The DOI matches its Crossref record; 24 of the 24 references it cites were found in a registry or an index.
The nuclear matrix protein Matr3 regulates processing of the synaptic microRNA-138-5p
Abstract
microRNA-dependent post-transcriptional control represents an important gene-regulatory layer in post-mitotic neuronal development and synaptic plasticity. We recently identified the brain-enriched miR-138 as a negative regulator of dendritic spine morphogenesis in rat hippocampal neurons. A potential involvement of miR-138 in cognition is further supported by a recent GWAS study on memory performance in a cohort of aged (>60 years) individuals. The expression of miR-138, which is encoded in two independent genomic loci (miR-138-1 and -2), is subject to both cell-type and developmental stage-specific regulation, the underlying molecular mechanisms however are poorly understood. Here, we show that miR-138-2 is the primary source of mature miR-138 in developing rat hippocampal neurons. Furthermore, we obtained evidence for the regulation of miR-138-2 biogenesis at the level of primary miRNA processing. Using biochemical pull-down assays, we identified the nuclear matrix protein Matrin-3 as pri/pre-miR-138 interacting protein and mapped the interaction to the pri/pre-miR-138-2 loop region. Matrin-3 loss-of-function experiments in HEK293 cells and primary neurons together with protein localization studies suggest an inhibitory function of Matrin-3 in nuclear pri-miR-138-2 processing. Together, our experiments unravel a new mechanism of miR-138 regulation in neurons, with important implications for miR-138 regulation during neuronal development, synaptic plasticity and memory-rela…
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“It has been described that mir-138-5p increases its expression during neuronal development in vitro [69]”
From MicroRNA-138-5p Targets Pro-Apoptotic Factors and Favors Neural Cell Survival: Analysis in the Injured Spinal Cord (2022) · cites this paper as [69]
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Dicer1 and miR-219 Are Required for Normal Oligodendrocyte Differentiation and Myelination
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Self-citationPost-transcriptional regulation of microRNA expression
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Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis
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Self-citationA Compendium of RNA-Binding Proteins that Regulate MicroRNA Biogenesis
Treiber, T., Treiber, N., Plessmann, U., Harlander, S., Daiß, J.-L., Eichner, N., Lehmann, G., Schall, K., Urlaub, H., & Meister, G. (2017) · Molecular Cell · doi:10.1016/j.molcel.2017.03.014 · Cited by 302
Self-citationAltered microRNA regulation in Huntington's disease models
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Potent degradation of neuronal miRNAs induced by highly complementary targets
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Activity-dependent spatially localized miRNA maturation in neuronal dendrites
Sambandan, S., Akbalık, G., Kochen, L., Rinne, J. S., Kahlstatt, J., Glock, C., Tushev, G., Alvarez‐Castelao, B., Heckel, A., & Schuman, E. M. (2017) · Science · doi:10.1126/science.aaf8995 · Cited by 187
Cited by
MicroRNAs as regulators of brain function and targets for treatment of epilepsy
Brennan, G. P., & Henshall, D. C. (2020) · Nature Reviews Neurology · doi:10.1038/s41582-020-0369-8 · Cited by 169
Maza, R. M., Barreda-Manso, M. A., Reigada, D., Silván, Á., Muñoz-Galdeano, T., Soto, A., del Águila, Á., & Nieto-Díaz, M. (2022) · Biomedicines · doi:10.3390/biomedicines10071559 · Cited by 12
Metadata
- Authors
- Weiss, K., Treiber, T., Meister, G., & Schratt, G.
- Venue
- Neurobiology of Learning and Memory
- Publisher
- Elsevier BV
- Published
- 2019-03
- Volume
- 159
- Pages
- 36-45
- ISSN
- 1074-7427
- Cited by
- 18
- References
- 24
- Language
- en
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- Funders
- Deutsche Forschungsgemeinschaft (SCHR 1136/8-1)
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- Weiss, K., Treiber, T., Meister, G., & Schratt, G. (2019). The nuclear matrix protein Matr3 regulates processing of the synaptic microRNA-138-5p. Neurobiology of Learning and Memory. https://doi.org/10.1016/j.nlm.2019.02.008
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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