ROMO1是猪胚胎着床前发育过程中线粒体代谢所必需的。

IF 2.8 4区 生物学 Q3 CELL BIOLOGY Cell Division Pub Date : 2021-12-16 DOI:10.1186/s13008-021-00076-7
Dongjie Zhou, Ming-Hong Sun, Song-Hee Lee, Xiang-Shun Cui
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引用次数: 6

摘要

背景:活性氧(ROS)调节剂1 (ROMO1)是一种线粒体膜蛋白,对线粒体ROS产生和氧化还原传感的调节至关重要。ROMO1调节细胞内ROS的产生,参与细胞增殖、衰老和死亡等细胞过程。我们的目的是研究ROMO1在猪胚胎发生过程中对线粒体的影响。结果:我们发现ROMO1的高表达与猪着床前胚胎发育有关,表明ROMO1可能参与胚胎发生的进展。敲低ROMO1会破坏猪胚胎发育和囊胚质量,从而诱导ROS的产生,降低线粒体膜电位。敲低ROMO1通过破坏OPA1同工异构体的平衡,释放细胞色素c,减少ATP,诱导细胞凋亡,从而诱导线粒体功能障碍。同时,ROMO1过表达对胚胎的影响与ROMO1 KD相似。ROMO1的过表达挽救了ROMO1 kd诱导的胚胎发育缺陷、线粒体断裂和细胞凋亡。结论:ROMO1通过调节猪线粒体形态、功能和细胞凋亡,在胚胎发育中起关键作用。
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ROMO1 is required for mitochondrial metabolism during preimplantation embryo development in pigs.

Background: Reactive oxygen species (ROS) modulator 1 (ROMO1) is a mitochondrial membrane protein that is essential for the regulation of mitochondrial ROS production and redox sensing. ROMO1 regulates ROS generation within cells and is involved in cellular processes, such as cell proliferation, senescence, and death. Our purpose is to investigates the impact of ROMO1 on the mitochondria during porcine embryogenesis.

Results: We found that high expression of ROMO1 was associated with porcine preimplantation embryo development, indicating that ROMO1 may contribute to the progression of embryogenesis. Knockdown of ROMO1 disrupted porcine embryo development and blastocyst quality, thereby inducing ROS production and decreasing mitochondrial membrane potential. Knockdown of ROMO1 induced mitochondrial dysfunction by disrupting the balance of OPA1 isoforms to release cytochrome c, reduce ATP, and induce apoptosis. Meanwhile, ROMO1 overexpression showed similar effects as ROMO1 KD on the embryos. Overexpression of ROMO1 rescued the ROMO1 KD-induced defects in embryo development, mitochondrial fragmentation, and apoptosis.

Conclusions: ROMO1 plays a critical role in embryo development by regulating mitochondrial morphology, function, and apoptosis in pigs.

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来源期刊
Cell Division
Cell Division CELL BIOLOGY-
CiteScore
3.70
自引率
0.00%
发文量
5
审稿时长
>12 weeks
期刊介绍: Cell Division is an open access, peer-reviewed journal that encompasses all the molecular aspects of cell cycle control and cancer, cell growth, proliferation, survival, differentiation, signalling, gene transcription, protein synthesis, genome integrity, chromosome stability, centrosome duplication, DNA damage and DNA repair. Cell Division provides an online forum for the cell-cycle community that aims to publish articles on all exciting aspects of cell-cycle research and to bridge the gap between models of cell cycle regulation, development, and cancer biology. This forum is driven by specialized and timely research articles, reviews and commentaries focused on this fast moving field, providing an invaluable tool for cell-cycle biologists. Cell Division publishes articles in areas which includes, but not limited to: DNA replication, cell fate decisions, cell cycle & development Cell proliferation, mitosis, spindle assembly checkpoint, ubiquitin mediated degradation DNA damage & repair Apoptosis & cell death
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