心肌素相关转录因子调控脊椎动物神经管闭合过程中肌动球蛋白收缩力和根尖连接重构。

IF 3.6 2区 生物学 Q1 DEVELOPMENTAL BIOLOGY
Development Pub Date : 2025-08-15 Epub Date: 2025-08-26 DOI:10.1242/dev.204681
Keiji Itoh, Olga Ossipova, Sergei Y Sokol
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引用次数: 0

摘要

心肌素相关转录因子A (Mrtfa),也被称为巨核母细胞白血病蛋白(Mkl1/MAL),与血清反应因子(Srf)联合调节肌动蛋白动态的转录,然而,Mrtfa在脊椎动物胚胎中的功能仍不清楚。在这里,我们发现Mrtfa是早期非洲爪蟾胚胎神经板折叠所必需的。Mrtfa敲除降低了神经和非神经外胚层的f -肌动蛋白水平并抑制了顶端收缩。相比之下,组成型活性Mrtfa的过表达通过重塑三细胞连接和肌球蛋白II的连接募集诱导外胚层细胞的顶端收缩。我们还在胚胎外胚层中发现了潜在的Mrtfa靶基因,这些基因编码肌动蛋白和许多肌动球蛋白网络和连接重塑的调节因子。我们的研究结果表明,Mrtfa在神经发育过程中控制形态发生运动中的作用。我们认为肌动球蛋白收缩性的调节是对mrtfa依赖性转录激活的基本细胞反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Myocardin-related transcription factor regulates actomyosin contractility and apical junction remodeling during vertebrate neural tube closure.

Myocardin-related transcription factor A (Mrtfa), also known as megakaryoblastic leukemia protein (Mkl1/MAL), associates with serum response factor (Srf) to regulate transcription in response to actin dynamics; however, the functions of Mrtfa in vertebrate embryos remain largely unknown. Here, we show that Mrtfa is required for neural plate folding in early Xenopus embryos. Mrtfa knockdown reduced F-actin levels and inhibited apical constriction in the neural and non-neural ectoderm. By contrast, overexpression of constitutively active Mrtfa induced apical constriction in ectodermal cells via remodeling of tricellular junctions and junctional recruitment of Myosin II. We also identify potential Mrtfa target genes in embryonic ectoderm that encode actins and many regulators of actomyosin networks and junction remodeling. Our findings suggest a role for Mrtfa in the control of morphogenetic movements during neurulation. We propose that the regulation of actomyosin contractility is an essential cellular response to Mrtfa-dependent transcriptional activation.

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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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