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胎牛血清诱导有胎生黑鮶精子激活的组学研究。

Omics insights into spermatozoa activation induced by Fetal bovine serum in viviparous black rockfish (Sebastes schlegelii).

机构信息

MOE Key Laboratory of Marine Genetics and Breeding, College of Marine Life Sciences, Ocean University of China, 5 Yushan Road, Qingdao 266003, China.

MOE Key Laboratory of Marine Genetics and Breeding, College of Marine Life Sciences, Ocean University of China, 5 Yushan Road, Qingdao 266003, China; Key Laboratory of Tropical Aquatic Germplasm of Hainan Province, Sanya Oceanographic Institution, Ocean University of China, Sanya 572000, China.

出版信息

Gene. 2023 Jan 30;851:147014. doi: 10.1016/j.gene.2022.147014. Epub 2022 Oct 29.

Abstract

Black rockfish (Sebastes schlegelii) is an economically important marine species with the characteristics of viviparity. The spermatozoa were transferred into the ovary by mating and stored for several months until fertilization. Little is known about spermatozoa activation and its mechanism in black rockfish. In this study, the suitable medium for spermatozoa activation in vitro was explored, and the underlying mechanism was studied by omics analysis. Fetal bovine serum (FBS) could significantly enhance spermatozoa motility in vitro. Omics analysis showed 559 differentially expressed genes (DEGs) and 1311 differentially methylated genes (DMGs) were identified after FBS treatment. Transcriptome analysis revealed that FBS-induced spermatozoa motility activation is associated with spermatozoa capacitation regulated by the cAMP-SRC-PKA, cGMP-PKG and phospholipase D signaling pathway. Spermatozoa capacitation-related gene hsp90aa1 and chemotaxis-related gene cxcr4 were two of the important DMGs. Methylome analysis further revealed that FBS-induced epigenetic modifications are involved in spermatozoa capacitation and chemotaxis. 36 overlaps were identified between DMGs and DEGs, of which five genes were demonstrated to play a role in spermatozoa physiology, required for flagellum stability and spermatozoa motility. The results could provide new clues for understanding spermatozoa activation's molecular mechanism and help establish activation and/or immobilizing media for improving either artificial fertilization or cryopreservation in black rockfish.

摘要

黑鮶(Sebastes schlegelii)是一种具有胎生特性的重要海洋经济鱼类。其精子通过交配进入卵巢,并在那里储存数月,直到受精。目前对于黑鮶精子的激活及其机制知之甚少。本研究旨在探索体外精子激活的适宜培养基,并通过组学分析研究其潜在机制。胎牛血清(FBS)可显著增强黑鮶精子的体外活力。组学分析显示,FBS 处理后鉴定出 559 个差异表达基因(DEGs)和 1311 个差异甲基化基因(DMGs)。转录组分析表明,FBS 诱导的精子活力激活与 cAMP-SRC-PKA、cGMP-PKG 和磷脂酶 D 信号通路调节的精子顶体反应有关。精子顶体反应相关基因 hsp90aa1 和趋化相关基因 cxcr4 是两个重要的 DMGs。甲基组学分析进一步表明,FBS 诱导的表观遗传修饰参与了精子顶体反应和趋化作用。DMGs 和 DEGs 之间有 36 个重叠,其中 5 个基因在精子生理中发挥作用,对于鞭毛稳定性和精子活力是必需的。这些结果为深入了解精子激活的分子机制提供了新线索,并有助于建立激活和/或固定培养基,以提高黑鮶的人工受精或冷冻保存效果。

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