• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

七喜基因在神经母细胞中发挥作用,以确定成虫中央复合体神经元身份并启动神经母细胞退役。

Seven-up acts in neuroblasts to specify adult central complex neuron identity and initiate neuroblast decommissioning.

作者信息

Dillon Noah R, Manning Laurina, Hirono Keiko, Doe Chris Q

机构信息

Institute of Neuroscience, Howard Hughes Medical Institute, University of Oregon, Eugene, OR 97403.

出版信息

bioRxiv. 2023 Nov 3:2023.11.02.565340. doi: 10.1101/2023.11.02.565340.

DOI:10.1101/2023.11.02.565340
PMID:37961302
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10635090/
Abstract

An open question in neurobiology is how diverse neuron cell types are generated from a small number of neural stem cells. In the larval central brain, there are eight bilateral Type 2 neuroblast (T2NB) lineages that express a suite of early temporal factors followed by a different set of late temporal factors and generate the majority of the central complex (CX) neurons. The early-to-late switch is triggered by the orphan nuclear hormone receptor Seven-up (Svp), yet little is known about this Svp-dependent switch in specifying CX neuron identities. Here, we (i) birthdate the CX neurons P-EN and P-FN (early and late, respectively); (ii) show that Svp is transiently expressed in all early T2NBs; and (iii) show that loss of Svp expands the population of early born P-EN neurons at the expense of late born P-FN neurons. Furthermore, in the absence of Svp, T2NBs fail decommissioning and abnormally extend their lineage into week-old adults. We conclude that Svp is required to specify CX neuron identity, as well as to initiate T2NB decommissioning.

摘要

神经生物学中的一个开放性问题是,如何从少量神经干细胞产生多种类型的神经元细胞。在幼虫的中枢脑中,有八个双侧2型神经母细胞(T2NB)谱系,它们表达一组早期时间因子,随后是另一组不同的晚期时间因子,并产生大部分中央复合体(CX)神经元。从早期到晚期的转变由孤儿核激素受体Seven-up(Svp)触发,但对于这种依赖Svp的转变在确定CX神经元身份方面的了解甚少。在这里,我们(i)确定了CX神经元P-EN和P-FN的出生日期(分别为早期和晚期);(ii)表明Svp在所有早期T2NB中短暂表达;(iii)表明Svp的缺失以牺牲晚期出生的P-FN神经元为代价,扩大了早期出生的P-EN神经元的数量。此外,在没有Svp的情况下,T2NB无法退役,并异常地将其谱系延伸到一周大的成虫中。我们得出结论,Svp对于确定CX神经元身份以及启动T2NB退役是必需的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb7c/10635090/80fe7d496085/nihpp-2023.11.02.565340v1-f0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb7c/10635090/9f33f47539ef/nihpp-2023.11.02.565340v1-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb7c/10635090/4a2e9a0db482/nihpp-2023.11.02.565340v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb7c/10635090/59e0c2249dff/nihpp-2023.11.02.565340v1-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb7c/10635090/d30d39a7b3ee/nihpp-2023.11.02.565340v1-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb7c/10635090/5e3f83c46d90/nihpp-2023.11.02.565340v1-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb7c/10635090/cd4341f7407d/nihpp-2023.11.02.565340v1-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb7c/10635090/80fe7d496085/nihpp-2023.11.02.565340v1-f0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb7c/10635090/9f33f47539ef/nihpp-2023.11.02.565340v1-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb7c/10635090/4a2e9a0db482/nihpp-2023.11.02.565340v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb7c/10635090/59e0c2249dff/nihpp-2023.11.02.565340v1-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb7c/10635090/d30d39a7b3ee/nihpp-2023.11.02.565340v1-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb7c/10635090/5e3f83c46d90/nihpp-2023.11.02.565340v1-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb7c/10635090/cd4341f7407d/nihpp-2023.11.02.565340v1-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb7c/10635090/80fe7d496085/nihpp-2023.11.02.565340v1-f0007.jpg

