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神经模式形成过程中非蛋白水解泛素化对 Shh/Gli 信号梯度的微调。

Fine-Tuning of Shh/Gli Signaling Gradient by Non-proteolytic Ubiquitination during Neural Patterning.

机构信息

State Key Laboratory of Genetic Resources and Evolution, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming 650223, China.

State Key Laboratory of Medical Neurobiology and MOE Frontiers Center for Brain Science, Institutes of Brain Science, Fudan University, Shanghai 200032, China.

出版信息

Cell Rep. 2019 Jul 9;28(2):541-553.e4. doi: 10.1016/j.celrep.2019.06.017.

Abstract

Sonic Hedgehog (Shh) signaling plays crucial roles in patterning the ventral neural tube, which is transformed into opposing gradients of repressor and activator forms of Glis. Here, we show that the fine-tuning of the shape of the Gli gradients through non-proteolytic ubiquitination-mediated nuclear exportation plays an important role in the control of local neural cell fate. Loss of RNF220, a ventral neural-specific ubiquitin E3 ligase, leads to ventral expansion of the intermediate V0 and dorsal expansion of the ventral V3 neurons, while reducing the V1, V2, and motor neurons between them. We show that RNF220 interacts with all Glis, either in their activator or repressor forms; induces their K63-linked ubiquitination; and promotes their nuclear export, likely by unmasking a nuclear export signal in the zinc finger domain. We propose that RNF220 works to refine the Gli gradients during neural patterning by limiting the effective Gli levels in the nucleus.

摘要

Sonic Hedgehog (Shh) 信号通路在腹侧神经管的模式形成中发挥着关键作用,腹侧神经管会转化为 Glis 的抑制因子和激活因子的相反梯度。在这里,我们表明,通过非蛋白水解泛素化介导的核输出来精细调整 Gli 梯度的形状,对于控制局部神经细胞命运起着重要作用。RNF220 是一种腹侧神经特异性泛素 E3 连接酶的缺失会导致中间 V0 的腹侧扩张和腹侧 V3 神经元的背侧扩张,同时减少它们之间的 V1、V2 和运动神经元。我们表明,RNF220 与所有的 Glis 相互作用,无论是在其激活剂还是抑制剂形式下;诱导它们的 K63 连接泛素化;并促进它们的核输出,可能是通过在锌指结构域中揭示一个核输出信号。我们提出,RNF220 通过限制核内有效的 Gli 水平,在神经模式形成过程中精细调整 Gli 梯度。

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