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MiR-302/367 regulate neural progenitor proliferation, differentiation timing, and survival in neurulation

Yang, Si-Lu, Yang, Mei, Herrlinger, Stephanie, Liang, Chen, Lai, Fan, Chen, Jian-Fu·2015·Developmental Biology
DOI 10.1016/j.ydbio.2015.09.020PMC PMC4688151
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  • miR-302 regulates neural progenitor proliferation, differentiation timing, and survival during neurulation; knockout results in early embryonic lethality and open neural tube defects.

    “For example, miR-302, which we have found to be highly enriched in exosomes, has been shown to regulate neural progenitor proliferation, differentiation timing, and survival during neurulation, and knockout or miR-302 results in early embryonic lethality and open neural tube defects [28].”

    From Distinct repertoires of microRNAs present in mouse astrocytes compared to astrocyte-secreted exosomes (2017) · cites this paper as [28]

    The Abstract reports that deletion of the miR-302/367 cluster caused early embryonic lethality and open neural tube defects, with altered neural progenitor proliferation, differentiation, and survival. The Discussion clarifies that this study deleted both miR-302 and miR-367, so its knockout and cell-survival findings cannot be attributed to miR-302 alone. (LLM, conf=0.88)

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Cited by

Sorted by citations

Authors
Yang, S.-L., Yang, M., Herrlinger, S., Liang, C., Lai, F., & Chen, J.-F.
Venue
Developmental Biology
Publisher
Elsevier BV
Published
2015-12
Volume
408
Issue
1
Pages
140-150
ISSN
0012-1606
DOI
10.1016/j.ydbio.2015.09.020
PMC
PMC4688151
Cited by
42
References
1
Language
en
Licence
Funders
  • NICHD (5R00HD073269)
  • University of Georgia start up fund

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