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定量蛋白质组学鉴定男性精液中的蛋白质。

Quantitative Proteomics Identification of Seminal Fluid Proteins in Male .

机构信息

From the ‡Edward Grey Institute, Department of Zoology, University of Oxford, Oxford, UK;.

From the ‡Edward Grey Institute, Department of Zoology, University of Oxford, Oxford, UK.

出版信息

Mol Cell Proteomics. 2019 Mar 15;18(Suppl 1):S46-S58. doi: 10.1074/mcp.RA118.000831. Epub 2018 Oct 4.

Abstract

Seminal fluid contains some of the fastest evolving proteins currently known. These seminal fluid proteins (Sfps) play crucial roles in reproduction, such as supporting sperm function, and particularly in insects, modifying female physiology and behavior. Identification of Sfps in small animals is challenging, and often relies on samples taken from the female reproductive tract after mating. A key pitfall of this method is that it might miss Sfps that are of low abundance because of dilution in the female-derived sample or rapid processing in females. Here we present a new and complementary method, which provides added sensitivity to Sfp identification. We applied label-free quantitative proteomics to , male reproductive tissue - where Sfps are unprocessed, and highly abundant - and quantified Sfps before and immediately after mating, to infer those transferred during copulation. We also analyzed female reproductive tracts immediately before and after copulation to confirm the presence and abundance of known and candidate Sfps, where possible. Results were cross-referenced with transcriptomic and sequence databases to improve confidence in Sfp detection. Our data were consistent with 125 previously reported Sfps. We found nine high-confidence novel candidate Sfps, which were both depleted in mated , unmated males and identified within the reproductive tract of mated but not virgin females. We also identified 42 more candidates that are likely Sfps based on their abundance, known expression and predicted characteristics, and revealed that four proteins previously identified as Sfps are at best minor contributors to the ejaculate. The estimated copy numbers for our candidate Sfps were lower than for previously identified Sfps, supporting the idea that our technique provides a deeper analysis of the Sfp proteome than previous studies. Our results demonstrate a novel, high-sensitivity approach to the analysis of seminal fluid proteomes, whose application will further our understanding of reproductive biology.

摘要

精液中含有一些目前已知进化速度最快的蛋白质。这些精液蛋白(Sfps)在生殖中起着至关重要的作用,例如支持精子功能,特别是在昆虫中,它们可以改变雌性的生理和行为。在小动物中鉴定 Sfps 具有挑战性,通常依赖于交配后从雌性生殖道中采集的样本。这种方法的一个主要缺陷是,由于雌性样本中的稀释或雌性体内的快速处理,可能会错过丰度较低的 Sfps。在这里,我们提出了一种新的、互补的方法,该方法提供了对 Sfp 鉴定的额外敏感性。我们应用无标记定量蛋白质组学技术对 ,雄性生殖组织 - 其中 Sfps 未经处理且丰度很高 - 进行分析,并在交配前和交配后立即对 Sfps 进行定量,以推断在交配过程中转移的 Sfps。我们还分析了交配前和交配后立即的雌性生殖道,以尽可能确认已知和候选 Sfps 的存在和丰度。结果与转录组和序列数据库进行交叉参考,以提高 Sfp 检测的可信度。我们的数据与 125 种先前报道的 Sfps 一致。我们发现了 9 种高可信度的新型候选 Sfps,它们在交配后的 ,未交配的雄性中均被耗尽,并且在交配后的雌性生殖道中被识别,但在未交配的雌性中未被识别。我们还鉴定了 42 种更可能是 Sfps 的候选物,这些候选物基于其丰度、已知表达和预测特征,并且发现先前被鉴定为 Sfps 的四种蛋白质最多只是精液的次要贡献者。我们候选 Sfps 的估计拷贝数低于先前鉴定的 Sfps,这支持了我们的技术比以前的研究提供了对 Sfp 蛋白质组更深入分析的观点。我们的结果展示了一种新颖的、高灵敏度的精液蛋白质组分析方法,该方法的应用将进一步加深我们对生殖生物学的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8af5/6427238/cf6c9990fa17/zjw0021958500001.jpg

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