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embryonic type II neuroblasts: origin, temporal patterning, and contribution to the adult central complex.胚胎型II神经母细胞:起源、时间模式及对成体中央复合体的贡献
Development. 2017 Dec 15;144(24):4552-4562. doi: 10.1242/dev.157826. Epub 2017 Nov 20.
2
Drosophila type II neuroblast lineages keep Prospero levels low to generate large clones that contribute to the adult brain central complex.果蝇 II 型神经母细胞谱系维持 Prospero 水平低,以产生有助于成年大脑中枢复合体的大克隆。
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Combinatorial temporal patterning in progenitors expands neural diversity.祖细胞中的组合性时间模式扩展了神经多样性。
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本文引用的文献

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Temporal Patterning in the Drosophila CNS.果蝇中枢神经系统的时间模式。
Annu Rev Cell Dev Biol. 2017 Oct 6;33:219-240. doi: 10.1146/annurev-cellbio-111315-125210.
2
Steroid hormone induction of temporal gene expression in brain neuroblasts generates neuronal and glial diversity.类固醇激素诱导脑成神经细胞中的时间基因表达产生神经元和神经胶质细胞的多样性。
Elife. 2017 Apr 10;6:e26287. doi: 10.7554/eLife.26287.
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The Ets protein Pointed prevents both premature differentiation and dedifferentiation of Drosophila intermediate neural progenitors.Ets蛋白Pointed可防止果蝇中间神经祖细胞过早分化和去分化。
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4
Lineage mapping identifies molecular and architectural similarities between the larval and adult Drosophila central nervous system.谱系追踪揭示了果蝇幼虫和成虫中枢神经系统之间的分子和结构相似性。
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5
The study of the Bithorax-complex genes in patterning CCAP neurons reveals a temporal control of neuronal differentiation by Abd-B.对双胸复合体基因在CCAP神经元模式形成中的研究揭示了Abd - B对神经元分化的时间控制。
Biol Open. 2015 Aug 14;4(9):1132-42. doi: 10.1242/bio.012872.
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Neural dynamics for landmark orientation and angular path integration.地标定向和角度路径整合的神经动力学
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Optimized tools for multicolor stochastic labeling reveal diverse stereotyped cell arrangements in the fly visual system.用于多色随机标记的优化工具揭示了果蝇视觉系统中不同的刻板细胞排列。
Proc Natl Acad Sci U S A. 2015 Jun 2;112(22):E2967-76. doi: 10.1073/pnas.1506763112. Epub 2015 May 11.
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Transcriptional selectors, masters, and combinatorial codes: regulatory principles of neural subtype specification.转录选择因子、主控因子与组合密码:神经亚型特化的调控原则
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Development. 2014 Nov;141(22):4366-74. doi: 10.1242/dev.113381. Epub 2014 Oct 24.

胚胎型II神经母细胞:起源、时间模式及对成体中央复合体的贡献

embryonic type II neuroblasts: origin, temporal patterning, and contribution to the adult central complex.

作者信息

Walsh Kathleen T, Doe Chris Q

机构信息

Howard Hughes Medical Institute, Institute of Molecular Biology, and Institute of Neuroscience, University of Oregon, Eugene, OR 97403, USA.

Howard Hughes Medical Institute, Institute of Molecular Biology, and Institute of Neuroscience, University of Oregon, Eugene, OR 97403, USA

出版信息

Development. 2017 Dec 15;144(24):4552-4562. doi: 10.1242/dev.157826. Epub 2017 Nov 20.

DOI:10.1242/dev.157826
PMID:29158446
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5769626/
Abstract

neuroblasts are an excellent model for investigating how neuronal diversity is generated. Most brain neuroblasts generate a series of ganglion mother cells (GMCs) that each make two neurons (type I lineage), but 16 brain neuroblasts generate a series of intermediate neural progenitors (INPs) that each produce 4-6 GMCs and 8-12 neurons (type II lineage). Thus, type II lineages are similar to primate cortical lineages, and may serve as models for understanding cortical expansion. Yet the origin of type II neuroblasts remains mysterious: do they form in the embryo or larva? If they form in the embryo, do their progeny populate the adult central complex, as do the larval type II neuroblast progeny? Here, we present molecular and clonal data showing that all type II neuroblasts form in the embryo, produce INPs and express known temporal transcription factors. Embryonic type II neuroblasts and INPs undergo quiescence, and produce embryonic-born progeny that contribute to the adult central complex. Our results provide a foundation for investigating the development of the central complex, and tools for characterizing early-born neurons in central complex function.

摘要

神经母细胞是研究神经元多样性如何产生的优秀模型。大多数脑内神经母细胞会产生一系列神经节母细胞(GMCs),每个神经节母细胞会生成两个神经元(I型谱系),但有16个脑内神经母细胞会产生一系列中间神经祖细胞(INPs),每个中间神经祖细胞会产生4 - 6个神经节母细胞以及8 - 12个神经元(II型谱系)。因此,II型谱系类似于灵长类动物的皮质谱系,可能作为理解皮质扩张的模型。然而,II型神经母细胞的起源仍然是个谜:它们是在胚胎期还是幼虫期形成的?如果它们在胚胎期形成,其后代是否像幼虫期II型神经母细胞的后代那样填充成年中枢复合体?在这里,我们展示了分子和克隆数据,表明所有II型神经母细胞都在胚胎期形成,产生中间神经祖细胞并表达已知的时间转录因子。胚胎期II型神经母细胞和中间神经祖细胞会进入静止状态,并产生对成年中枢复合体有贡献的胚胎期出生的后代。我们的结果为研究中枢复合体的发育提供了基础,也为表征中枢复合体功能中早期出生的神经元提供了工具。