MicroRNAs as Neuronal Fate Determinants.
(2014) In Neuroscientist 20(3). p.235-242- Abstract
- Since the discovery of short, regulatory microRNAs (miRNA) 20 years ago, the understanding of their impact on gene regulation has dramatically increased. Differentiation of cells requires comprehensive changes in regulatory networks at all levels of gene expression. Posttranscriptional regulation by miRNA leads to rapid modifications in the protein level of large gene networks, and it is therefore not surprising that miRNAs have been found to influence the fate of differentiating cells. Several recent studies have shown that overexpression of a single miRNA in different cellular contexts results in forced differentiation of nerve cells. Loss of this miRNA constrains neurogenesis and promotes gliogenesis. This miRNA, miR-124, is probably... (More)
- Since the discovery of short, regulatory microRNAs (miRNA) 20 years ago, the understanding of their impact on gene regulation has dramatically increased. Differentiation of cells requires comprehensive changes in regulatory networks at all levels of gene expression. Posttranscriptional regulation by miRNA leads to rapid modifications in the protein level of large gene networks, and it is therefore not surprising that miRNAs have been found to influence the fate of differentiating cells. Several recent studies have shown that overexpression of a single miRNA in different cellular contexts results in forced differentiation of nerve cells. Loss of this miRNA constrains neurogenesis and promotes gliogenesis. This miRNA, miR-124, is probably the most well-documented example of a miRNA that controls nerve cell fate determination. In this review we summarize the recent findings on miR-124, potential molecular mechanisms used by miR-124 to drive neuronal differentiation, and outline future directions. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/3955674
- author
- Åkerblom, Malin LU and Jakobsson, Johan LU
- organization
- publishing date
- 2014
- type
- Contribution to journal
- publication status
- published
- subject
- in
- Neuroscientist
- volume
- 20
- issue
- 3
- pages
- 235 - 242
- publisher
- SAGE Publications
- external identifiers
-
- pmid:23877999
- wos:000336265200009
- scopus:84900852879
- pmid:23877999
- ISSN
- 1089-4098
- DOI
- 10.1177/1073858413497265
- language
- English
- LU publication?
- yes
- id
- ae99faf6-6920-432a-820e-123aefe55c44 (old id 3955674)
- alternative location
- http://www.ncbi.nlm.nih.gov/pubmed/23877999?dopt=Abstract
- date added to LUP
- 2016-04-01 10:06:55
- date last changed
- 2022-02-09 22:51:03
@article{ae99faf6-6920-432a-820e-123aefe55c44, abstract = {{Since the discovery of short, regulatory microRNAs (miRNA) 20 years ago, the understanding of their impact on gene regulation has dramatically increased. Differentiation of cells requires comprehensive changes in regulatory networks at all levels of gene expression. Posttranscriptional regulation by miRNA leads to rapid modifications in the protein level of large gene networks, and it is therefore not surprising that miRNAs have been found to influence the fate of differentiating cells. Several recent studies have shown that overexpression of a single miRNA in different cellular contexts results in forced differentiation of nerve cells. Loss of this miRNA constrains neurogenesis and promotes gliogenesis. This miRNA, miR-124, is probably the most well-documented example of a miRNA that controls nerve cell fate determination. In this review we summarize the recent findings on miR-124, potential molecular mechanisms used by miR-124 to drive neuronal differentiation, and outline future directions.}}, author = {{Åkerblom, Malin and Jakobsson, Johan}}, issn = {{1089-4098}}, language = {{eng}}, number = {{3}}, pages = {{235--242}}, publisher = {{SAGE Publications}}, series = {{Neuroscientist}}, title = {{MicroRNAs as Neuronal Fate Determinants.}}, url = {{http://dx.doi.org/10.1177/1073858413497265}}, doi = {{10.1177/1073858413497265}}, volume = {{20}}, year = {{2014}}, }