FG repeats drive co-clustering of nuclear pores and P granules in the C. elegans germline.

IF 3.7 2区 生物学 Q1 DEVELOPMENTAL BIOLOGY
Development Pub Date : 2025-03-15 Epub Date: 2025-03-27 DOI:10.1242/dev.204585
Laura L Thomas, Devavrat M Bodas, Geraldine Seydoux
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引用次数: 0

Abstract

Condensates that accumulate small RNA biogenesis factors (nuage) are common in germ cells and often associate with nuclei. In the Caenorhabditis elegans germline, P granules overlay large clusters of nuclear pores and this organization has been proposed to facilitate surveillance of nascent transcripts by Argonaute proteins enriched in P granules. We report that co-clustering of nuclear pores and P granules depends on FG repeat-containing nucleoporins and FG repeats in the Vasa class helicase GLH-1. Worms with mutations that prevent this co-clustering are fertile under standard growth conditions and exhibit misregulation of only a minority of genes, including replication-dependent histones. Our observations suggest that association with nuclear pores, although non-essential for genome surveillance, may serve to tune mRNA flow through P granules and other nuage condensates.

在线虫种系中,FG重复序列驱动核孔和P颗粒的共聚。
积聚小RNA生物发生因子(nuage)的凝聚物在生殖细胞中很常见,通常与细胞核有关。在秀丽隐杆线虫的种系中,磷颗粒覆盖在核孔的大簇上,这种组织被认为是为了便于利用富含磷颗粒的Argonaute蛋白对新生转录物进行监测。我们报道了核孔和P颗粒的共同聚集取决于含有核孔蛋白的FG重复序列和Vasa类解旋酶GLH-1中的FG重复序列。阻止共聚集的突变体在标准生长条件下是可育的,并且只对少数基因(包括依赖复制的组蛋白)进行错误调控。我们的观察结果表明,与核孔的关联虽然对基因组监测不是必需的,但可能有助于调节mRNA通过P颗粒和其他核凝聚体的流动。
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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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