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在果蝇神经系统中,分段同源神经元获得两种不同的终端神经肽命运。

Segmentally homologous neurons acquire two different terminal neuropeptidergic fates in the Drosophila nervous system.

机构信息

Departamento de Biología, Universidad Autónoma de Madrid, Cantoblanco, Madrid, Spain.

Department of Cellular and Physiological Sciences, University of British Columbia, Vancouver, British Columbia, Canada.

出版信息

PLoS One. 2018 Apr 10;13(4):e0194281. doi: 10.1371/journal.pone.0194281. eCollection 2018.

Abstract

In this study, we identify the means by which segmentally homologous neurons acquire different neuropeptide fates in Drosophila. Ventral abdominal (Va)-neurons in the A1 segment of the ventral nerve cord express DH31 and AstA neuropeptides (neuropeptidergic fate I) by virtue of Ubx activity, whereas the A2-A4 Va-neurons express the Capa neuropeptide (neuropeptidergic fate II) under the influence of abdA. These different fates are attained through segment-specific programs of neural subtype specification undergone by segmentally homologous neurons. This is an attractive alternative by which Hox genes can shape Drosophila segmental neural architecture (more sophisticated than the previously identified binary "to live" or "not to live" mechanism). These data refine our knowledge of the mechanisms involved in diversifying neuronal identity within the central nervous system.

摘要

在这项研究中,我们确定了分段同源神经元在果蝇中获得不同神经肽命运的方式。腹神经索 A1 节段的腹侧(Va)神经元通过 Ubx 活性表达 DH31 和 AstA 神经肽(神经肽命运 I),而 A2-A4 Va 神经元在 abdA 的影响下表达 Capa 神经肽(神经肽命运 II)。这些不同的命运是通过分段同源神经元经历的神经亚型特化的分段特异性程序获得的。这是 Hox 基因塑造果蝇节段性神经结构的一种有吸引力的替代方式(比以前确定的“生存”或“不生存”的二元机制更复杂)。这些数据细化了我们对中枢神经系统内神经元身份多样化所涉及的机制的认识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1262/5892886/d9fc5fab52c7/pone.0194281.g001.jpg

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