Castor is a temporal transcription factor that specifies early born central complex neuron identity.

IF 3.7 2区 生物学 Q1 DEVELOPMENTAL BIOLOGY Development Pub Date : 2024-12-15 Epub Date: 2024-12-16 DOI:10.1242/dev.204318
Noah R Dillon, Chris Q Doe
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Abstract

The generation of neuronal diversity is important for brain function, but how diversity is generated is incompletely understood. We used the development of the Drosophila central complex (CX) to address this question. The CX develops from eight bilateral Type 2 neuroblasts (T2NBs), which generate hundreds of different neuronal types. T2NBs express broad opposing temporal gradients of RNA-binding proteins. It remains unknown whether these protein gradients are sufficient to directly generate all known neuronal diversity, or whether there are temporal transcription factors (TTFs) with narrow expression windows that each specify a small subset of CX neuron identities. Multiple candidate TTFs have been identified, but their function remains uncharacterized. Here, we show that: (1) the adult E-PG neurons are born from early larval T2NBs; (2) the candidate TTF Castor is expressed transiently in early larval T2NBs when E-PG and P-EN neurons are born; and (3) Castor is required to specify early born E-PG and P-EN neuron identities. We conclude that Castor is a TTF in larval T2NB lineages that specifies multiple, early born CX neuron identities.

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Castor是一个时间转录因子,指定早期出生的中枢复杂神经元的身份。
神经元多样性的产生对大脑功能很重要,但多样性是如何产生的还不完全清楚。我们利用果蝇中央复合体(CX)的发展来解决这个问题。CX由8个双侧2型神经母细胞(T2NBs)发育而来,产生数百种不同的神经元类型。T2NBs表达广泛相反的rna结合蛋白时间梯度。目前尚不清楚这些蛋白质梯度是否足以直接产生所有已知的神经元多样性,或者是否存在具有狭窄表达窗口的时间转录因子(ttf),每个转录因子指定CX神经元身份的一小部分。已经确定了多个候选ttf,但它们的功能尚未确定。本研究表明:(i)成体E-PG神经元来自早期t2nb幼虫;(ii)当E-PG和P-EN神经元出生时,候选TTF Castor在早期t2nb幼虫中短暂表达;(iii) Castor需要指定早期出生的E-PG和P-EN神经元身份。我们得出结论,Castor是T2NB幼虫谱系中的TTF,该谱系指定了多个早期出生的CX神经元身份。
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来源期刊
Development
Development 生物-发育生物学
CiteScore
6.70
自引率
4.30%
发文量
433
审稿时长
3 months
期刊介绍: Development’s scope covers all aspects of plant and animal development, including stem cell biology and regeneration. The single most important criterion for acceptance in Development is scientific excellence. Research papers (articles and reports) should therefore pose and test a significant hypothesis or address a significant question, and should provide novel perspectives that advance our understanding of development. We also encourage submission of papers that use computational methods or mathematical models to obtain significant new insights into developmental biology topics. Manuscripts that are descriptive in nature will be considered only when they lay important groundwork for a field and/or provide novel resources for understanding developmental processes of broad interest to the community. Development includes a Techniques and Resources section for the publication of new methods, datasets, and other types of resources. Papers describing new techniques should include a proof-of-principle demonstration that the technique is valuable to the developmental biology community; they need not include in-depth follow-up analysis. The technique must be described in sufficient detail to be easily replicated by other investigators. Development will also consider protocol-type papers of exceptional interest to the community. We welcome submission of Resource papers, for example those reporting new databases, systems-level datasets, or genetic resources of major value to the developmental biology community. For all papers, the data or resource described must be made available to the community with minimal restrictions upon publication. To aid navigability, Development has dedicated sections of the journal to stem cells & regeneration and to human development. The criteria for acceptance into these sections is identical to those outlined above. Authors and editors are encouraged to nominate appropriate manuscripts for inclusion in one of these sections.
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