MicroRNA profiling of mouse cortical progenitors and neurons reveals miR-486-5p as a regulator of neurogenesis

被引:16
|
作者
Dori, Martina [1 ,4 ]
Cavalli, Daniel [1 ]
Lesche, Mathias [2 ]
Massalini, Simone [1 ]
Alieh, Leila Haj Abdullah [1 ]
de Toledo, Beatriz Cardoso [1 ]
Khudayberdiev, Sharof [3 ]
Schratt, Gerhard [3 ,5 ]
Dahl, Andreas [2 ]
Calegari, Federico [1 ]
机构
[1] Tech Univ Dresden, Sch Med, CRTD Ctr Regenerat Therapies Dresden, Fetcherstr 105, D-01307 Dresden, Germany
[2] Tech Univ Dresden, DRESDEN Concept Genome Ctr, Ctr Mol & Cellular Bioengn CMCB, Fetcherstr 105, D-01307 Dresden, Germany
[3] Philipps Univ Marburg, Biochem Pharmacol Ctr Marburg, Inst Physiol Chem, Karl von Frisch Str 2, D-35043 Marburg, Germany
[4] Univ Modena & Reggio Emilia, Ctr Genome Res, Dept Life Sci, I-41100 Modena, Italy
[5] Swiss Fed Inst Technol, Inst Neurosci, Dept Hlth Sci & Technol, CH-8057 Zurich, Switzerland
来源
DEVELOPMENT | 2020年 / 147卷 / 09期
关键词
miRNA; Neurogenesis; miR-486a; miR-486b; Cortical development; Mouse; NUCLEAR RECEPTOR TLX; NEURAL STEM-CELLS; MAMMALIAN BRAIN; EXPRESSION; DIFFERENTIATION; BIOGENESIS; DGCR8; OVEREXPRESSION; TRANSCRIPTION; EXPANSION;
D O I
10.1242/dev.190520
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
MicroRNAs (miRNAs) are short (similar to 22 nt) single-stranded non-coding RNAs that regulate gene expression at the post-transcriptional level. Over recent years, many studies have extensively characterized the involvement of miRNA-mediated regulation in neurogenesis and brain development. However, a comprehensive catalog of cortical miRNAs expressed in a cell-specific manner in progenitor types of the developing mammalian cortex is still missing. Overcoming this limitation, here we exploited a double reporter mouse line previously validated by our group to allow the identification of the transcriptional signature of neurogenic commitment and provide the field with the complete atlas of miRNA expression in proliferating neural stem cells, neurogenic progenitors and newborn neurons during corticogenesis. By extending the currently known list of miRNAs expressed in the mouse brain by over twofold, our study highlights the power of cell type-specific analyses for the detection of transcripts that would otherwise be diluted out when studying bulk tissues. We further exploited our data by predicting putative miRNAs and validated the power of our approach by providing evidence for the involvement of miR-486 in brain development.
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页数:8
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