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有丝分裂神经上皮细胞中 Elavl1/HuR 稳定 Dll1 mRNA。

Stabilization of Dll1 mRNA by Elavl1/HuR in neuroepithelial cells undergoing mitosis.

机构信息

Department of Molecular, Cellular and Developmental Neurobiology, Cajal Institute, IC-CSIC, 28002 Madrid, Spain.

出版信息

Mol Biol Cell. 2011 Apr 15;22(8):1227-39. doi: 10.1091/mbc.E10-10-0808. Epub 2011 Feb 23.

DOI:10.1091/mbc.E10-10-0808
PMID:21346194
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3078063/
Abstract

In the vertebrate neuroepithelium, the decision to differentiate is made by neural precursors soon after mitosis, when they are apically located. This process is controlled by lateral inhibitory signals triggered by the Delta/Notch pathway. During mitosis, the capacity of neural precursors to express the neurogenic genes Dll1 and Notch1 is maximal due to mRNA stabilization, but the mechanism controlling this process remains unknown. Here we show that Elav-like (Elavl1)/HuR becomes enriched in the cytoplasm of neuroepithelial cells undergoing mitosis and that this ribonucleoprotein interacts with the 3' untranslated region (UTR) of Dll1 mRNA. This interaction is functionally relevant because RNAi against Elavl1 reduces the stability of Dll1-3'UTR-containing transcripts in mitosis-arrested neuroepithelial cells, and Elavl1 null-mutant heterozygous mice show decreased Dll1 expression in the developing brain in vivo. We also show that RNAi against Elavl1 diminishes the capacity of brain precursors to trigger lateral inhibitory signals to their neighbors, an observation consistent with the increase in the rate of neurogenesis which can be detected in vivo in the developing retina of Elavl1 heterozygous mice. We conclude that Elavl1/HuR facilitates the exposure of vertebrate neuronal precursors to apically located Delta/Notch signals.

摘要

在脊椎动物神经上皮中,神经前体细胞在有丝分裂后不久就在顶端位置做出分化决定,此时它们受到 Delta/Notch 通路触发的侧向抑制信号的控制。在有丝分裂过程中,神经前体细胞表达神经发生基因 Dll1 和 Notch1 的能力达到最大值,这是由于 mRNA 稳定化,但控制这个过程的机制仍不清楚。在这里,我们表明 Elav 样蛋白(Elavl1)/HuR 在进行有丝分裂的神经上皮细胞的细胞质中富集,并且这种核糖核蛋白与 Dll1 mRNA 的 3'非翻译区(UTR)相互作用。这种相互作用具有功能相关性,因为针对 Elavl1 的 RNAi 会降低有丝分裂停滞的神经上皮细胞中包含 Dll1-3'UTR 的转录本的稳定性,并且 Elavl1 杂合突变体小鼠在体内显示出发育中的大脑中 Dll1 表达减少。我们还表明,针对 Elavl1 的 RNAi 会降低大脑前体细胞向其相邻细胞触发侧向抑制信号的能力,这一观察结果与体内可检测到的 Elavl1 杂合子小鼠发育中的视网膜中神经发生率增加一致。我们得出结论,Elavl1/HuR 促进了脊椎动物神经前体细胞暴露于顶端位置的 Delta/Notch 信号。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fdb/3078063/9931657e1c44/1227fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fdb/3078063/9b99984f89d9/1227fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fdb/3078063/7dda5fd3049a/1227fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fdb/3078063/2d16a6a72ead/1227fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fdb/3078063/b5733ec69642/1227fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fdb/3078063/23faf35bf87f/1227fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fdb/3078063/487fea17a451/1227fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fdb/3078063/bbc7140ae2ff/1227fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fdb/3078063/9931657e1c44/1227fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fdb/3078063/9b99984f89d9/1227fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fdb/3078063/7dda5fd3049a/1227fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fdb/3078063/2d16a6a72ead/1227fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fdb/3078063/b5733ec69642/1227fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fdb/3078063/23faf35bf87f/1227fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fdb/3078063/487fea17a451/1227fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fdb/3078063/bbc7140ae2ff/1227fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fdb/3078063/9931657e1c44/1227fig8.jpg

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