相似文献

1
Seven-up acts in neuroblasts to specify adult central complex neuron identity and initiate neuroblast decommissioning.七喜基因在神经母细胞中发挥作用,以确定成虫中央复合体神经元身份并启动神经母细胞退役。
bioRxiv. 2023 Nov 3:2023.11.02.565340. doi: 10.1101/2023.11.02.565340.
2
Seven-up acts in neuroblasts to specify adult central complex neuron identity and initiate neuroblast decommissioning.七上八下在神经母细胞中发挥作用,以指定成年中枢复合神经元的身份,并启动神经母细胞退役。
Development. 2024 Feb 1;151(3). doi: 10.1242/dev.202504.
3
The pipsqueak-domain proteins Distal antenna and Distal antenna-related restrict Hunchback neuroblast expression and early-born neuronal identity.微小结构域蛋白 Distal antenna 和 Distal antenna-related 限制 Hunchback 神经母细胞的表达和早期出生的神经元身份。
Development. 2011 May;138(9):1727-35. doi: 10.1242/dev.061499. Epub 2011 Mar 23.
4
seven-up Controls switching of transcription factors that specify temporal identities of Drosophila neuroblasts.七上基因控制转录因子的转换,这些转录因子决定果蝇神经母细胞的时间特性。
Dev Cell. 2005 Feb;8(2):203-13. doi: 10.1016/j.devcel.2004.12.014.
5
Timing of identity: spatiotemporal regulation of hunchback in neuroblast lineages of Drosophila by Seven-up and Prospero.身份确定的时机:七上蛋白和宝仙蛋白对果蝇神经母细胞谱系中驼背蛋白的时空调控
Development. 2006 Feb;133(3):429-37. doi: 10.1242/dev.02229. Epub 2006 Jan 5.
6
The Hunchback temporal transcription factor establishes, but is not required to maintain, early-born neuronal identity.驼背时间转录因子确立了早期生成神经元的身份,但维持该身份并非必需。
Neural Dev. 2017 Jan 31;12(1):1. doi: 10.1186/s13064-017-0078-1.
7
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。
Neural Dev. 2010 Oct 1;5:26. doi: 10.1186/1749-8104-5-26.
8
Seven up acts as a temporal factor during two different stages of neuroblast 5-6 development.七上八下在神经母细胞瘤 5-6 发育的两个不同阶段充当临时因素。
Development. 2011 Dec;138(24):5311-20. doi: 10.1242/dev.070946. Epub 2011 Nov 9.
9
From temporal patterning to neuronal connectivity in Drosophila type I neuroblast lineages.从果蝇 I 型神经母细胞谱系的时间模式到神经元连接。
Semin Cell Dev Biol. 2023 Jun;142:4-12. doi: 10.1016/j.semcdb.2022.05.022. Epub 2022 May 31.
10
Delta-dependent Notch activation closes the early neuroblast temporal program to promote lineage progression and neurogenesis termination in .Delta 依赖性的 Notch 激活关闭早期神经母细胞的时间程序,以促进谱系进展和神经发生终止。
Elife. 2024 Feb 23;12:RP88565. doi: 10.7554/eLife.88565.

本文引用的文献

1
Stem cell-specific ecdysone signaling regulates the development of dorsal fan-shaped body neurons and sleep homeostasis.干细胞特异性蜕皮激素信号调节背扇形体神经元的发育和睡眠稳态。
Curr Biol. 2024 Nov 4;34(21):4951-4967.e5. doi: 10.1016/j.cub.2024.09.020. Epub 2024 Oct 8.
2
Delta-dependent Notch activation closes the early neuroblast temporal program to promote lineage progression and neurogenesis termination in .Delta 依赖性的 Notch 激活关闭早期神经母细胞的时间程序,以促进谱系进展和神经发生终止。
Elife. 2024 Feb 23;12:RP88565. doi: 10.7554/eLife.88565.
3
The conserved RNA-binding protein Imp is required for the specification and function of olfactory navigation circuitry in Drosophila.
保守的RNA结合蛋白Imp是果蝇嗅觉导航回路的特化和功能所必需的。
Curr Biol. 2024 Feb 5;34(3):473-488.e6. doi: 10.1016/j.cub.2023.12.020. Epub 2024 Jan 4.
4
Temporal regulation of neural diversity in Drosophila and vertebrates.果蝇和脊椎动物中神经多样性的时间调控。
Semin Cell Dev Biol. 2023 Jun;142:13-22. doi: 10.1016/j.semcdb.2022.05.011. Epub 2022 May 24.
5
A connectome of the central complex reveals network motifs suitable for flexible navigation and context-dependent action selection.中央复合体的连接组揭示了适用于灵活导航和上下文依赖动作选择的网络基序。
Elife. 2021 Oct 26;10:e66039. doi: 10.7554/eLife.66039.
6
The Neuroanatomical Ultrastructure and Function of a Biological Ring Attractor.生物环吸引子的神经解剖超微结构和功能。
Neuron. 2020 Oct 14;108(1):145-163.e10. doi: 10.1016/j.neuron.2020.08.006. Epub 2020 Sep 10.
7
A large-scale resource for tissue-specific CRISPR mutagenesis in .大规模组织特异性 CRISPR 基因敲除资源库。
Elife. 2020 Feb 13;9:e53865. doi: 10.7554/eLife.53865.
8
A neural heading estimate is compared with an internal goal to guide oriented navigation.神经航向估计与内部目标进行比较,以指导有向导航。
Nat Neurosci. 2019 Sep;22(9):1460-1468. doi: 10.1038/s41593-019-0444-x. Epub 2019 Jul 22.
9
Temporal identity establishes columnar neuron morphology, connectivity, and function in a navigation circuit.时间同一性建立了导航回路中柱状神经元的形态、连接和功能。
Elife. 2019 Feb 6;8:e43482. doi: 10.7554/eLife.43482.
10
Developmentally Arrested Precursors of Pontine Neurons Establish an Embryonic Blueprint of the Drosophila Central Complex.发育停滞的脑桥神经元前体细胞建立了果蝇中枢复合体的胚胎蓝图。
Curr Biol. 2019 Feb 4;29(3):412-425.e3. doi: 10.1016/j.cub.2018.12.012. Epub 2019 Jan 17.