Independent control of neurogenesis and dorsoventral patterning by NKX2-2

Summary

Human neurogenesis is disproportionately protracted, lasting >10 times longer than in mice, allowing neural progenitors to undergo more rounds of self-renewing cell divisions and generate larger neuronal populations. In the human spinal cord, expansion of the motor neuron lineage is achieved through a newly evolved progenitor domain called the ventral motor neuron progenitor (vpMN) that delays and expands motor neurogenesis. This behavior of vpMNs is controlled by transcription factor NKX2-2, which in vpMNs is coexpressed with classical motor neuron progenitor (pMN) marker OLIG2. In this study, we sought to determine the molecular basis of NKX2-2-mediated extension and expansion of motor neurogenesis. We found that, unlike in mice or chicks, NKX2-2 in the human spinal cord does not repress dorsoventral patterning genes like OLIG2 However, it retains its ability to repress NEUROG2, a proneural gene that promotes exit from the cell cycle and motor neurogenesis. Interestingly, we found that ectopic expression of Tinman mutant Nkx2-2 in mouse pMNs phenocopies human vpMNs, repressing Neurog2 but not Olig2, resulting in delayed motor neurogenesis. Thus, our studies reveal that the classical patterning function of NKX2-2 that depends on its Tinman repressive domain is dissociated from NKX2-2's ability to repress NEUROG2 to control the onset and duration of motor neurogenesis in human ventral motor neuron progenitors. © 2026 Jang et al.; Published by Cold Spring Harbor Laboratory Press.

Authors Jang S, Abarinov EV, Dobkin JA, Hurley EC, Closser M, Sussel L, Wichterle H
Journal Genes & development
Publication Date 2026 Mar 2;40(5-6):384-395
PubMed 41526180
PubMed Central PMC12951754
DOI 10.1101/gad.352886.125

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