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Monitoring Stub1-Mediated Pexophagy
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缺乏ER局部化过氧素Pex23或Pex29的汉森菌多态细胞显示线粒体功能和形态的缺陷
Haiqiong Chen1, Rinse de Boer1, Arjen M Krikken1
1Molecular Cell Biology - Groningen Biomolecular Sciences and Biotechnology Institute, Nijenborgh 7, 9747 AG Groningen, The Netherlands.
Biology open
|April 29, 2024
概括
在Hansenula polymorpha中,Pex23家族蛋白质对于过氧体和脂质滴滴的形成至关重要. 它们的缺失会影响线粒体的结构和功能,影响细胞生长.
科学领域:
- 细胞生物学 细胞生物学
- 分子生物学分子生物学
- 酵母遗传学 酵母遗传学
背景情况:
- 佩克斯23家族蛋白质是参与过氧体和脂质体生物发生的内质网膜局部化因子.
- 汉塞努拉多态 (Hansenula polymorpha) 拥有四个Pex23家族成员:Pex23,Pex24,Pex29和Pex32. 这四个成员分别是Pex23,Pex24,Pex29和Pex32.
- 之前的研究表明,Pex24和Pex32是通过Peroxisome-endoplasmic网膜接触部位形成Peroxisome的重要组成部分.
研究的目的:
- 为了研究所有四种Pex23家族蛋白质缺失对Hansenula polymorpha.细胞器官的影响.
- 确定单个Pex23家族成员在过氧体,脂质滴和线粒体动态中的特定作用.
- 阐明Pex23家族蛋白质与线粒体-内分泌网膜相互作用之间的关系.
主要方法:
- 在Hansenula polymorpha中为Pex23,Pex24,Pex29和Pex32生成和分析单一删除菌株.
- 细胞器官的显微镜检查,包括真空孔,脂质滴和线粒体,在删除突变.
- 基因操纵,包括删除DNM1,以评估观察到的表型的抑制.
- 分析线粒体活动和细胞生长率.
主要成果:
- 在所有删除菌株中,真空管没有受到影响.
- 缺少Pex23或Pex29,但没有Pex24或Pex32,导致脂质滴滴数量减少.
- 线粒体被碎片化并聚集在pex23和pex29细胞中,与Fzo1水平降低和线粒体功能受损有关.
- 删除DNM1抑制了线粒体形态缺陷,并在pex23和pex29突变物中部分挽救了生长迟缓.
- 一个人工的线粒体-内等离子体网膜连接部分抑制了生长缺陷,表明有机体接触点发生了变化.
结论:
- 不同的Pex23家族成员调节器官生物发生的不同方面,Pex23和Pex29特别影响脂质滴形成.
- 佩克斯23和佩克斯29对于维护线粒体的完整性和功能至关重要,可能通过调节线粒体-内分泌网膜接触部位.
- Pex23家族在细胞组织中发挥着多方面的作用,超越过氧化体,影响脂质滴和线粒体.
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