Proteomic analysis of spermathecal fluid reveals factors related to long-term sperm storage in ant queens

IF 2.7 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecular Reproduction and Development Pub Date : 2024-02-02 DOI:10.1002/mrd.23733
Ayako Gotoh
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Abstract

Ant queens can maintain a large number of sperm cells for over a decade after mating at the beginning of their adult lives until they die. This sperm storage ability is prominent; however, the cellular mechanisms involved remain unclear. Sperm cells are maintained in the female sperm storage organ—the spermatheca—which supplies a suitable environment for sperm cells. To reveal the molecular basis of the long-term sperm storage mechanisms in ant queens, protein profiles enriched in the spermathecal fluid relative to the hemolymph were identified in Lasius japonicus using data-independent acquisition-based quantitative proteomics technology. Proteins related to the extracellular matrix, antioxidants, metabolic pathways, proteases, chaperones, and with uncharacterized functions were especially abundant with higher log ratio values in the spermathecal fluid relative to the hemolymph. These enriched proteins were shared with highly expressed genes previously detected by transcriptome analyses of the spermatheca in queens of Crematogaster osakensis that belong to a different subfamily than L. japonicus. It is likely that the ability for long-term sperm storage evolved early in the ant lineage. Therefore, the common proteins identified in these two ant species are possibly crucial for this ability.

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精巢液的蛋白质组分析揭示了与蚁后长期储存精子有关的因素
蚁后在成年之初交配后,可以在十多年内保持大量精子细胞,直至死亡。这种精子储存能力非常突出,但其中的细胞机制仍不清楚。精子细胞保存在雌性精子储存器官--精巢中,精巢为精子细胞提供了适宜的环境。为了揭示蚁后精子长期储存机制的分子基础,我们利用基于数据采集的定量蛋白质组学技术,鉴定了日本蚁后精巢液中相对于血淋巴富集的蛋白质谱。精囊液中与细胞外基质、抗氧化剂、代谢途径、蛋白酶、伴侣蛋白相关的蛋白质以及功能未定性的蛋白质尤其丰富,其对数值比精囊液高。这些富集的蛋白质与之前通过精巢转录组分析检测到的高表达基因共享,而这些高表达基因与日本蛙属于不同的亚科。长期储存精子的能力很可能是在蚂蚁的早期进化而来的。因此,在这两种蚂蚁中发现的共同蛋白质可能对这种能力至关重要。
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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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