Pcdhαc2 is required for axonal tiling and assembly of serotonergic circuitries in mice

Author:

Chen Weisheng V.12ORCID,Nwakeze Chiamaka L.12ORCID,Denny Christine A.34ORCID,O’Keeffe Sean12ORCID,Rieger Michael A.5ORCID,Mountoufaris George12ORCID,Kirner Amy12ORCID,Dougherty Joseph D.5ORCID,Hen René346ORCID,Wu Qiang7,Maniatis Tom12ORCID

Affiliation:

1. Department of Biochemistry and Molecular Biophysics, Columbia University, New York, NY 10032, USA.

2. Mortimer B. Zuckerman Mind Brain Behavior Institute, Columbia University, New York, NY 10027, USA.

3. Department of Psychiatry, Columbia University, New York, NY 10032, USA.

4. Division of Integrative Neuroscience, Research Foundation for Mental Hygiene, New York, NY 10032, USA.

5. Departments of Genetics and Psychiatry, Washington University School of Medicine, St. Louis, MO 63110, USA.

6. Departments of Neuroscience and Pharmacology, Columbia University, New York, NY 10032, USA.

7. Center for Comparative Biomedicine, Shanghai Jiao Tong University, Shanghai 200240, China.

Abstract

Pattern formation in the brain Neurons in the developing brain cooperate to build circuits. Mountoufaris et al. found that ∼50 variable protocadherin genes support a combinatorial identity code that allows millions of olfactory neuron axons to sort into ∼2000 glomeruli. Sharing olfactory receptors drives axons to one glomerulus, and protocadherin diversity allows the multiple axons to touch each other as they converge. On the other hand, Chen et al. found that a single C-type protocadherin underlies the tiled distribution of serotonergic neurons throughout the central nervous system. These neurons, which share protocadherin identity, enervate broad swaths evenly without touching neighboring neurons. Science , this issue p. 411 , p. 406

Funder

National Institute of Mental Health

National Institute of Neurological Disorders and Stroke

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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