miR-200 family controls late steps of postnatal forebrain neurogenesis via Zeb2 inhibition

被引:33
作者
Beclin, Christophe [1 ]
Follert, Philipp [1 ]
Stappers, Elke [2 ]
Barral, Serena [1 ,3 ]
Nathalie, Core [1 ]
de Chevigny, Antoine [1 ]
Magnone, Virginie [4 ,5 ]
Lebrigand, Kevin [4 ,5 ]
Bissels, Ute [3 ]
Huylebroeck, Danny [2 ,6 ]
Bosio, Andreas [3 ]
Barbry, Pascal [4 ,5 ]
Seuntjens, Eve [2 ,7 ]
Cremer, Harold [1 ]
机构
[1] Aix Marseille Univ, IBDM, CNRS, UMR7288, F-13288 Marseille, France
[2] KULeuven, Dept Dev & Regenerat, Lab Mol Biol, B-3000 Leuven, Belgium
[3] Miltenyi Biotec GmbH, Bergisch Gladbach, Germany
[4] CNRS, Sophia Antipolis, France
[5] Univ Nice Sophia Antipolis, IPMC, Sophia Antipolis, France
[6] Erasmus MC, Dept Cell Biol, NL-3015 CN Rotterdam, Netherlands
[7] Univ Liege, GIGA Neurosci, B-4000 Liege, Belgium
来源
SCIENTIFIC REPORTS | 2016年 / 6卷
关键词
E-CADHERIN; MESENCHYMAL TRANSITION; MOTILE CILIOGENESIS; BRAIN-DEVELOPMENT; REPRESSORS ZEB1; FEEDBACK LOOP; MICRORNA; CELLS; NEURONS; MIGRATION;
D O I
10.1038/srep35729
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
During neurogenesis, generation, migration and integration of the correct numbers of each neuron subtype depends on complex molecular interactions in space and time. MicroRNAs represent a key control level allowing the flexibility and stability needed for this process. Insight into the role of this regulatory pathway in the brain is still limited. We performed a sequential experimental approach using postnatal olfactory bulb neurogenesis in mice, starting from global expression analyses to the investigation of functional interactions between defined microRNAs and their targets. Deep sequencing of small RNAs extracted from defined compartments of the postnatal neurogenic system demonstrated that the miR-200 family is specifically induced during late neuronal differentiation stages. Using in vivo strategies we interfered with the entire miR-200 family in loss- and gain-of-function settings, showing a role of miR-200 in neuronal maturation. This function is mediated by targeting the transcription factor Zeb2. Interestingly, so far functional interaction between miR-200 and Zeb2 has been exclusively reported in cancer or cultured stem cells. Our data demonstrate that this regulatory interaction is also active during normal neurogenesis.
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页数:11
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