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

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作者
Christophe Beclin
Philipp Follert
Elke Stappers
Serena Barral
Nathalie Coré
Antoine de Chevigny
Virginie Magnone
Kévin Lebrigand
Ute Bissels
Danny Huylebroeck
Andreas Bosio
Pascal Barbry
Eve Seuntjens
Harold Cremer
机构
[1] IBDM,
[2] Aix-Marseille Université,undefined
[3] CNRS,undefined
[4] Laboratory of Molecular Biology,undefined
[5] Dept Development and Regeneration,undefined
[6] Miltenyi Biotec GmbH,undefined
[7] CNRS and University Nice Sophia Antipolis,undefined
[8] IPMC,undefined
[9] Dept Cell Biology,undefined
[10] Erasmus MC,undefined
[11] GIGA-Neurosciences,undefined
[12] Université de Liège,undefined
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摘要
During neurogenesis, generation, migration and integration of the correct numbers of each neuron sub-type 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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