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灵长类特异性基因 TMEM14B 标记外放射状胶质细胞,并促进皮质扩张和折叠。

The Primate-Specific Gene TMEM14B Marks Outer Radial Glia Cells and Promotes Cortical Expansion and Folding.

机构信息

State Key Laboratory of Brain and Cognitive Science, CAS Center for Excellence in Brain Science and Intelligence Technology (Shanghai), Institute of Biophysics, Chinese Academy of Sciences, Beijing 100101, China; University of Chinese Academy of Sciences, Beijing 100049, China.

BIOPIC, ICG, School of Life Sciences, Peking University, Beijing 100871, China.

出版信息

Cell Stem Cell. 2017 Nov 2;21(5):635-649.e8. doi: 10.1016/j.stem.2017.08.013. Epub 2017 Oct 12.

Abstract

Human brain evolution is associated with expansion and folding of the neocortex. Increased diversity in neural progenitor (NP) populations (such as basally located radial glia [RG], which reside in an enlarged outer subventricular zone [OSVZ]) likely contributes to this evolutionary expansion, although their characteristics and relative contributions are only partially understood. Through single-cell transcriptional profiling of sorted human NP subpopulations, we identified the primate-specific TMEM14B gene as a marker of basal RG. Expression of TMEM14B in embryonic NPs induces cortical thickening and gyrification in postnatal mice. This is accompanied by SVZ expansion, the appearance of outer RG-like cells, and the proliferation of multiple NP subsets, with proportional increases in all cortical layers and normal lamination. TMEM14B drives NP proliferation by increasing the phosphorylation and nuclear translocation of IQGAP1, which in turn promotes G1/S cell cycle transitions. These data show that a single primate-specific gene can drive neurodevelopmental changes that contribute to brain evolution.

摘要

人类大脑的进化与新皮层的扩张和折叠有关。神经祖细胞(NP)群体的多样性增加(例如基底放射状胶质[RG],位于扩大的脑室下区[OSVZ]的外部)可能有助于这种进化扩张,尽管它们的特征和相对贡献仅部分被理解。通过对分选的人类 NP 亚群进行单细胞转录组分析,我们确定了灵长类特有的 TMEM14B 基因为基底 RG 的标志物。在胚胎 NP 中表达 TMEM14B 可诱导新生小鼠皮质增厚和脑回形成。这伴随着 SVZ 的扩张,出现外 RG 样细胞,以及多个 NP 亚群的增殖,所有皮质层和正常分层的比例都增加。TMEM14B 通过增加 IQGAP1 的磷酸化和核易位来驱动 NP 增殖,这反过来又促进 G1/S 细胞周期转变。这些数据表明,单个灵长类特异性基因可以驱动神经发育变化,从而有助于大脑进化。

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