Meis2 is a Pax6 co-factor in neurogenesis and dopaminergic periglomerular fate specification in the adult olfactory bulb

Author:

Agoston Zsuzsa12,Heine Peer2,Brill Monika S.34,Grebbin Britta Moyo1,Hau Ann-Christin1,Kallenborn-Gerhardt Wiebke2,Schramm Jasmine1,Götz Magdalena34,Schulte Dorothea12

Affiliation:

1. Institute of Neurology (Edinger Institute), J. W. Goethe University Medical School, D-60528 Frankfurt, Germany.

2. Department of Neuroanatomy, Max-Planck-Institute for Brain Research, D-60528 Frankfurt, Germany.

3. Physiological Genomics, Institute for Physiology, Ludwig-Maximilians University Munich, D-80336 Munich, Germany.

4. Institute for Stem Cell Research, Helmholtz Zentrum München, D-85764 Neuherberg, Germany.

Abstract

Meis homeodomain transcription factors control cell proliferation, cell fate specification and differentiation in development and disease. Previous studies have largely focused on Meis contribution to the development of non-neuronal tissues. By contrast, Meis function in the brain is not well understood. Here, we provide evidence for a dual role of the Meis family protein Meis2 in adult olfactory bulb (OB) neurogenesis. Meis2 is strongly expressed in neuroblasts of the subventricular zone (SVZ) and rostral migratory stream (RMS) and in some of the OB interneurons that are continuously replaced during adult life. Targeted manipulations with retroviral vectors expressing function-blocking forms or with small interfering RNAs demonstrated that Meis activity is cell-autonomously required for the acquisition of a general neuronal fate by SVZ-derived progenitors in vivo and in vitro. Additionally, Meis2 activity in the RMS is important for the generation of dopaminergic periglomerular neurons in the OB. Chromatin immunoprecipitation identified doublecortin and tyrosine hydroxylase as direct Meis targets in newly generated neurons and the OB, respectively. Furthermore, biochemical analyses revealed a previously unrecognized complex of Meis2 with Pax6 and Dlx2, two transcription factors involved in OB neurogenesis. The full pro-neurogenic activity of Pax6 in SVZ derived neural stem and progenitor cells requires the presence of Meis. Collectively, these results show that Meis2 cooperates with Pax6 in generic neurogenesis and dopaminergic fate specification in the adult SVZ-OB system.

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

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