生物
蛋白质组
细胞骨架
细胞生物学
核蛋白
染色质
胞浆
染色质重塑
细胞核
形态发生
核运输
功能(生物学)
蛋白质组学
核定位序列
突变体
核板
核心
核基质
基因表达调控
细胞命运测定
神经干细胞
作者
Florencia Merino,Lucas Miranda,Aparajita Kumar,Y Li,Deepak Kumar Sundaramoorthy,J Merl-Pham,Eva-Maria Schentarra,Clemens Steinek,Veronica Pravata,Claire Kittock,Martina Bürkle,Bob A. Hersbach,Javier Ferri Beneito,Florian Giesert,Ralf Jungmann,Louis‐Jan Pilaz,Stefanie M. Hauck,Silvia Cappello,Magdalena Götz
出处
期刊:Cell
[Cell Press]
日期:2026-06-11
卷期号:189 (16): 5026-5043.e15
标识
DOI:10.1016/j.cell.2026.05.019
摘要
Cellular differentiation and morphogenesis require the coordination between cytoskeletal remodeling and transcriptional programs, raising the question of how cytoskeletal information is conveyed to the nucleus. Here, we profile the nuclear and cytosolic proteome of human and murine neural stem cells (NSCs) and uncover abundant cytoskeletal proteins in the nucleus, including the microtubule-associated protein 1B (MAP1B), implicated in disease. We find that MAP1B shuttles to the nucleus where it interacts with the BRG1-containing chromatin remodeling complex. MAP1B's nuclear enrichment promotes NSC fate, as opposed to its cytosolic function promoting neuronal differentiation. In vivo, increasing the nuclear/cytosol ratio disrupts neuronal positioning, reminiscent of patients with MAP1B mutations. Mutant human brain organoids show aberrant MAP1B nuclear enrichment, enhanced BRG1 chromatin binding, and neuronal ectopia formation. Our study uncovers a nuclear pool of cytoskeleton-associated proteins, revealing their role in fate regulation during brain development and reshaping our understanding of neurodevelopmental disease etiology.
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