAs, Embryonic Development, Mice
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