Integrative Omics reveals changes in the cellular landscape of peroxisome-deficient pex3 yeast cells.

IF 4.1 3区 生物学 Q2 CELL BIOLOGY
Microbial Cell Pub Date : 2025-02-20 eCollection Date: 2025-01-01 DOI:10.15698/mic2025.02.842
Tjasa Kosir, Hirak Das, Marc Pilegaard Pedersen, Ann-Kathrin Richard, Marco Anteghini, Vitor Martins Dos Santos, Silke Oeljeklaus, Ida J van der Klei, Bettina Warscheid
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Abstract

Peroxisomes are organelles that are crucial for cellular metabolism, but they also play important roles in non-metabolic processes such as signalling, stress response or antiviral defense. To uncover the consequences of peroxisome deficiency, we compared Saccharomyces cerevisiae wild-type with pex3 cells, which lack peroxisomes, employing quantitative proteomics and transcriptomics technologies. Cells were grown on acetate, a carbon source that requires peroxisomal enzymes of the glyoxylate cycle to generate energy and essential carbohydrates, and that does not repress the expression of peroxisomal genes. Our integrative omics analysis reveals that the absence of peroxisomes induces distinct responses at the level of the transcriptome and proteome. Transcripts of genes and corresponding proteins that are associated with peroxisomal β-oxidation were mostly increased in pex3 cells. In contrast, levels of peroxins were regulated at protein but not at transcript level. Membrane-bound peroxins were reduced, whereas the soluble receptors Pex5 and Pex7 were increased in abundance in pex3 cells. Interestingly, we found several non-peroxisomal transcript and proteins regulated in pex3 cells including mitochondrial proteins involved in respiration or import processes, which led to the identification of the mitochondrial pyruvate carrier Mpc1/3 as so far unnoticed transporter present in the peroxisomal membrane. Our results reveal the impact of the absence of peroxisomes in pex3 yeast cells and represent a rich resource of genes/proteins for follow-up studies to obtain a deeper understanding of peroxisome biology in a cellular context.

整合组学揭示了过氧化物酶体缺陷酵母细胞的细胞景观变化。
过氧化物酶体是对细胞代谢至关重要的细胞器,但它们在非代谢过程中也发挥重要作用,如信号传导、应激反应或抗病毒防御。为了揭示过氧化物酶体缺乏的后果,我们利用定量蛋白质组学和转录组学技术,将野生型酿酒酵母与缺乏过氧化物酶体的pex3细胞进行了比较。细胞生长在醋酸盐上,这种碳源需要乙醛酸循环的过氧化物酶来产生能量和必需的碳水化合物,并且不会抑制过氧化物酶基因的表达。我们的综合组学分析表明,过氧化物酶体的缺失在转录组和蛋白质组水平上诱导了不同的反应。在pex3细胞中,与过氧化物酶体β-氧化相关的基因和相应蛋白的转录本大多增加。相反,过氧化物水平在蛋白水平而非转录水平受到调控。膜结合过氧化物减少,而可溶性受体Pex5和Pex7在pex3细胞中丰度增加。有趣的是,我们在pex3细胞中发现了几种非过氧化物酶体转录物和蛋白质,包括参与呼吸或输入过程的线粒体蛋白质,这导致线粒体丙酮酸载体Mpc1/3被鉴定为存在于过氧化物酶体膜中迄今未被注意到的转运蛋白。我们的研究结果揭示了pex3酵母细胞中缺乏过氧化物酶体的影响,并为后续研究提供了丰富的基因/蛋白质资源,以获得对细胞背景下过氧化物酶体生物学的更深入了解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Microbial Cell
Microbial Cell Multiple-
CiteScore
6.40
自引率
0.00%
发文量
32
审稿时长
12 weeks
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