A master regulatory loop that activates genes in a temporally coordinated manner in muscle cells of ascidian embryos.

IF 3.7 2区 生物学 Q1 DEVELOPMENTAL BIOLOGY Development Pub Date : 2025-01-15 Epub Date: 2025-01-16 DOI:10.1242/dev.204382
Izumi Oda, Yutaka Satou
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Abstract

Ascidian larval muscle cells present a classic example of autonomous development. A regulatory mechanism for these cells has been extensively investigated, and the regulatory gene circuit has been documented from maternal factors to a muscle-specific gene. In the present study, we comprehensively identified genes expressed specifically in ascidian muscle cells, and found that all of them are under control of a positive regulatory loop of Tbx6-r.b and Mrf, the core circuit identified previously. We also found that several transcription factors under control of the Tbx6-r.b/Mrf regulatory loop exhibited various temporal expression profiles, which are probably important for creating functional muscle cells. These results, together with results of previous studies, provide an exhaustive view of the regulatory system enabling autonomous development of ascidian larval muscle cells. It shows that the Tbx6-r.b/Mrf regulatory loop, but not a single gene, serves a 'master' regulatory function. This master regulatory loop not only controls spatial gene expression patterns, but also governs temporal expression patterns in ascidian muscle cells.

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在海鞘胚胎的肌肉细胞中,以一种暂时协调的方式激活基因的主调控环。
海鞘幼虫肌肉细胞是自主发育的典型例子。这些细胞的调控机制已被广泛研究,从母体因素到肌肉特异性基因的调控基因回路已被记录在案。在本研究中,我们全面鉴定了在海鞘肌细胞中特异性表达的基因,发现它们都受到Tbx6-r正调控环的控制。b和Mrf,前面确定的核心电路。我们还发现几个转录因子受Tbx6-r的控制。b/Mrf调控环导致不同的时间表达谱,这可能对产生功能性肌肉细胞很重要。这些结果,连同先前的研究结果,提供了一个详尽的观点,使海鞘幼虫肌肉细胞自主发育的调控系统。结果表明,Tbx6-r。b/Mrf调控环,而不是单个基因,起着“主”调控功能。这个主调控环不仅控制着海鞘肌细胞的空间基因表达模式,而且还控制着海鞘肌细胞的时间表达模式。
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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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