The WIRS motifs in Fat2 are required for Drosophila egg chamber rotation but not for elongation.

IF 3.7 2区 生物学 Q1 DEVELOPMENTAL BIOLOGY Development Pub Date : 2025-01-15 Epub Date: 2025-01-17 DOI:10.1242/dev.204201
Akanksha Bhatt, Valentin Ruffine, Uwe Töpfer, Jinhee Ryu, Elisabeth Fischer-Friedrich, Christian Dahmann
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Abstract

The elongation of tissues and organs is important for proper morphogenesis in animal development. In Drosophila ovaries, the elongation of egg chambers involves aligned Collagen IV fiber-like structures, a gradient of extracellular matrix stiffness and actin-based protrusion-driven collective cell migration, leading to the rotation of the egg chamber. Egg chamber elongation and rotation depend on the atypical cadherin Fat2. Fat2 contains in its intracellular region three WRC interacting receptor sequence (WIRS) motifs, which previously had been shown to bind to the WAVE regulatory complex (WRC), a conserved actin regulator. Here, we show that in fat2 mutant flies lacking the WIRS motifs, egg chambers fail to rotate and Collagen IV fiber-like structures are impaired, yet a gradient of extracellular matrix stiffness is established and egg chambers properly elongate. We conclude that the WIRS motifs are required for egg chamber rotation and that egg chamber rotation might be a prerequisite for proper formation of Collagen IV fiber-like structures. Egg chamber rotation, however, is dispensable for extracellular matrix stiffness gradient formation and for egg chamber elongation.

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Fat2中的WIRS基序是果蝇卵室旋转所必需的,但不是延长所必需的。
在动物发育过程中,组织和器官的伸长对正常的形态发生至关重要。在果蝇卵巢中,卵室的伸长涉及对齐的IV型胶原纤维样结构,细胞外基质刚度梯度和基于肌动蛋白的突出驱动的集体细胞迁移,导致卵室旋转。卵室的伸长和旋转取决于非典型钙粘蛋白Fat2。Fat2在其细胞内区域含有三个WRC相互作用受体序列(WIRS)基序,这些基序先前已被证明与WAVE调节复合体(WRC)结合,这是一种保守的肌动蛋白调节因子。在这里,我们发现在缺乏WIRS基序的fat2突变果蝇中,卵室不能旋转,胶原蛋白纤维样结构受损,但细胞外基质刚度梯度建立,卵室适当拉长。我们得出结论,WIRS基序是卵室旋转所必需的,卵室旋转可能是IV型胶原纤维样结构正确形成的先决条件。然而,卵室旋转对于细胞外基质刚度梯度的形成和卵室伸长是必不可少的。
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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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