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.
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“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
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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
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Dragomir, M. P., Knutsen, E., & Călin, G. A. (2021) · Trends in Genetics · doi:10.1016/j.tig.2021.10.002 · Cited by 198
MirGeneDB 2.1: toward a complete sampling of all major animal phyla
Fromm, B., Høye, E., Domanska, D., Zhong, X., Aparicio-Puerta, E., Ovchinnikov, V., Umu, S. U., Chabot, P. J., Kang, W., Aslanzadeh, M., et al. (2022) · Nucleic Acids Research · doi:10.1093/nar/gkab1101 · Cited by 147
miRNAs; a novel strategy for the treatment of COVID‐19
Ying, H., Ebrahimi, M., Keivan, M., Khoshnam, S. E., Salahi, S., & Farzaneh, M. (2021) · Cell Biology International · doi:10.1002/cbin.11653 · Cited by 86
Motif-Aware miRNA-Disease Association Prediction via Hierarchical Attention Network
Zhao, B.-W., He, Y.-Z., Su, X., Yang, Y., Li, G., Huang, Y., Hu, P., You, Z., & Hu, L. (2024) · IEEE Journal of Biomedical and Health Informatics · doi:10.1109/jbhi.2024.3383591 · Cited by 61
A plant immune protein enables broad antitumor response by rescuing microRNA deficiency
Qi, Y., Ding, L., Zhang, S., Yao, S., Ong, J., Li, Y., Wu, H., & Du, P. (2022) · Cell · doi:10.1016/j.cell.2022.04.030 · Cited by 58
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
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