FOXG1 sequentially orchestrates subtype specification of postmitotic cortical projection neurons

Author:

Liu Junhua1ORCID,Yang Mengjie1ORCID,Su Mingzhao1ORCID,Liu Bin1ORCID,Zhou Kaixing1ORCID,Sun Congli1ORCID,Ba Ru1ORCID,Yu Baocong1ORCID,Zhang Baoshen1ORCID,Zhang Zhe1ORCID,Fan Wenxin2ORCID,Wang Kun1ORCID,Zhong Min1ORCID,Han Junhai2ORCID,Zhao Chunjie1ORCID

Affiliation:

1. Key Laboratory of Developmental Genes and Human Diseases, Ministry of Education, School of Medicine, Southeast University, Nanjing 210009, China.

2. Key Laboratory of Developmental Genes and Human Diseases, Ministry of Education, School of Life Science and Technology, Southeast University, Nanjing 210009, China.

Abstract

The mammalian neocortex is a highly organized six-layered structure with four major cortical neuron subtypes: corticothalamic projection neurons (CThPNs), subcerebral projection neurons (SCPNs), deep callosal projection neurons (CPNs), and superficial CPNs. Here, careful examination of multiple conditional knockout model mouse lines showed that the transcription factor FOXG1 functions as a master regulator of postmitotic cortical neuron specification and found that mice lacking functional FOXG1 exhibited projection deficits. Before embryonic day 14.5 (E14.5), FOXG1 enforces deep CPN identity in postmitotic neurons by activating Satb2 but repressing Bcl11b and Tbr1 . After E14.5, FOXG1 exerts specification functions in distinct layers via differential regulation of Bcl11b and Tbr1 , including specification of superficial versus deep CPNs and enforcement of CThPN identity. FOXG1 controls CThPN versus SCPN fate by fine-tuning Fezf2 levels through diverse interactions with multiple SOX family proteins. Thus, our study supports a developmental model to explain the postmitotic specification of four cortical projection neuron subtypes and sheds light on neuropathogenesis.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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