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

被引:0
|
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
来源
关键词
D O I
暂无
中图分类号
学科分类号
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.
引用
收藏
相关论文
共 21 条
  • [1] miR-200 family controls late steps of postnatal forebrain neurogenesis via Zeb2 inhibition
    Beclin, Christophe
    Follert, Philipp
    Stappers, Elke
    Barral, Serena
    Nathalie, Core
    de Chevigny, Antoine
    Magnone, Virginie
    Lebrigand, Kevin
    Bissels, Ute
    Huylebroeck, Danny
    Bosio, Andreas
    Barbry, Pascal
    Seuntjens, Eve
    Cremer, Harold
    SCIENTIFIC REPORTS, 2016, 6
  • [2] Correction: Corrigendum: miR-200 family controls late steps of postnatal forebrain neurogenesis via Zeb2 inhibition
    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
    Scientific Reports, 6
  • [3] miR-200 family controls late steps of postnatal forebrain neurogenesis via Zeb2 inhibition (vol 6, 35729, 2016)
    Beclin, Christophe
    Follert, Philipp
    Stappers, Elke
    Barral, Serena
    Core, Nathalie
    de Chevigny, Antoine
    Magnone, Virginie
    Lebrigand, Kevin
    Bissels, Ute
    Huylebroeck, Danny
    Bosio, Andreas
    Barbry, Pascal
    Seuntjens, Eve
    Cremer, Harold
    SCIENTIFIC REPORTS, 2016, 6
  • [4] miR-200 family and targets, ZEB1 and ZEB2, modulate uterine quiescence and contractility during pregnancy and labor
    Renthal, Nora E.
    Chen, Chien-Cheng
    Williams, Koriand'r C.
    Gerard, Robert D.
    Prange-Kiel, Janine
    Mendelson, Carole R.
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2010, 107 (48) : 20828 - 20833
  • [5] ZEB1, ZEB2, and the miR-200 family form a counterregulatory network to regulate CD8+ T cell fates
    Guan, Tianxia
    Dominguez, Claudia X.
    Amezquita, Robert A.
    Laidlaw, Brian J.
    Cheng, Jijun
    Henao-Mejia, Jorge
    Williams, Adam
    Flavell, Richard A.
    Lu, Jun
    Kaech, Susan M.
    JOURNAL OF EXPERIMENTAL MEDICINE, 2018, 215 (04): : 1153 - 1168
  • [6] The miR-200 family determines the epithelial phenotype of cancer cells by targeting the E-cadherin repressors ZEB1 and ZEB2
    Park, Sun-Mi
    Gaur, Arti B.
    Lengyel, Ernst
    Peter, Marcus E.
    GENES & DEVELOPMENT, 2008, 22 (07) : 894 - 907
  • [7] The miR-200 family inhibits epithelial-mesenchymal transition and cancer cell migration by direct targeting of E-cadherin transcriptional repressors ZEB1 and ZEB2
    Korpal, Manav
    Lee, Esther S.
    Hu, Guohong
    Kang, Yibin
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2008, 283 (22) : 14910 - 14914
  • [8] TBX1 targets the miR-200–ZEB2 axis to induce epithelial differentiation and inhibit stem cell properties
    Noriko Funato
    Hiromi Yanagisawa
    Scientific Reports, 12
  • [9] A Zeb2-miR-200c loop controls midbrain dopaminergic neuron neurogenesis and migration
    Shanzheng Yang
    Enrique M. Toledo
    Pedro Rosmaninho
    Changgeng Peng
    Per Uhlén
    Diogo S. Castro
    Ernest Arenas
    Communications Biology, 1
  • [10] A Zeb2-miR-200c loop controls midbrain dopaminergic neuron neurogenesis and migration
    Yang, Shanzheng
    Toledo, Enrique M.
    Rosmaninho, Pedro
    Peng, Changgeng
    Uhlen, Per
    Castro, Diogo S.
    Arenas, Ernest
    COMMUNICATIONS BIOLOGY, 2018, 1