棘皮动物卵巢细胞状态的保持与对比。

IF 2.7 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecular Reproduction and Development Pub Date : 2023-12-06 DOI:10.1002/mrd.23721
Nathalie Oulhen, Shumpei Morita, Cosmo Pieplow, Thomas M. Onorato, Stephany Foster, Gary Wessel
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引用次数: 0

摘要

棘皮动物在整个生命周期中都会产生功能性配子,有些甚至超过 200 年。棘皮动物卵巢的组织学和超微结构已被描述,但这些卵巢如何发挥作用并维持高质量配子的产生仍是一个谜。在这里,我们首次展示了两个海胆物种(Strongylocentrotus purpuratus [Sp] 和 Lytechinus variegatus [Lv])和一个海星物种(Patiria miniata [Pm])成熟卵巢的单细胞 RNA 测序数据集。我们在 Sp 的卵巢中发现了 14 种细胞状态,在 Lv 的卵巢中发现了 16 种细胞状态,在海星的卵巢中发现了 13 种细胞状态。这一资源对于了解棘皮动物卵巢的结构和功能生物学特性至关重要,并能更好地为利用针对不同细胞类型的原位 RNA 杂交探针提供信息。我们将关键基因与细胞群联系起来,以验证这种方法。这一资源还有助于鉴定长期持续产生配子的干细胞,是检验年度生殖周期变化的基础,对了解这一重要门类的生殖进化至关重要。
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Conservation and contrast in cell states of echinoderm ovaries

Echinoderms produce functional gametes throughout their lifespan, in some cases exceeding 200 years. The histology and ultrastructure of echinoderm ovaries has been described but how these ovaries function and maintain the production of high-quality gametes remains a mystery. Here, we present the first single cell RNA sequencing data sets of mature ovaries from two sea urchin species (Strongylocentrotus purpuratus [Sp] and Lytechinus variegatus [Lv]), and one sea star species (Patiria miniata [Pm]). We find 14 cell states in the Sp ovary, 16 cell states in the Lv ovary and 13 cell states in the ovary of the sea star. This resource is essential to understand the structure and functional biology of the ovary in echinoderms, and better informs decisions in the utilization of in situ RNA hybridization probes selective for various cell types. We link key genes with cell clusters in validation of this approach. This resource also aids in the identification of the stem cells for prolonged and continuous gamete production, is a foundation for testing changes in the annual reproductive cycle, and is essential for understanding the evolution of reproduction of this important phylum.

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来源期刊
CiteScore
5.20
自引率
0.00%
发文量
78
审稿时长
6-12 weeks
期刊介绍: Molecular Reproduction and Development takes an integrated, systems-biology approach to understand the dynamic continuum of cellular, reproductive, and developmental processes. This journal fosters dialogue among diverse disciplines through primary research communications and educational forums, with the philosophy that fundamental findings within the life sciences result from a convergence of disciplines. Increasingly, readers of the Journal need to be informed of diverse, yet integrated, topics impinging on their areas of interest. This requires an expansion in thinking towards non-traditional, interdisciplinary experimental design and data analysis.
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